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@sabrinatoro sabrinatoro released this 06 Aug 22:14
· 123 commits to master since this release
c61e9b9

Content changes

New terms added: 600

Many of these terms are non-human animal diseases

Term
leukoencephalomyelopathy, dog (MONDO:1012450)
spinal dysraphism, dog (MONDO:1012259)
trapped neutrophil syndrome, dog (MONDO:1012383)
idiopathic hepatic fibrosis, dog (MONDO:1012102)
lower motor neuron disease, sheep (MONDO:1012170)
IRF6-related condition (MONDO:1040010)
hypoadrenocorticism, goat (MONDO:1012112)
congenital keratoconjunctivitis sicca and ichthyosiform dermatosis, dog (MONDO:1012432)
autosomal dwarfism, chicken (MONDO:1012065)
congenital myopathy with fiber-type disproportion, dog (MONDO:1012454)
primary hypothyroidism, domestic cat (MONDO:1012122)
platelet function defect, cattle (MONDO:1012216)
MTOR-related overgrowth spectrum (MONDO:0100572)
hydrallantois, water buffalo (MONDO:1012501)
nephropathy, dog (MONDO:1012186)
vertebral artery dissection (MONDO:1040011)
malignant hyperthermia, turkey (MONDO:1012144)
comedo syndrome, dog (MONDO:1012345)
acral mutilation syndrome, dog (MONDO:1012407)
photoreceptor dysplasia, dog (MONDO:1012362)
megaesophagus, horse (MONDO:1012156)
megaesophagus, domestic ferret (MONDO:1012154)
inborn error of hepatic metabolism, dog (MONDO:1012136)
polyarthritis, domestic cat (MONDO:1012218)
ocular melanosis, dog (MONDO:1012455)
rod-cone dysplasia, domestic cat (MONDO:1012247)
pyometra, dog (MONDO:1012542)
cerebellar cortical atrophy, cattle (MONDO:1012047)
complement component 4 deficiency, domestic guinea pig (MONDO:1012428)
laminitis, horse (MONDO:1012330)
renal cysts, pig (MONDO:1012342)
osteochondromatosis, pig (MONDO:1012563)
ACTH-independent adrenal Cushing syndrome, dog (MONDO:1012488)
malignant hyperthermia, dog (MONDO:1012145)
progressive cerebellar abiotrophy, pig (MONDO:1012224)
pulmonary adenomatosis, dog (MONDO:1012231)
cardiomyopathy and woolly haircoat syndrome, cattle (MONDO:1012035)
internal hydrocephalus, cattle (MONDO:1012106)
renal nephropathy, dog (MONDO:1012238)
bleeding disorder, dog (MONDO:1012027)
occipital dysplasia, dog (MONDO:1012194)
congenital mast cell tumor, cattle (MONDO:1012568)
congenital neuromuscular disease, sheep (MONDO:1012189)
calvarial hyperostotic syndrome, dog (MONDO:1012532)
laminitis, cattle (MONDO:1012331)
immunoglobulin A deficiency, dog (MONDO:1012130)
myoclonus epilepsy of Lafora, dog (MONDO:1012178)
atopy, domestic cat (MONDO:1012018)
sebaceous gland dysplasia, domestic cat (MONDO:1012438)
perosomus elumbis, dog (MONDO:1012207)
upper airway syndrome, dog (MONDO:1012478)
cancer, dog (MONDO:1012570)
cytochrome B-related exercise intolerance, sheep (MONDO:1012546)
idiopathic congenital chondrodystrophy, cattle (MONDO:1012465)
linear IgA disease, dog (MONDO:1012368)
vitamin D-deficiency rickets, non-type I, non-type II, domestic cat (MONDO:1012423)
bleeding disorder, domestic cat (MONDO:1012028)
EN1-related dorsoventral syndrome (MONDO:1040032)
retained placenta, cattle (MONDO:1012553)
congenital lethal spasms, cattle (MONDO:1012251)
tetragametic chimerism, water buffalo (MONDO:1012082)
alloimmune hemolytic anemia of the newborn, domestic cat (MONDO:1012006)
mitochondrial fission encephalopathy, dog (MONDO:1012561)
progressive ataxia, cattle (MONDO:1012289)
persistent right aortic arch with subclavian artery and ligamentum arteriosum, dog (MONDO:1012417)
retinal dysplasia and internal hydrocephalus, cattle (MONDO:1012429)
Laron dwarfism, cattle (MONDO:1012365)
compulsive disorder, dog (MONDO:1012411)
hemangiosarcoma, orange-winged Amazon parrot (MONDO:1012458)
laryngeal paralysis, cattle (MONDO:1012324)
primary open angle glaucoma, dog (MONDO:1012498)
reduced glutathione deficiency due to amino-acid transport defect, sheep (MONDO:1012336)
familial thoracic aortic aneurysm, dog (MONDO:1012381)
dysphagia-associated muscular dystrophy, dog (MONDO:1012173)
osteodystrophy, cattle (MONDO:1012204)
reduced glutathione deficiency, dog (MONDO:1012337)
PIK3R2-related overgrowth spectrum (MONDO:1040004)
immune-mediated myositis, horse (MONDO:1012518)
shivers, horse (MONDO:1012172)
gluten-sensitive enteropathy, dog (MONDO:1012343)
self-mutilation syndrome, horse (MONDO:1012308)
arthritis deformans, pig (MONDO:1012013)
primary ciliary dyskinesia, pig (MONDO:1012140)
tremor, pig (MONDO:1012281)
hemangiosarcoma, sheep (MONDO:1012464)
craniomandibular osteopathy, dog (MONDO:1012054)
renal amyloidosis, cattle (MONDO:1012011)
polled and multisystemic syndrome, cattle (MONDO:1012444)
immunoglobulin G2 deficiency, cattle (MONDO:1012134)
muscular dystrophy-dystroglycanopathy (limb-girdle), domestic cat (MONDO:1012427)
atopy, dog (MONDO:1012017)
congenital copper deficiency, goat (MONDO:1012053)
malignant melanoma, lion (MONDO:1012443)
tapetal degeneration, dog (MONDO:1012263)
ocular-skeletal dysplasia, dog (MONDO:1012063)
warts between hooves, cattle (MONDO:1012286)
pentalogy of Fallot, dog (MONDO:1012469)
congenital muscular dystrophy without intellectual disability (MONDO:1040033)
dermal allergy, horse (MONDO:1012060)
nephropathy, pig (MONDO:1012187)
thrombopathia, pig (MONDO:1012274)
turning calves syndrome, cattle (MONDO:1012522)
hyperkinesis, dog (MONDO:1012107)
digital dermatitis, cattle (MONDO:1012531)
tremor, domestic cat (MONDO:1012280)
reduced glutathione deficiency, sheep (MONDO:1012339)
premature senesence, rabbit (MONDO:1012326)
idiopathic hepatic fibrosis, cattle (MONDO:1012103)
osteochondroma causing progressive posterior paresis, dog (MONDO:1012201)
bone spavin, red deer (MONDO:1012335)
dystrophic epidermolysis bullosa, dog (MONDO:1012068)
neuronal vacuolar disorder, dog (MONDO:1012360)
spastic paresis, pig (MONDO:1012252)
progressive rod-cone degeneration, dog (MONDO:1012359)
sebaceous adenitis, dog (MONDO:1012415)
polyneuropathy, dog (MONDO:1012354)
neurological syndrome, dog (MONDO:1012191)
calvarial hyperostotic syndrome, lion (MONDO:1012533)
cavitating leukodystrophy, dog (MONDO:1012530)
facial dysplasia syndrome, cattle (MONDO:1012510)
internal hydrocephalus, dog (MONDO:1012105)
spina bifida with myelomeningocele, cattle (MONDO:1012256)
Laron dwarfism, pig (MONDO:1012364)
androgen insensitivity syndrome, pig (MONDO:1012267)
peripheral axonopathy, domestic cat (MONDO:1012024)
exfoliative cutaneous lupus erythematosus, dog (MONDO:1012422)
hypoadrenocorticism, domestic cat (MONDO:1012110)
Kurosawa and Kusanagi hypercholesterolaemia, rabbit (MONDO:1012416)
hypoadrenocorticism, horse (MONDO:1012111)
hemangiosarcoma, cattle (MONDO:1012463)
gyrate atrophy of choroid and retina, domestic cat (MONDO:1012447)
hypotrichosis with short life expectancy, domestic cat (MONDO:1012489)
tibial dyschondroplasia, chicken (MONDO:1012275)
cerebellar abiotrophy, domestic cat (MONDO:1012039)
congenital hypomyelinogenesis, dog (MONDO:1012114)
cervical vertebral compressive myelopathy, dog (MONDO:1012479)
persistent truncus arteriosus with ventricular septal defect and patent foramen ovale, cattle (MONDO:1012327)
myoclonus epilepsy of Lafora, Eurasian elk (MONDO:1012180)
neuroaxonal dystrophy with cerebellar abiotrophy, domestic cat (MONDO:1012421)
alpha fucosidosis, dog (MONDO:1012087)
lethal arthrogryposis syndrome, cattle (MONDO:1012491)
displaced abomasum, sheep (MONDO:1012300)
primary hypoadrenocorticism, dog (MONDO:1012113)
androgen insensitivity syndrome, horse (MONDO:1012266)
follicular dysplasia and interface dermatitis, dog (MONDO:1012375)
ventricular arrhythmias and sudden death, dog (MONDO:1012285)
degenerative myeloencephalopathy, horse (MONDO:1012309)
laryngeal paralysis, dog (MONDO:1012322)
dystrophic epidermolysis bullosa, goat (MONDO:1012071)
renal insufficiency, dog (MONDO:1012237)
hemolytic uremic syndrome, dog (MONDO:1012100)
subacute necrotising encephalopathy of Leigh, dog (MONDO:1012292)
invasive transitional cell carcinoma, dog (MONDO:1012404)
megaesophagus, cattle (MONDO:1012158)
tetragametic chimerism, bighorn sheep (MONDO:1012081)
congenital hydranencephaly and cerebellar hypoplasia, cattle (MONDO:1012435)
immunodeficiency disease, domestic cat (MONDO:1012126)
neuronal abiotrophy, dog (MONDO:1012310)
congenital stationary night blindness, LRIT3-related, dog (MONDO:1011262)
spontaneous cardiomyopathy, turkey (MONDO:1012036)
hemolytic uremic syndrome, cattle (MONDO:1012101)
bleeding disorder, pig (MONDO:1012029)
pentalogy of Fallot, horse (MONDO:1012470)
multiple exostoses, dog (MONDO:1012073)
fibrodysplasia ossificans, dog (MONDO:1012078)
mitral valve dysplasia, horse (MONDO:1012557)
chronic myelogenous leukemia, dog (MONDO:1012405)
androgen insensitivity syndrome, cattle (MONDO:1012268)
ocular squamous cell carcinoma, cattle (MONDO:1012197)
congential hepatic fibrosis, dog (MONDO:1012543)
hemangiosarcoma, African hunting dog (MONDO:1012459)
ocular squamous cell carcinoma, goat (MONDO:1012198)
primary autoimmune hemolytic anemia, dog (MONDO:1012098)
methicillin-susceptible staphylococcus aureus infectious disease (MONDO:1040020)
displaced abomasum, cattle (MONDO:1012299)
displaced abomasum, water buffalo (MONDO:1012298)
cancer, pig (MONDO:1012572)
axonopathy, cattle (MONDO:1012295)
verrucous epidermal keratinocytic nevi, domestic cat (MONDO:1012514)
congenital dyserythropoietic anemia with dyskeratosis and progressive alopecia, cattle (MONDO:1012067)
spinal dysmyelination, cattle (MONDO:1012341)
retinal degeneration, Smoky Joe, chicken (MONDO:1012474)
chronic interstitial nephropathy, ducks (MONDO:1012050)
generalized myoclonic epilepsy with photosensitivity, dog (MONDO:1012511)
perosomus elumbis, cattle (MONDO:1012210)
nasal parakeratosis, dog (MONDO:1012377)
corneal sequestra, domestic cat (MONDO:1012566)
malignant hyperthermia, pig (MONDO:1012148)
combined deficiency of factors VIII, IX, and X, horse (MONDO:1012493)
delta 9-tetrahydrocannabinol seizure, rabbit (MONDO:1012059)
white skin color and iridophoroma, leopard gecko (MONDO:1012540)
esophageal motility disorder, dog (MONDO:1012200)
diffuse cystic renal dysplasia and hepatic fibrosis, dog (MONDO:1012524)
idiopathic hypercalciuria, dog (MONDO:1012541)
hydrallantois, goat (MONDO:1012504)
hemangiosarcoma, cockatiel (MONDO:1012457)
osteodystrophy, domestic cat (MONDO:1012203)
GBA1-related Parkinson disease, susceptibility (MONDO:1040030)
alpha fucosidosis, domestic cat (MONDO:1012088)
osseous choristoma of the ciliary body, domestic guinea pig (MONDO:1012567)
hyperornithinemia, hyperammonemia, and homocitrullinuria syndrome, horse (MONDO:1012353)
lacrimal fistula, cattle (MONDO:1012436)
Mollaret’s meningitis (MONDO:1030004)
cerebellar cortical atrophy, domestic cat (MONDO:1012046)
megakaryoblastic leukemia, dog (MONDO:1012152)
congenital erythropoietic porphyria, pig (MONDO:1012313)
central retinal degeneration, domestic cat (MONDO:1012240)
ear necrosis syndrome, pig (MONDO:1012439)
immunodeficiency disease, llama (MONDO:1012127)
stomach ulcer, pig (MONDO:1012284)
spinal dysplasia, domestic cat (MONDO:1012258)
cardiomyopathy and juvenile mortality, dog (MONDO:1012535)
anal furunculosis, dog (MONDO:1012418)
nodular dermatofibrosis and kidney disease, dog (MONDO:1012318)
hypomyelinating leukodystrophy, dog (MONDO:1012539)
cerebellar Purkinje cell degeneration, dog (MONDO:1012037)
high-frequency tremor, macaques (MONDO:1012319)
cerebellar disease, cattle (MONDO:1012049)
tetragametic chimerism, cattle (MONDO:1012085)
stomatocytosis and gastrits, dog (MONDO:1012316)
motor neuron disease, dog (MONDO:1012311)
facial digital syndrome, cattle (MONDO:1012076)
progressive spinal myelopathy, cattle (MONDO:1012229)
hypocatalasia, dog (MONDO:1012305)
spina bifida with raduschisis, domestic cat (MONDO:1012257)
persistent right aortic arch, horse (MONDO:1012215)
spinal intradural arachnoid cyst, dog (MONDO:1012486)
megaesophagus, dog (MONDO:1012153)
gastric dilatation volvulus syndrome, lesser panda (MONDO:1012092)
hydrallantois, horse (MONDO:1012502)
malignant hyperthermia, rabbit (MONDO:1012151)
congenital cerebellar anomaly, pig (MONDO:1012044)
blindness with enlarged globe, chicken (MONDO:1012374)
polyneuropathy, domestic cat (MONDO:1012355)
degenerative encephalopathy, dog (MONDO:1012506)
black hair follicular dysplasia, cattle (MONDO:1012026)
hemophagocytic syndrome, dog (MONDO:1012332)
congenital myasthenic syndrome 4 (MONDO:1040021)
growth-hormone-receptor deficiency dwarfism, cattle (MONDO:1012356)
osteochondromatosis, horse (MONDO:1012562)
necrosis of digits, dog (MONDO:1012430)
PI4KA-related disorder (MONDO:1040012)
subacute necrotising encephalopathy of Leigh, cattle (MONDO:1012293)
retinal dysplasia, dog (MONDO:1012241)
nephropathy, sheep (MONDO:1012188)
Meckel-like hepatorenal fibrocystic dysplasia syndrome, sheep (MONDO:1012525)
megaesophagus, llama (MONDO:1012157)
myasthenia, dog (MONDO:1012175)
congenital melanoma, pig (MONDO:1012162)
brachygnathia, cardiomegaly and renal hypoplasia syndrome, sheep (MONDO:1012420)
persistent right aortic arch, domestic cat (MONDO:1012213)
bilateral deafness and vestibular dysfunction, dog (MONDO:1012520)
hypocatalasia, domestic guinea pig (MONDO:1012304)
growth-hormone deficiency dwarfism, zebu cattle (MONDO:1012394)
hydrallantois, cattle (MONDO:1012503)
facial eczema, sheep (MONDO:1012347)
polyarthritis, dog (MONDO:1012217)
naked foal syndrome, horse (MONDO:1012512)
Ehlers-Danlos syndrome, classic-like, 3 (MONDO:0971044)
dystrophic epidermolysis bullosa, cattle (MONDO:1012070)
PIK3CA-related overgrowth spectrum (MONDO:1040002)
micromelia, Japanese quail (MONDO:1012165)
recessive hypotrichosis, dog (MONDO:1012348)
alloxan-diabetes, dog (MONDO:1012008)
pulmonary hypoplasia with anasarca, cattle (MONDO:1012414)
unilateral subcortical heterotopia, California sea lion (MONDO:1012388)
progressive ataxia with degenerative thoracic myelopathy, sheep (MONDO:1012016)
cerebellar abiotrophy, goat (MONDO:1012042)
Guillain-Barr-like polyradiculoneuropathy, domestic cat (MONDO:1012508)
malignant hyperthermia, domestic cat (MONDO:1012146)
laryngeal paralysis, horse (MONDO:1012323)
attention deficit hyperactivity disorder, dog (MONDO:1012476)
tetragametic chimerism, sheep (MONDO:1012086)
degenerative myopathy of deep pectoral muscle, turkey (MONDO:1012057)
recurrent inflammatory pulmonary disease, dog (MONDO:1012529)
acrochordonous plaque, dog (MONDO:1012376)
audiogenic seizure, rabbit (MONDO:1012020)
rod-cone degeneration, domestic guinea pig (MONDO:1012244)
stringhalt, cattle (MONDO:1012262)
hemangiosarcoma, horse (MONDO:1012461)
neonatal hepatitis, dog (MONDO:1012291)
micromelia, ducks (MONDO:1012163)
congenital hypomyelinogenesis, cattle (MONDO:1012116)
mitral valve dysplasia, ass (MONDO:1012556)
reduced glutathione deficiency due to GCS deficiency, sheep (MONDO:1012234)
neurodegenerative vacuolar storage disease, dog (MONDO:1012492)
stringhalt, horse (MONDO:1012261)
congenital hypomyelinogenesis, pig (MONDO:1012115)
ocular squamous cell carcinoma, horse (MONDO:1012196)
Ancon dwarfism, sheep (MONDO:1012064)
cutaneous malignant melanoma in Sinclair swine, pig (MONDO:1012161)
polycystic mononephrosis, dog (MONDO:1012219)
myoclonus epilepsy of Lafora, cattle (MONDO:1012181)
megaesophagus, domestic cat (MONDO:1012155)
neonatal encephalopathy with seizures, dog (MONDO:1012392)
persistent right aortic arch, puma (MONDO:1012214)
immunoglobulin M deficiency, horse (MONDO:1012135)
subclinical hypocalcemia, cattle (MONDO:1012499)
myasthenia, domestic cat (MONDO:1012176)
degenerative myopathy of obturator-externus, dog (MONDO:1012058)
cerebellar abiotrophy, sheep (MONDO:1012043)
episodic falling, dog (MONDO:1012419)
cervical vertebral compressive myelopathy, mountain zebra (MONDO:1012480)
Hodgkin disease, dog (MONDO:1012104)
congenital hypoplasia of mammary gland, sheep (MONDO:1012118)
primary hypothyroidism, dog (MONDO:1012121)
spastic paresis, cattle (MONDO:1012253)
neurogenic muscular atrophy, dog (MONDO:1012190)
pulmonary adenomatosis, cattle (MONDO:1012232)
dyneinopathy (MONDO:1040031)
congenital myasthenic syndrome, CHAT-related, dog (MONDO:1011029)
yellow-semen syndrome, turkey (MONDO:1012361)
recurrent airway obstruction, horse (MONDO:1012386)
hemolytic anemia, cattle (MONDO:1012096)
progressive retinal atrophy, dog (MONDO:1012226)
sarcoid, horse (MONDO:1012249)
hemangiosarcoma, pig (MONDO:1012462)
mitochondrial myopathy, dog (MONDO:1012182)
renal disease, dog (MONDO:1012235)
tibial dyschondroplasia, turkey (MONDO:1012276)
pulmonary surfactant metabolism dysfunction, dog (MONDO:1012534)
subacute progressive myopathy, dog (MONDO:1012183)
degenerative suspensory ligament desmitis, horse (MONDO:1012509)
melanoblastoma, pig (MONDO:1012366)
premature senesence, pig (MONDO:1012325)
retinal and skeletal dysplasia, dog (MONDO:1012317)
neonatal pancytopenia, cattle (MONDO:1012413)
neuropathy and feather color dilution, Northern goshawk (MONDO:1012544)
high-frequency tremor, pig (MONDO:1012320)
proportionate dwarfism with inflammatory lesions, cattle (MONDO:1012433)
recessive hypotrichosis, pig (MONDO:1012349)
multiple lipomatosis, cattle (MONDO:1012143)
primary ciliary dyskinesia, domestic cat (MONDO:1012139)
familial convulsions and ataxia, cattle (MONDO:1012344)
reduced glutathione deficiency, goat (MONDO:1012338)
anal gland disease, dog (MONDO:1012558)
rod-cone degeneration, domestic cat (MONDO:1012245)
hepatocellular fibrinogen storage disease, cattle (MONDO:1012569)
progressive ataxia, pig (MONDO:1012288)
immunoglobulin G deficiency, horse (MONDO:1012133)
hypertrophic neuropathy, dog (MONDO:1012108)
alloimmune hemolytic anemia of the newborn, horse (MONDO:1012007)
chronic valvular disease, dog (MONDO:1012340)
contractural arachnodactyly, cattle (MONDO:1012403)
dystrophic epidermolysis bullosa, domestic cat (MONDO:1012069)
vitreous degeneration, dog (MONDO:1012547)
cervical vertebral compressive myelopathy, sheep (MONDO:1012482)
llama syndrome chondrodysplasia, sheep (MONDO:1012424)
myopathy of the diaphragmatic muscles, cattle (MONDO:1012363)
aniridia with cataract, horse (MONDO:1012012)
hypopigmentation and deafness, pig (MONDO:1012537)
exercise-induced pulmonary hemorrhage, horse (MONDO:1012483)
goldenhar syndrome, domestic cat (MONDO:1012516)
zinc deficiency-like syndrome, cattle (MONDO:1012487)
necrotising myelopathy, dog (MONDO:1012185)
malignant hyperthermia, cattle (MONDO:1012150)
hypothalamic dysplasia, dog (MONDO:1012119)
imperforate hymen, horse (MONDO:1012296)
verrucous epidermal keratinocytic nevi, dog (MONDO:1012513)
caprine-like generalized hypoplasia syndrome, cattle (MONDO:1012402)
type 2 polysaccharide storage myopathy, horse (MONDO:1012412)
disproportionate short-limbed chondrodysplasia, dog (MONDO:1012477)
protein C deficiency, horse (MONDO:1012230)
mitral valve disease, dog (MONDO:1012166)
cerebellar abiotrophy, cattle (MONDO:1012041)
non-specific digestive disorder, rabbit (MONDO:1012446)
early retinal degeneration, dog (MONDO:1012358)
cancer, domestic cat (MONDO:1012571)
congenital hypotrichosis with thymic aplasia, domestic cat (MONDO:1012123)
cutaneous papillomatosis, cattle (MONDO:1012307)
postpartum dysgalactia syndrome, pig (MONDO:1012467)
exercise-induced collapse, dog (MONDO:1012389)
dermatosis vegetans, pig (MONDO:1012061)
familial episodic spinocerebellar ataxia, sheep (MONDO:1012441)
congenital dyserythropoietic anemia, cattle (MONDO:1012538)
immunodeficiency disease, dog (MONDO:1012125)
lethal multi-organ developmental dysplasia, cattle (MONDO:1012440)
muscular dystrophy-dystroglycanopathy (limb-girdle), chicken (MONDO:1012426)
bone spavin, horse (MONDO:1012334)
perosomus elumbis, pig (MONDO:1012209)
paroxysm, chicken (MONDO:1012206)
malignant melanoma, dog (MONDO:1012442)
renal amyloidosis, dog (MONDO:1012009)
spontaneous autoimmune thyroiditis, domestic cat (MONDO:1012022)
rupture of the cranial cruciate ligament, dog (MONDO:1012395)
ocular squamous cell carcinoma, sheep (MONDO:1012199)
progressive retinal atrophy, domestic cat (MONDO:1012227)
Sharpin-related autoinflammatory syndrome (MONDO:1040029)
anal sac gland carcinoma, dog (MONDO:1012399)
juvenile with age-dependent emphysema hypotrichosis, pig (MONDO:1012387)
hemangiosarcoma, domestic cat (MONDO:1012460)
tetragametic chimerism, pig (MONDO:1012084)
inherited periodic spasticity, cattle (MONDO:1012385)
neurodevelopmental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities (MONDO:0971043)
myoclonus epilepsy of Lafora, domestic cat (MONDO:1012179)
segmental axonopathy, sheep (MONDO:1012398)
hypochondroplastic dwarfism, dog (MONDO:1012357)
renal dysplasia and bladder aplasia-hypoplasia, sheep (MONDO:1012236)
congenital erythropoietic porphyria, domestic cat (MONDO:1012312)
congenital blindness, pig (MONDO:1012031)
asymmetrical occipital condylar dysplasia, sheep (MONDO:1012549)
sarcoid, ass (MONDO:1012248)
myelin oligodendrocyte glycoprotein antibody-associated disease (MONDO:1040024)
dyserythropoietic anemia and myopathy syndrome, dog (MONDO:1012565)
polymicrogyria and asymmetrical ventricular dilation, dog (MONDO:1012294)
bleeding disorder, cattle (MONDO:1012030)
gastric dilatation volvulus syndrome, domestic guinea pig (MONDO:1012089)
amelogenesis imperfecta, ACP4-related, dog (MONDO:1011209)
myoclonus epilepsy of Lafora, fennec fox (MONDO:1012177)
degenerative myelopathy, dog (MONDO:1012056)
distal axonopathy, domestic cat (MONDO:1012023)
retinal dysplasia and persistent primary vitreous, dog (MONDO:1012382)
contact activation defect, domestic cat (MONDO:1012052)
juvenile idiopathic epilepsy, horse (MONDO:1012445)
laminitis, ass (MONDO:1012329)
renal cystadenocarcinoma and nodular dermatofibrosis, dog (MONDO:1012369)
skeletal dysplasia with craniofacial deformity and disproportionate dwarfism, sheep (MONDO:1012485)
anal gland disease, domestic cat (MONDO:1012559)
cerebellar cortical atrophy, sheep (MONDO:1012048)
cyclic neutropenia, dog (MONDO:1012055)
masticatory muscle myositis, dog (MONDO:1012303)
cerebellar abiotrophy, dog (MONDO:1012038)
gallbladder mucocele, dog (MONDO:1012409)
dysplastic gangliocytoma of the cerebellum, domestic cat (MONDO:1012560)
cerebral artery stenosis (MONDO:1040016)
bilateral deafness and vestibular dysfunction, pig (MONDO:1012521)
brachycephalic airway obstruction syndrome, domestic cat (MONDO:1012033)
persistent right aortic arch, dog (MONDO:1012212)
lymphoproliferative disease, dog (MONDO:1012380)
multiple exostoses, pig (MONDO:1012075)
fluoroquinolone-induced retinal degeneration, domestic cat (MONDO:1012437)
bilateral corneal stromal loss, horse (MONDO:1012526)
imperforate hymen, cattle (MONDO:1012297)
primary autoimmune hemolytic anemia, horse (MONDO:1012099)
spinal dysraphism, cattle (MONDO:1012260)
alloimmune hemolytic anemia of the newborn, dog (MONDO:1012005)
androgen insensitivity syndrome, domestic cat (MONDO:1012265)
necrotizing meningoencephalitis, dog (MONDO:1012391)
progressive neuronopathy, dog (MONDO:1012351)
autosomal T cell-negative, B cell-negative, NK cell-positive severe combined immunodeficiency disease with sensitivity to ionizing radiation, pig (MONDO:1012494)
reactive perforating collagenosis, domestic cat (MONDO:1012396)
hereditary pancreatitis, dog (MONDO:1012378)
lower motor neuron disease, pig (MONDO:1012169)
congenital merosin-deficient muscular dystrophy, domestic cat (MONDO:1012425)
sensory ataxic neuropathy, dog (MONDO:1012390)
retinal dysplasia and degeneration, chicken (MONDO:1012373)
pentalogy of Fallot, sheep (MONDO:1012471)
progressive axonopathy, dog (MONDO:1012223)
tremor, dog (MONDO:1012279)
multiple lipomatosis, pig (MONDO:1012142)
thrombopathia, dog (MONDO:1012273)
hoof wall separation syndrome, horse (MONDO:1012484)
primary ciliary dyskinesia, dog (MONDO:1012138)
multiple exostoses, horse (MONDO:1012074)
hemolytic anemia, dog (MONDO:1012095)
amelogenesis imperfecta, ENAM-related, dog (MONDO:1011202)
congenital erythropoietic porphyria, zebu cattle (MONDO:1012315)
cerebellar abiotrophy, horse (MONDO:1012040)
gastric dilatation volvulus syndrome, maned wolf (MONDO:1012090)
ichthyosis fetalis, sheep (MONDO:1012527)
type-II collagen-immune complex arthritis, sheep (MONDO:1012014)
cutaneous and renal vasculopathy, dog (MONDO:1012328)
renal amyloidosis, domestic cat (MONDO:1012010)
thrombasthenia, horse (MONDO:1012272)
osteodystrophy, rabbit (MONDO:1012205)
multiple autoimmune diseases syndrome, dog (MONDO:1012456)
protein-losing nephropathy, dog (MONDO:1012367)
malignant hyperthermia, deer (MONDO:1012149)
congenital joint laxity and dwarfism, cattle (MONDO:1012137)
mitral valve dysplasia, domestic cat (MONDO:1012555)
congenital stationary night blindness, TRPM1-related, horse (MONDO:1011255)
symmetrical onychomadesis, dog (MONDO:1012495)
pentalogy of Fallot, Amur tiger (MONDO:1012468)
hypothyroidism and dwarfism, Sumatran tiger (MONDO:1012120)
congenital erythropoietic porphyria, cattle (MONDO:1012314)
medial coronoid disease, dog (MONDO:1012473)
immunoglobulin G deficiency, chicken (MONDO:1012131)
polioencephalomyelopathy, dog (MONDO:1012350)
cervical vertebral compressive myelopathy, horse (MONDO:1012481)
brachycephalic airway obstruction syndrome, dog (MONDO:1012032)
squamous cell carcinoma of the digit, dog (MONDO:1012449)
glomerulonephropathy, dog (MONDO:1012093)
growth-hormone deficiency dwarfism, dog (MONDO:1012393)
metastatic malignant neoplasm in the brain (MONDO:1040026)
progressive retinal atrophy, sheep (MONDO:1012228)
growth and respiratory lethal syndrome, cattle (MONDO:1012564)
central retinal degeneration, cheetah (MONDO:1012239)
choroid plexus tumour, dog (MONDO:1012545)
olivopontocerebellar degeneration, domestic cat (MONDO:1012550)
recurrent uveitis, horse (MONDO:1012475)
thalamic-cerebellar neuropathy, sheep (MONDO:1012193)
immunoglobulin A deficiency, gray wolf (MONDO:1012129)
congenital myasthenic syndrome, COLQ-related, dog (MONDO:1010932)
urticaria pigmentosa, domestic cat (MONDO:1012352)
pyknodysostosis, domestic cat (MONDO:1012573)
hypotrophic axonopathy, Japanese quail (MONDO:1012124)
muscle contracture and chondrodysplasia, cattle (MONDO:1012171)
lethal acrodermatitis, dog (MONDO:1012519)
myasthenia, Amur tiger (MONDO:1012174)
megaesophagus, goat (MONDO:1012159)
arthrogryposis and palatoschisis syndrome, cattle (MONDO:1012015)
hypoadrenocorticism, dog (MONDO:1012109)
Dahlem dwarfism, rabbit (MONDO:1012496)
dysplasia epiphysealis hememelica, dog (MONDO:1012371)
hemolytic anemia, sheep (MONDO:1012097)
mammary tumor, dog (MONDO:1012448)
unilateral deafness and vestibular dysfunction, dog (MONDO:1012528)
selective ADP deficiency, dog (MONDO:1012453)
horn cancer, zebu cattle (MONDO:1012472)
sudden acquired retinal degeneration syndrome, dog (MONDO:1012523)
ocular squamous cell carcinoma, domestic cat (MONDO:1012195)
fibrodysplasia ossificans, domestic cat (MONDO:1012079)
dilute coat color with neurological defects, dog (MONDO:1012400)
chronic active hepatitis, dog (MONDO:1012290)
immunoglobulin 7S deficiency, chicken (MONDO:1012128)
tremor, cattle (MONDO:1012282)
facial eczema, cattle (MONDO:1012346)
intestinal cobalamin (vitamin B12) malabsorption, domestic cat (MONDO:1012452)
perosomus elumbis, horse (MONDO:1012208)
atrial septal defect and atrial fibrillation, horse (MONDO:1012019)
lower motor neuron disease, dog (MONDO:1012167)
vertebral and spinal dysplasia, cattle (MONDO:1012490)
tetragametic chimerism, dog (MONDO:1012083)
progressive ataxia with head tremor and seizures, dog (MONDO:1012372)
Guillain-Barr-like polyradiculoneuropathy, dog (MONDO:1012507)
dilute coat color with neurological defects, horse (MONDO:1012401)
congenital hypomyelinogenesis, sheep (MONDO:1012117)
forelimb-girdle muscular anomaly, cattle (MONDO:1012384)
congenital hydranencephaly and cerebellar hypoplasia, water buffalo (MONDO:1012434)
navicular disease, horse (MONDO:1012184)
caudal cruciate ligament disease, dog (MONDO:1012551)
hyperosmolar nonketotic diabetes mellitus, domestic cat (MONDO:1012062)
thrombasthenia, dog (MONDO:1012270)
spontaneous autoimmune thyroiditis, chicken (MONDO:1012021)
portosystemic hepatic encephalopathy, dog (MONDO:1012221)
retained placenta, horse (MONDO:1012552)
osteodystrophy, dog (MONDO:1012202)
cutaneous papillomatosis, horse (MONDO:1012306)
Enterococcus infectious disease (MONDO:1040019)
guttural pouch tympany, horse (MONDO:1012379)
retinal dystrophy, domestic cat (MONDO:1012243)
subclinical hypomagnesemia, cattle (MONDO:1012500)
faded shaker, chicken (MONDO:1012077)
exercise induced metabolic myopathy, dog (MONDO:1012517)
TRIP11-related skeletal dysplasia (MONDO:1040009)
quaking, golden hamster (MONDO:1012233)
lower motor neuron disease, horse (MONDO:1012168)
tomaculous neuropathy, cattle (MONDO:1012397)
neurological syndrome, horse (MONDO:1012192)
combined deficiency of factors IX and XII, domestic cat (MONDO:1012410)
rod dysplasia, dog (MONDO:1012431)
distal sensorimotor polyneuropathy, dog (MONDO:1012220)
retinal dystrophy, dog (MONDO:1012242)
micromelia, chicken (MONDO:1012164)
dystrophic epidermolysis bullosa, sheep (MONDO:1012072)
hydrallantois, sheep (MONDO:1012505)
rod-cone dysplasia, dog (MONDO:1012246)
megaesophagus, sheep (MONDO:1012160)
spondylosis deformans, dog (MONDO:1012301)
perinatal weak calf syndrome, cattle (MONDO:1012466)
Collie eye anomaly, dog (MONDO:1012051)
pituitary dwarfism, dog (MONDO:1012066)
cerebellar cortical atrophy, dog (MONDO:1012045)
multiple lipomatosis, dog (MONDO:1012141)
gastric dilatation volvulus syndrome, dog (MONDO:1012091)
chronic myelogenous leukemia, pig (MONDO:1012406)
spastic syndrome, cattle (MONDO:1012254)
tremor, chicken (MONDO:1012278)
granule cell type cerebellar hypoplasia, dog (MONDO:1012094)
atypical thrombasthenia, horse (MONDO:1012536)
androgen insensitivity syndrome, dog (MONDO:1012264)
perosomus elumbis, sheep (MONDO:1012211)
malignant hyperthermia, horse (MONDO:1012147)
intestinal cobalamin (vitamin B12) malabsorption, dog (MONDO:1012451)
dynamic laryngeal collapse, horse (MONDO:1012548)
focal metatarsal fistula, dog (MONDO:1012080)
immunoglobulin G deficiency, dog (MONDO:1012132)
intestinal fistula (MONDO:1040017)
anhidrotic ectodermal dysplasia EDAR-related, cattle (MONDO:1010792)
pectinate ligament dysplasia, dog (MONDO:1012515)
respiratory distress syndrome, pig (MONDO:1012025)
degenerative neuromuscular disease, cattle (MONDO:1012370)
hemophagocytic syndrome, domestic cat (MONDO:1012333)
spondylosis deformans, domestic cat (MONDO:1012302)
tetanic torticollar spasms, turkey (MONDO:1012269)
thrombasthenia, domestic cat (MONDO:1012271)
atypical myopathy, horse (MONDO:1012554)
progressive ataxia, dog (MONDO:1012287)
spastic syndrome, sheep (MONDO:1012255)
brachygnathia superior and degenerative joint disease, cattle (MONDO:1012034)
colorectal hamartomatous polyposis and ganglioneuromatosis, dog (MONDO:1012408)
tremor syndrome with central axonopathy, dog (MONDO:1012283)
primary seborrhea-oleosa, domestic cat (MONDO:1012222)
copper toxicosis, COMMD1-related, dog (MONDO:1010837)
infectious disease with sepsis (MONDO:1040015)
tremor, ducks (MONDO:1012277)
progressive myopathy, pig (MONDO:1012225)
Lundehund syndrome, dog (MONDO:1012497)
pseudocholinesterase deficiency, horse (MONDO:1012321)
spastic lameness, cattle (MONDO:1012250)
Text definitions added: 46

Most of these definitions are for new terms

Term New Text Definition
myelin oligodendrocyte glycoprotein antibody-associated disease (MONDO:1040024) A demyelinating disease of the central nervous system characterized by the presence of a demyelinating event (optic neuritis, myelitis, acute/multiphasic encephalomyelitis, cerebral or polyfocal deficits, brainstem or cerebellar deficits, and/or cerebral cortical encephalitis), a positive myelin oligodendrocyte glycorotein-IgG test, and exclusion of an alternative diagnosis like MS.
retinal degeneration, Smoky Joe, chicken (MONDO:1012474) Retinal degeneration that occurs in the Smoky Joe breed of chicken.
infectious disease with sepsis (MONDO:1040015) An infectious disease characterized by life-threatening organ dysfunction due to a dysreguated host response.
stomach ulcer, pig (MONDO:1012284) Stomach ulcer that occurs in pigs.
dyneinopathy (MONDO:1040031) A spectrum of diseases related to monoallelic variants in DYNC1H1 and characterized by variable neuromuscular and/or neurodevelopmental presentations. While not absolute, there appear to be genotype-phenotype correlations based on the location of the variant. Patients with variants in the stem domain of DYNC1H1 have been reported with a predominantly neuromuscular presentation, including congenital myopathy, spinal muscular atrophy, Charcot-Marie-Tooth (CMT), and less frequently, intellectual disability and autism. Patients with variants in the motor domain predominantly present with neurodevelopmental presentations including intellectual disability, seizures, malformations of cortical development (abnormal brain MRI findings such as pachygyria, heterotopias, enlarged ventricles, hypoplasia of CC, brain stem, cerebellum), autism, and less frequently, neuromuscular phenotypes.
megaesophagus, domestic ferret (MONDO:1012154) Megaesophagus that occurs in domestic ferret.
congenital stationary night blindness, TRPM1-related, horse (MONDO:1011255) Non-progressive vision impairment in dim or absent lighting in horses due to a variation in the TRPM1 gene. Specifically, horses homozygous for a white spotting phenotype, known as leopard complex spotting, are affected by CSNB.
Enterococcus infectious disease (MONDO:1040019) A bacterial disease caused by infection with Enterococcus.
cancer, domestic cat (MONDO:1012571) Cancer that occurs in domestic cats.
renal disease, dog (MONDO:1012235) Kidney disorder that occurs in dogs.
IRF6-related condition (MONDO:1040010) Van der Woude syndrome, popliteal pterygium syndrome, cleft lip with or without palate, or a spectrum of one or two of those conditions in which the cause of the disease is a mutation in the IRF6 gene.
EN1-related dorsoventral syndrome (MONDO:1040032) A human mesomelic and rhizo-mesomelic dysplasia characterized by marked mesomelic shortening of the lower limbs, cutaneous syndactyly and nail abnormalities (placed on the palmar side of the finger, dysplastic or absent) in hands and feet due mutations in EN1 gene. Other clinical features may include genitourinary abnormalities (including bilateral cryptorchidism, vesicoureteral reflux, hydronephrosis, hypoplastic labia majora), spasticity and seizures.
cerebral artery stenosis (MONDO:1040016) A cerebrovascular disorder characterized by an abnormal narrowing of a cerebral artery.
megaesophagus, dog (MONDO:1012153) Megaesophagus that occurs in dog.
Sharpin-related autoinflammatory syndrome (MONDO:1040029) An autoinflammatory disease in which the cause of the disease is a variation in the Sharpin gene.
copper toxicosis, COMMD1-related, dog (MONDO:1010837) Excess accumulation of copper in the liver with a centrilobular distribution in dogs due to a variation in the COMMD1 gene.
PIK3R2-related overgrowth spectrum (MONDO:1040004) Any overgrowth syndrome resulting from pathogenic gain-of-function variants in the PIK3R2 gene. The variants can be germline or somatic
congenital myasthenic syndrome, CHAT-related, dog (MONDO:1011029) An early onset syndrome of impaired neuromuscular transmission associated with a defect in acetylcholine synthesis in dogs due to a variation in the CHAT gene.
congenital stationary night blindness, LRIT3-related, dog (MONDO:1011262) Non-progressive vision impairment in dim or absent lighting in dogs due to a variation in the LRIT3 gene.
megaesophagus, horse (MONDO:1012156) Megaesophagus that occurs in horse.
postpartum amenorrhea-galactorrhea syndrome (MONDO:0043226) A postpartum condition consists of persistent lactation and amenorrhea in patients not breast feeding.
amelogenesis imperfecta, ENAM-related, dog (MONDO:1011202) An inherited disorder affecting the structure, composition, and quantity of tooth enamel in dogs due to a variation in the ENAM gene.
intestinal fistula (MONDO:1040017) An intestinal disorder characterized by an opening in the intestine to some epithelial surface.
GBA1-related Parkinson disease, susceptibility (MONDO:1040030) A susceptibility or predisposition to Parkinsons disease in which the cause of the disease is the presence of a monoallelic pathogenic variant or risk allele in the GBA1 gene.
cutaneous malignant melanoma in Sinclair swine, pig (MONDO:1012161) Cutaneous malignant melanoma that occurs in Sinclair swine.
cancer, pig (MONDO:1012572) Cancer that occurs in pigs.
megaesophagus, cattle (MONDO:1012158) Megaesophagus that occurs in cattle.
megaesophagus, domestic cat (MONDO:1012155) Megaesophagus that occurs in domestic cat.
congenital myasthenic syndrome, COLQ-related, dog (MONDO:1010932) An early onset syndrome of impaired neuromuscular transmission associated with an acetylcholinesterase deficiency in dogs due to a variation in the COLQ gene.
congenital myasthenic syndrome 4 (MONDO:1040021) Any postsynaptic congenital myasthenic syndrome in which the cause of the disease is a mutation in the CHRNE gene.
cancer, dog (MONDO:1012570) Cancer that occurs in dogs.
PI4KA-related disorder (MONDO:1040012) Any human disease in which the cause of the disease is a variation in the PI4KA gene. This disease is characterized primarily by neurologic dysfunction (limb spasticity, developmental delay, intellectual disability, seizures, ataxia, nystagmus), gastrointestinal manifestations (multiple intestinal atresia, inflammatory bowel disease), and combined immunodeficiency (leukopenia, variable immunoglobulin defects). Age of onset is typically antenatal or in early childhood; individuals can present with any combination of these features. Rare individuals present with later-onset hereditary spastic paraplegia. Brain MRI findings can include hypomyelinating leukodystrophy, cerebellar hypoplasia/atrophy, thin or dysplastic corpus callosum, and/or perisylvian polymicrogyria.
amelogenesis imperfecta, ACP4-related, dog (MONDO:1011209) An inherited disorder affecting the structure, composition, and quantity of tooth enamel in dogs due to a variation in the ACP4 gene.
MTOR-related overgrowth spectrum (MONDO:0100572) Any overgrowth syndrome in which the cause of the disease is a pathogenic gain-of-function variants in the MTOR gene. The variants can be germline or somatic.
methicillin-susceptible staphylococcus aureus infectious disease (MONDO:1040020) A bacterial infectious disease caused by methicillin-susceptible staphylococcus aureus.
megaesophagus, sheep (MONDO:1012160) Megaesophagus that occurs in sheep.
TRIP11-related skeletal dysplasia (MONDO:1040009) Any skeletal dysplasia in which the cause of the disease is a variation in the TRIP11 gene. Reduced protein function in TRIP11 causes a spectrum of skeletal symptoms from a more mild phenotype, called ondontochondrodysplasia, with features including short stature and joint laxity to a more severe phenotype, called achondrogenesis type 1A, which presents as a lethal prenatal or neonatal skeletal dysplasia. The clinical severity of achondrogenesis compared to ondontochondrodysplasia is related to the residual function of the gene which is not currently possible to anticipate based on genotype alone. The phenotype cannot fully be predicted by genotype alone, evidenced by variants being reported with both phenotypes.
vertebral artery dissection (MONDO:1040011) A human disorder which results from a tear in one of the major cervicocerebral arteries, allowing blood to enter the wall of the artery and split its layers. Pathogenesis typically leads to either stenosis or aneurysmal dilatation of the vessel.
developmental and epileptic encephalopathy, 31B (MONDO:0957248) Any developmental and epileptic encephalopathy in which the cause of the disease is a homozygous mutation in the DNM1 gene.
metastatic malignant neoplasm in the brain (MONDO:1040026) A malignant neoplasm that has spread to the brain from another anatomic site.
megaesophagus, llama (MONDO:1012157) Megaesophagus that occurs in llama.
congenital muscular dystrophy without intellectual disability (MONDO:1040033) A congenital muscular dystrophy due to dystroglycanopathy characterized by a wide phenotypic spectrum which includes hypotonia and muscular weakness present at birth or early infancy, delayed or arrested motor development, and normal intellectual abilities with normal (or only mild abnormalities) neuroimaging studies. Feeding difficulties, joint and spinal deformities, and respiratory insufficiency may be associated. Decreased alpha-dystroglycan on immunohistochemical muscle staining and elevated serum creatine kinase are observed.
anhidrotic ectodermal dysplasia EDAR-related, cattle (MONDO:1010792) An inherited syndrome characterized by hypotrichosis (sparseness of hair), hypo- or an-hidrosis (reduced ability to sweat), and hypodontia (congenital absence of teeth) in cattle due to a variation in the EDAR gene.
PIK3CA-related overgrowth spectrum (MONDO:1040002) Any overgrowth syndrome resulting from pathogenic gain-of-function variants in the PIK3CA gene. The variants can be germline or somatic
megaesophagus, goat (MONDO:1012159) Megaesophagus that occurs in goat.
Mollaret’s meningitis (MONDO:1030004) A rare clinical disorder characterized by at least three recurrent episodes of meningitis associated with spontaneous recovery with or without antiviral therapy. Herpes simplex virus type 2 has frequently been implicated in the setting of this illness. RBLM is rare with prevalence rates estimated at 2 per 100,000 persons.
Text definitions changed: 2
Term Old Text Definition New Text Definition
anal fistula (MONDO:0000754) A pathologic tract that connects an opening in the anal canal to the perianal skin. In the vast majority of cases there is a history of perianal abscess. An intestinal disorder characterized by an opening in the anal canal to the perianal skin. In the vast majority of cases there is a history of perianal abscess.
developmental and epileptic encephalopathy, 31A (MONDO:0014598) Any early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the DNM1 gene. Any developmental and epileptic encephalopathy in which the cause of the disease is a heterozygous mutation in the DNM1 gene.
Terms renamed (non-obsolete): 5
ID Old Label New Label
MONDO:1011934 laryngeal collapse, dynamic, non-human animal dynamic laryngeal collapse, non-human animal
MONDO:0032717 amelogenesis imperfecta, type 3c amelogenesis imperfecta, type 3C
MONDO:0014598 developmental and epileptic encephalopathy, 31 developmental and epileptic encephalopathy, 31A
MONDO:1011928 laryngeal paralysis, generic, non-human animal laryngeal paralysis, non-human animal
MONDO:0957248 developmental and epileptic encephalopathy 31B developmental and epileptic encephalopathy, 31B
Terms obsoleted with replacement: 1
Term Replacement
obsolete choroideremia-hypopituitarism syndrome (MONDO:0015429) choroideremia hypopituitarism (MONDO:0022737)
Relationships added: 2600

New: "curated content resource" linkout to ClinGen pages (only 10 shown here)

| Subject | Predicate | Object| ----|----|----| | neurodevelopmental disorder with cerebellar atrophy and with or without seizures (MONDO:0020841) | curated content resource (curated_content_resource) | https://search.clinicalgenome.org/kb/conditions/MONDO:0020841 | | Ehlers-Danlos syndrome, classic type, 1 (MONDO:0019567) | curated content resource (curated_content_resource) | https://search.clinicalgenome.org/kb/conditions/MONDO:0019567 | | focal segmental glomerulosclerosis 4, susceptibility to (MONDO:0012931) | curated content resource (curated_content_resource) | https://search.clinicalgenome.org/kb/conditions/MONDO:0012931 | | ciliary dyskinesia, primary, 37 (MONDO:0033204) | curated content resource (curated_content_resource) | https://search.clinicalgenome.org/kb/conditions/MONDO:0033204 | | tetragametic chimerism, pig (MONDO:1012084) | subClassOf (rdfs:subClassOf) | tetragametic chimerism, non-human animal (MONDO:1011918) | | SIN3A-related intellectual disability syndrome (MONDO:0044699) | curated content resource (curated_content_resource) | https://search.clinicalgenome.org/kb/conditions/MONDO:0044699 | | hypochondroplasia (MONDO:0007793) | curated content resource (curated_content_resource) | https://search.clinicalgenome.org/kb/conditions/MONDO:0007793 | | Bruton-type agammaglobulinemia (MONDO:0010421) | curated content resource (curated_content_resource) | https://search.clinicalgenome.org/kb/conditions/MONDO:0010421 | | ALG6-congenital disorder of glycosylation 1C (MONDO:0011291) | curated content resource (curated_content_resource) | https://search.clinicalgenome.org/kb/conditions/MONDO:0011291 | | STAT3-related early-onset multisystem autoimmune disease (MONDO:0014414) | curated content resource (curated_content_resource) | https://search.clinicalgenome.org/kb/conditions/MONDO:0014414 |
Mappings added: 3589 (only 10 shown here)

Many new mappings to icd11.foundation
Many mappings to OMIA (non-human animal diseases)

Subject Predicate Object
relapsing-remitting multiple sclerosis (MONDO:0005314) oio:hasDbXref icd11.foundation:799053936
tremor, domestic cat (MONDO:1012280) oio:hasDbXref OMIA:001016-9685
tertiary hyperparathyroidism (MONDO:0021132) oio:hasDbXref icd11.foundation:10683191
multiple lipomatosis, pig (MONDO:1012142) oio:hasDbXref OMIA:000606-9823
tetragametic chimerism, cattle (MONDO:1012085) oio:hasDbXref OMIA:000393-9913
benign neoplasm of gallbladder (MONDO:0021503) oio:hasDbXref icd11.foundation:1439916526
cor pulmonale (MONDO:0004596) oio:hasDbXref icd11.foundation:738218522
frostbite (MONDO:0800177) oio:hasDbXref icd11.foundation:152692065
bilateral deafness and vestibular dysfunction, pig (MONDO:1012521) oio:hasDbXref OMIA:002148-9823
breast implant-associated anaplastic large cell lymphoma (MONDO:0850112) oio:hasDbXref Orphanet:667662
Mappings removed (non obsolete terms):
Subject Predicate Object
hepatic porphyria (MONDO:0002520) oio:hasDbXref Orphanet:95157
craniofacial microsomia (MONDO:0015397) oio:hasDbXref NORD:1518
galactorrhea (MONDO:0009256) oio:hasDbXref OMIM:230300
Hurler-Scheie syndrome (MONDO:0011759) oio:hasDbXref SCTID:73123008
metachromatic leukodystrophy, juvenile form (MONDO:0009591) oio:hasDbXref SCTID:238031009

Other changes

  • The following ontology variants have been removed from the release: mondo-with-equivalents ; mondo-minimal.