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Mondo Disease Ontology
MONDO
All terms in MONDO
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Label
Id
Description
intrauterine growth restriction-congenital multiple café-au-lait macules-increased sister chromatid exchange syndrome
MONDO_0034991
intellectual disability-cardiac anomalies-short stature-joint laxity syndrome
MONDO_0034989
coloboma of eyelid
MONDO_0020357
Al Kaissi syndrome
MONDO_0044324
coloboma of iris
MONDO_0020356
Rahman syndrome
MONDO_0044323
coloboma of eye lens
MONDO_0020355
granular corneal dystrophy type I
MONDO_0007377
developmental delay and seizures with or without movement abnormalities
MONDO_0044326
posterior polymorphous corneal dystrophy 1
MONDO_0007378
coloboma of choroid and retina
MONDO_0020354
Fanconi anemia, complementation group W
MONDO_0044325
von Hippel anomaly
MONDO_0020353
Peters anomaly
MONDO_0011414
epithelial basement membrane dystrophy
MONDO_0007375
retinitis pigmentosa 79
MONDO_0044320
fleck corneal dystrophy
MONDO_0007376
multiple system atrophy, parkinsonian type
MONDO_0020352
Blake pouch cyst
MONDO_0020351
corneal degeneration, ribbonlike, with deafness
MONDO_0007373