MONDO_merge Find_IDs Find_Terms Annotation
manager
language -
license -
created at 2021-12-22 03:08:20 UTC
updated at 2021-12-22 07:06:09 UTC
MONDO_bioport_pref_name
183,974 entries
Label
Id
retinitis pigmentosa, and sutural cataract microcephaly C563296
cataract, congenital, blue dot type, 2 C563294
prefrontal, with bone cysts dementia C536329
congenital, blue dot type, 2 cataract C563294
epiphyseal dysplasia, multiple, with robin phenotype C563291
progressive, with lipomembranous polycystic osteodysplasia dementia C536329
multiple epiphyseal dysplasia with robin phenotype C563291
multiple, with robin phenotype epiphyseal dysplasia C563291
paranasal sinus olfactory neuroblastoma 6329
syndrome associated with hypertrophic cardiomyopathy http://purl.obolibrary.org/obo/MONDO_0016329
congenital, cerulean type, 2 cataract C563294
ectopia lentis, spontaneous filtering blebs, and craniofacial dysmorphism C563293