MONDO_merge Find_IDs Find_Terms Annotation
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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
prefrontal, with bone cysts dementia C536329
multiple epiphyseal dysplasia with robin phenotype C563291
progressive, with lipomembranous polycystic osteodysplasia dementia C536329
epiphyseal dysplasia, multiple, with robin phenotype C563291
Asthesioneuroblastoma (morphologic abnormality) 6329
Esthesioneuroepithelioma (morphologic abnormality) 6329
esthesioneuroblastoma (morphologic abnormality) 6329
retinitis pigmentosa, and sutural cataract microcephaly C563296
congenital, blue dot type, 2 cataract C563294
paranasal sinus olfactory neuroblastoma 6329
multiple, with robin phenotype epiphyseal dysplasia C563291
syndrome associated with hypertrophic cardiomyopathy http://purl.obolibrary.org/obo/MONDO_0016329