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
pignata guarino syndrome C536781
CACH VWM syndrome D056784
central nervous system toxoplasmosis D016781
long qt syndrome 12 C567842
lymphedema of the lower extremities, recurrent pneumonia, bronchiectasis, and yellowed nails C538678
malaria, plasmodium vivax D016780
hepatic vein thrombosis 6786
crossed polydactyly, type i C566783
x-linked, snyder-robinson type mental retardation C536678
epithelioid trophoblastic tumor 16787
autosomal recessive, type IIB cutis laxa C567855
familial keratoconus with cataract 13678
keratoconus, familial, with early-onset anterior polar cataract 13678
hyperinsulinism, infantile, with enteropathy and deafness 11678
generalized epilepsy with febrile seizures plus, 7 C567827