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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
FPLD4 13478
PLIN1-related FPLD 13478
childhood ependymoma 3478
pediatric ependymoma 3478
ependymoma of childhood 3478
cast syndrome D013478
syndrome, cast D013478
syndrome, wilkie D013478
wilkie syndrome D013478
rhizomelic, with callosal agenesis, thrombocytopenia, hydrocephalus, and hypertension osteochondrodysplasia C563478
PLIN1-related familial partial lipodystrophy 13478
mesenteric duodenal compression syndrome D013478
familial partial lipodystrophy associated with PLIN1 mutations 13478
familial partial lipodystrophy type 4 13478
lipodystrophy, familial partial, associated with Plin1 mutations 13478