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

There is 0 pattern entry.

Label
Id
FPLD4 13478
PLIN1-related FPLD 13478
familial partial lipodystrophy associated with PLIN1 mutations 13478
cast syndrome D013478
syndrome, cast D013478
syndrome, wilkie D013478
wilkie syndrome D013478
mesenteric duodenal compression syndrome D013478
familial partial lipodystrophy type 4 13478
duodenal compression syndrome, mesenteric D013478
PLIN1-related familial partial lipodystrophy 13478
lipodystrophy, familial partial, associated with Plin1 mutations 13478
lipodystrophy, familial partial, type 4 13478
lipodystrophy, familial partial, type 4; FPLD4 http://purl.obolibrary.org/obo/MONDO_0013478
FPLD due to PLIN1 mutations 13478
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