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
BSCL1 12071
CGL1 12071
Brunzell syndrome, Agpat2-Related http://purl.obolibrary.org/obo/MONDO_0012071
Brunzell syndrome, Agpat2-related 12071
lipodystrophy, Berardinelli-Seip congenital, type 1 12071
AGPAT2 congenital generalized lipodystrophy (disease) 12071
lipodystrophy, congenital generalized, type 1 12071
lipodystrophy, congenital generalized, type 1; CGL1 http://purl.obolibrary.org/obo/MONDO_0012071
congenital generalized lipodystrophy (disease) caused by mutation in AGPAT2 12071
Berardinelli-Seip congenital lipodystrophy type 1 12071
congenital generalized lipodystrophy type 1 12071
Berardinelli-Seip congenital lipodystrophy, type 1 12071
AGPAT2-related Brunzell syndrome 12071