| Disease Aliases (19) | Agpat2 congenital generalized lipodystrophy (disease) Agpat2-related brunzell syndrome Berardinelli-seip congenital lipodystrophy, type 1 Brunzell syndrome, agpat2-related Bscl1 Berardinelli-seip congenital lipodystrophy type 1 Berardinelli-seip congenital lipodystrophy Brunzell syndrome agpat2-related Cgl1 Congenital generalized lipodystrophy type 1 Lipodystrophy, berardinelli-seip congenital, type 1 Agpat2-related Berardinelli-seip congenital Brunzell syndrome Congenital generalized lipodystrophy (disease) caused by mutation in agpat2 Lipodystrophy, congenital generalized, type 1 Lipodystrophy, congenital generalized, type 1; cgl1 |
Associated Genes (1) NCBI-RefSeq: AGPAT2 (1-acylglycerol-3-phosphate O-acyltransferase 2) External Links: gnomAD browser Ensembl GeneCards
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| Cross-references of Congenital generalized lipodystrophy type 1 | OMIM | GARD | Orphanet | NCBI-GTR | NCBI-MedGen | MalaCards | MeSH | Annotations | |