Disease #02769 (CGL1 (lipodystrophy, generalized, congenital, type 1 (CGL-1)), OMIM:608594)

Official abbreviation CGL1
Name lipodystrophy, generalized, congenital, type 1 (CGL-1)
OMIM ID 608594
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 1
Associated with 1 gene AGPAT2
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00204201 - - - F yes Iran - - - - - CGL1 Berardinelli Seip syndrome and FSGS AGPAT2 AGPAT2 1 1 Aida Rasoolzadeh
00240355 - - - - - - - - - - - CGL1 - AGPAT2 AGPAT2 1 1 Nilay Gunes
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