Disease #03145 (CGL3 (lipodystrophy, congenital generalized, type 3), OMIM:612526)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	CGL3
Name	lipodystrophy, congenital generalized, type 3
OMIM ID	612526
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	CAV1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2024-06-28 14:53:44 +02:00 (CEST)

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