Disease #02783 (APLD (lipodystrophy, partial, acquired, susceptibility to), OMIM:608709)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	APLD
Name	lipodystrophy, partial, acquired, susceptibility to
OMIM ID	608709
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	LMNB2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2025-04-17 19:23:41 +02:00 (CEST)

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