Disease #04357 (FHBL2 (hypobetalipoproteinemia, familial, type 2 (FHBL2)), OMIM:605019)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	FHBL2
Name	hypobetalipoproteinemia, familial, type 2 (FHBL2)
OMIM ID	605019
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	ANGPTL3
Associated tissues	-
Disease features	-
Remarks	-
Date created	2015-09-23 10:25:22 +02:00 (CEST)
Date last edited	2020-02-26 12:55:05 +01:00 (CET)

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