Disease #01833 (HPABH4B (hyperphenylalaninemia, BH4-deficient, type B), OMIM:233910)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	HPABH4B
Name	hyperphenylalaninemia, BH4-deficient, type B
OMIM ID	233910
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	GCH1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2022-11-07 08:59:38 +01:00 (CET)

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