Disease #02009 (HPABH4A (hyperphenylalaninemia, BH4-deficient, type A), OMIM:261640)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
Register as submitter | Log in

Official abbreviation	HPABH4A
Name	hyperphenylalaninemia, BH4-deficient, type A
OMIM ID	261640
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	PTS
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2022-11-07 08:59:08 +01:00 (CET)

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.