Phenotype #0000154686

Global Variome shared LOVD

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

	Curator: Global Variome, with Curator vacancy

Individual ID	00180961
Associated disease	HPANBH4
Diagnosis/Initial	hyperphenylalaninemia
Diagnosis/Definite	HPANBH4
Phenotype details	hyperphenylalaninemia (HP:0004923)
Inheritance	Familial, autosomal recessive
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Belen Perez
Database submission license
Created by	Johan den Dunnen
Date created	2018-11-16 15:25:30 +01:00 (CET)
Date last edited	N/A

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