Disease #01350 (hyperglycinuria (hyperglycinuria), OMIM:138500)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	hyperglycinuria
Name	hyperglycinuria
OMIM ID	138500
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 3 genes	SLC36A2, SLC6A19, SLC6A20
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2020-02-09 13:41:52 +01:00 (CET)

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