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

Official abbreviation hyperglycinuria
Name hyperglycinuria
OMIM ID 138500
Human Phenotype Ontology Project (HPO) HPO
Inheritance AD
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 3 genes SLC36A2, SLC6A19, SLC6A20
Associated tissues -
Disease features -
Remarks -