Disease #01870 (Iminoglycinuria, OMIM:242600)

Official abbreviation -
Name Iminoglycinuria
OMIM ID 242600
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 3 genes SLC36A2, SLC6A19, SLC6A20
Associated tissues -
Disease features -
Remarks -