Disease #01996 (HP-2 (hyperoxaluria, primary, type II (HP-2)), OMIM:260000)

Official abbreviation HP-2
Name hyperoxaluria, primary, type II (HP-2)
OMIM ID 260000
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene GRHPR
Associated tissues -
Disease features -
Remarks -