Disease #01426 (HOMG-2 (hypomagnesemia, type 2, renal (HOMG-2)), OMIM:154020)

Official abbreviation HOMG-2
Name hypomagnesemia, type 2, renal (HOMG-2)
OMIM ID 154020
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene FXYD2
Associated tissues -
Disease features -
Remarks -