Disease #00892

Official abbreviation FIH
Name hypoparathyroidism, familial isolated (FIH)
OMIM ID 146200
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 2 genes GCM2, PTH
Associated tissues -
Disease features autosomal dominant
Remarks -