Term Name:	familial isolated hypoparathyroidism
Synonyms:	FIH
Definition:	A hypoparathyroidism that has_material_basis_in mutation in PTH on chromosome 6p24.2 or in the GCM2 gene on chromosome 11p15.3.
Ontology:	Human Disease [DOID:0111387]   ( DOID:0111387 )