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 )

Relationships
is a type of: hypoparathyroidism