Search Ontology:
Human Disease

familial isolated hypoparathyroidism

Term ID
DOID:0111387
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. (2)
References
Ontology
Human Disease   ( DOID:0111387 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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