OBO ID: DOID:0111387
Term Name: familial isolated hypoparathyroidism Search Ontology:
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 familial isolated hypoparathyroidism PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
PTH Hypoparathyroidism, familial isolated 1 146200
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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