Search Ontology:
Human Disease

familial hypocalciuric hypercalcemia 2

Term ID
DOID:0060701
Synonyms
  • familial hypocalciuric hypercalcemia type 2
  • FHH type 2
  • HHC2
  • hypocalciuric hypercalcemia type II
Definition
A familial hypocalciuric hypercalcemia that has_material_basis_in heterozygous mutation in the GNA11 gene on chromosome 19p13. https://www.ncbi.nlm.nih.gov/pubmed/23802516
References
Ontology
Human Disease   ( DOID:0060701 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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