OBO ID: DOID:0060701
Term Name: familial hypocalciuric hypercalcemia 2 Search Ontology:
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 familial hypocalciuric hypercalcemia 2 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
GNA11 Hypocalciuric hypercalcemia, type II 145981
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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