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DO Term : familial hypocalciuric hypercalcemia 2 [DOID:0060701] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A familial hypocalciuric hypercalcemia that has_material_basis_in heterozygous mutation in the GNA11 gene on chromosome 19p13.
  • synonyms:
  • OMIM:145981,
  • 145981,
  • ORDO:101049,
  • HHC2,
  • GARD:9758,
  • hypocalciuric hypercalcemia type II,
  • ICD10CM:E83.5,
  • FHH type 2,
  • familial hypocalciuric hypercalcemia type 2
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents





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