About   Help   FAQ
Disease Ontology Browser
familial hypocalciuric hypercalcemia 2 (DOID:0060701)
Alliance: disease page
Synonyms: familial hypocalciuric hypercalcemia type 2; FHH type 2; HHC2; hypocalciuric hypercalcemia type II
Alt IDs: OMIM:145981, ICD10CM:E83.5, ORDO:101049
Definition: A familial hypocalciuric hypercalcemia that has_material_basis_in heterozygous mutation in the GNA11 gene on chromosome 19p13.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
MGI 6.12
The Jackson Laboratory