Search Ontology:
Human Disease
autosomal dominant hypocalcemia 2
- Term ID
- DOID:0090108
- Synonyms
-
- HYPOC2
- Definition
- An autosomal dominant hypocalcemia that has_material_basis_in heterozygous mutation in the G protein subunit alpha 11 gene (GNA11) on chromosome 19p13. (2)
- References
- Ontology
- Human Disease ( DOID:0090108 )
- is a type of
-
Show first 5 Terms
Other Pages
Genes Involved
Zebrafish Models
Citations