FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term renal hypomagnesemia 6 ID (Ontology) DOID:0060884 (Human Disease)
Definition A hypomagnesemia characterized by autosomal dominant inheritance of severely lowered serum magnesium levels without other electrolyte disturbances or abnormalities in urinary magnesium excretion that has_material_basis_in heterozygous mutation in the CNNM2 gene on chromosome 10q24.
Also Known As "HOMG6"
Comment
Links to External Ontologies
DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
    Results list data from multiple species. Click on a button above and use the 'Filter by species' options on the resulting HitList to retrieve species-specific data.
Records annotated with this exact term (annotations to child terms are NOT included)
No relevant records available
show Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
 Full annotation statements 
Relevant FlyBase reports
 Genes
 renal hypomagnesemia 6       1
 for disease ribbon | renal hypomagnesemia 6       1
 model of | renal hypomagnesemia 6       1
Spanning Tree (Parents/Children)
Only view relationship: 
  metal metabolism disorder
   |__primary hypomagnesemia
       |__renal hypomagnesemia 6  1 rec.
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a primary hypomagnesemia
Part of
hide Synonyms & Secondary IDs
Synonyms
  • "HOMG6" EXACT OMO:0003012
Secondary IDs
hide External Crossreferences & Linkouts
GARD:12155
ICD10CM:E83.4
MIM:613882
ORDO:34527