FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term autosomal dominant hypocalcemia ID (Ontology) DOID:0090109 (Human Disease)
Definition A metal metabolism disorder characterized by autosomal dominant inheritance of variable degrees of hypocalcemia with normal to low levels of parathyroid hormone.
Also Known As "HYPOC"
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
No relevant statements available
Spanning Tree (Parents/Children)
Only view relationship: 
autosomal genetic disease
 |__autosomal dominant disease__
inherited metabolic disorder    |
 |__metal metabolism disorder___|
                                autosomal dominant hypocalcemia  1 rec.
                                 |__autosomal dominant hypocalcemia 1
                                 |__autosomal dominant hypocalcemia 2 1 rec.
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a autosomal dominant disease
metal metabolism disorder
Part of
hide Synonyms & Secondary IDs
Synonyms
  • "HYPOC" EXACT OMO:0003012
Secondary IDs
hide External Crossreferences & Linkouts
GARD:2877
ICD10CM:E20.8
MIM:PS601198
ORDO:428