FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term hypogonadotropic hypogonadism 24 without anosmia ID (Ontology) DOID:0090088 (Human Disease)
Definition A hypogonadotropic hypogonadism that has_material_basis_in homozygous or compound heterozygous mutation in the FSHB gene on chromosome 11p14.
Also Known As "isolated follicle-stimulating hormone deficiency"
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
 hypogonadotropic hypogonadism 24 without anosmia       1
 for disease ribbon | hypogonadotropic hypogonadism 24 without anosmia       1
 model of | hypogonadotropic hypogonadism 24 without anosmia       1
Spanning Tree (Parents/Children)
Only view relationship: 
autosomal genetic disease
 |__autosomal recessive disease____
hypogonadism                       |
 |__hypogonadotropic hypogonadism__|
                                   hypogonadotropic hypogonadism 24 without anosmia  1 rec.
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a autosomal recessive disease
hypogonadotropic hypogonadism
Part of
hide Synonyms & Secondary IDs
Synonyms
  • "isolated follicle-stimulating hormone deficiency" EXACT
Secondary IDs
hide External Crossreferences & Linkouts
ICD10CM:E23.6
MIM:229070
ORDO:52901