FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term Y-linked spermatogenic failure 1 ID (Ontology) DOID:0070186 (Human Disease)
Definition A Sertoli cell-only syndrome that has_material_basis_in deletions in the Yq11 chromosomal region.
Also Known As "SPGFY1" ; "type I Sertoli cell-only syndrome" ; "Y-linked Sertoli cell-only syndrome"
Comment
Links to External Ontologies
DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
No relevant records available
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: 
monogenic disease
 |__Y-linked monogenic disease_____
chromosomal disease                |
 |__chromosomal deletion syndrome__|
male infertility                   |
 |__Sertoli cell-only syndrome_____|
                                   Y-linked spermatogenic failure 1
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a Sertoli cell-only syndrome
Y-linked monogenic disease
chromosomal deletion syndrome
Part of
hide Synonyms & Secondary IDs
Synonyms
  • "SPGFY1" EXACT OMO:0003012
    "type I Sertoli cell-only syndrome" EXACT
    "Y-linked Sertoli cell-only syndrome" EXACT
Secondary IDs
hide External Crossreferences & Linkouts
MIM:400042