Term Name: spermatogenic failure 32
Synonyms: SPGF32
Definition: A spermatogenic failure characterized by nonobstructive azoospermia, absence of spermatogenic cells and a Sertoli cell-only phenotype in testes that has_material_basis_in heterozygous mutation in the SOHLH1 gene on chromosome 9q34.3.
Ontology: Human Disease [DOID:0111925]   ( DOID:0111925 )

Relationships
is a type of: autosomal dominant disease spermatogenic failure