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Metadata
ID	DOID:0111925
Name	spermatogenic failure 32
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. https://pubmed.ncbi.nlm.nih.gov/20506135/
Xrefs	MIM:618115
Synonyms	SPGF32 [EXACT]
Parent Relationships	is_a autosomal dominant disease is_a spermatogenic failure
Subclass Logical Relationships	has material basis in some autosomal dominant inheritance