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Metadata
ID	DOID:0070588
Name	spermatogenic failure 89
Definition	A spermatogenic failure characterized by severely reduced progressive motility of sperm that has_material_basis_in homozygous or compound heterozygous mutation in the AK9 gene on chromosome 6q21. https://pubmed.ncbi.nlm.nih.gov/37713809/
Xrefs	MIM:620705
SKOS	exactMatch MIM:620705
Synonyms	SPGF89 [EXACT]
Parent Relationships	is_a spermatogenic failure is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance