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Metadata
ID	DOID:0111926
Name	spermatogenic failure 39
Definition	A spermatogenic failure characterized by multiple morphologic anomalies of the sperm flagellum, lack of the outer dynein arms in the flagella, and asthenozoospermia that has_material_basis_in homozygous or compound heterozygous mutation in the DNAH17 gene on chromosome 17q25.3. https://pubmed.ncbi.nlm.nih.gov/31178125/
Xrefs	MIM:618643
Synonyms	SPGF39 [EXACT]
Parent Relationships	is_a spermatogenic failure is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance