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Metadata
ID	DOID:0111923
Name	spermatogenic failure 42
Definition	A spermatogenic failure characterized by multiple morphologic abnormalities of the flagella resulting in severly impaired sperm progressive motility and infertility that has_material_basis_in homozygous or compound heterozygous mutation in the TTC29 gene on chromosome 4q31.22. https://pubmed.ncbi.nlm.nih.gov/31735292/, https://pubmed.ncbi.nlm.nih.gov/31735294/
Xrefs	MIM:618745
Synonyms	SPGF42 [EXACT]
Parent Relationships	is_a spermatogenic failure is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance