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Human Disease
spermatogenic failure 42
- Term ID
- DOID:0111923
- Synonyms
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- SPGF42
- 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. (2)
- References
- Ontology
- Human Disease ( DOID:0111923 )
- is a type of
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