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Human Disease

spermatogenic failure 42

Term ID
DOID:0111923
Synonyms
  • 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 )
Relationships
is a type of
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Genes Involved
Zebrafish Models