Search Ontology:
Human Disease

spermatogenic failure 19

Term ID
DOID:0070170
Synonyms
  • SPGF19
Definition
A spermatogenic failure that is characterized by autosomal recessive inheritance of sperm flagellar morphological abnormalities that has_material_basis_in mutation in the CFAP43 gene on chromosome 10q25. https://www.ncbi.nlm.nih.gov/pubmed/28552195
References
Ontology
Human Disease   ( DOID:0070170 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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