|OBO ID: DOID:0070170|
|Term Name:||spermatogenic failure 19||Search Ontology:|
|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|
|Ontology:||Human Disease (DOID:0070170)|
|is a type of:||
OTHER spermatogenic failure 19 PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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