|OBO ID: DOID:0111912|
|Term Name:||spermatogenic failure 41||Search Ontology:|
|Definition:||A spermatogenic failure characterized by oligozoospermia and multiple morphologic abnormalities of the flagella that has_material_basis_in homozygous or compound heterozygous mutation in CFAP70 on chromosome 10q22.2. https://pubmed.ncbi.nlm.nih.gov/31621862/|
|Ontology:||Human Disease (DOID:0111912)|
|is a type of:||
OTHER spermatogenic failure 41 PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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