|OBO ID: DOID:0112337|
|Term Name:||spermatogenic failure 55||Search Ontology:|
|Definition:||A spermatogenic failure characterized by male infertility due to asthenozoospermia, with severely reduced sperm motility that has_material_basis_in homozygous or compound heterozygous mutation in SPAG17 on chromosome 1p12. https://pubmed.ncbi.nlm.nih.gov/28548327/|
|Ontology:||Human Disease (DOID:0112337)|
|is a type of:||
OTHER spermatogenic failure 55 PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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