|OBO ID: DOID:0111914|
|Term Name:||spermatogenic failure 35||Search Ontology:|
|Definition:||A spermatogenic failure characterized by multiple morphologic abnormalities of the flagella resulting in severely impaired sperm motility and infertility that has_material_basis_in homozygous or compound heterozygous mutation in QRICH2 on chromosome 17q25.1. https://pubmed.ncbi.nlm.nih.gov/30683861/|
|Ontology:||Human Disease (DOID:0111914)|
|is a type of:||
OTHER spermatogenic failure 35 PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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