|OBO ID: DOID:0111919|
|Term Name:||spermatogenic failure 38||Search Ontology:|
|Definition:||A spermatogenic failure characterized by multiple morphologic abnormalities of the flagella resulting in infertility and asthenoteratozoospermia that has_material_basis_in homozygous or compound heterozygous mutation in ARMC2 on chromosome 6q21. https://pubmed.ncbi.nlm.nih.gov/30686508/|
|Ontology:||Human Disease (DOID:0111919)|
|is a type of:||
OTHER spermatogenic failure 38 PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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