|OBO ID: DOID:0111923|
|Term Name:||spermatogenic failure 42||Search Ontology:|
|Definition:||A spermatogenic failure characterized by multiple morphologic abnormalities of the flagella resulting in severly impaired sperm progressive motility and infertility that has_material_basis_in homozygous or compound heterozygous mutation in TTC29 on chromosome 4q31.22. (2)|
|Ontology:||Human Disease (DOID:0111923)|
|is a type of:||
OTHER spermatogenic failure 42 PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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