Search Ontology:
Human Disease
spermatogenic failure 38
- Term ID
- DOID:0111919
- Synonyms
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- SPGF38
- 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 the ARMC2 gene on chromosome 6q21. https://pubmed.ncbi.nlm.nih.gov/30686508/
- References
- Ontology
- Human Disease ( DOID:0111919 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models