Search Ontology:
Human Disease
spermatogenic failure 37
- Term ID
- DOID:0111927
- Synonyms
-
- SPGF37
- Definition
- A spermatogenic failure characterized by multiple morphologic abnormalities of the flagella, asthenoteratozoospermia, and infertility that has_material_basis_in homozygous or compound heterozygous mutation in the TTC21A gene on chromosome 3p22.2. https://pubmed.ncbi.nlm.nih.gov/30929735/
- References
- Ontology
- Human Disease ( DOID:0111927 )
- is a type of
-
Other Pages
Genes Involved
Zebrafish Models