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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 )
Relationships
is a type of
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Genes Involved
Zebrafish Models
Citations