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Human Disease

spermatogenic failure 38

Term ID
DOID:0111919
Synonyms
  • 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 )
Relationships
is a type of
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Genes Involved
Zebrafish Models