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Human Disease

spermatogenic failure 35

Term ID
DOID:0111914
Synonyms
  • SPGF35
Definition
A spermatogenic failure characterized by multiple morphologic abnormalities of the flagella resulting in severely impaired sperm motility and infertility that has_material_basis_in homozygous or compound heterozygous mutation in the QRICH2 gene on chromosome 17q25.1. https://pubmed.ncbi.nlm.nih.gov/30683861/
References
Ontology
Human Disease   ( DOID:0111914 )
Relationships
is a type of
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Genes Involved
Zebrafish Models