Search Ontology:
Human Disease

spermatogenic failure 92

Term ID
DOID:0070591
Synonyms
  • SPGF92
Definition
A spermatogenic failure characterized by asthenozoospermia that has_material_basis_in homozygous mutation in the LRRC23 gene on chromosome 12p13.31. (2)
References
Ontology
Human Disease   ( DOID:0070591 )
Relationships
is a type of
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Genes Involved
Zebrafish Models