Search Ontology:
Human Disease

spermatogenic failure 21

Term ID
DOID:0070163
Synonyms
Definition
A male infertility due to acephalic spermatozoa that is characterized by acephalic spermatozoa, reduced sperm number and impaired sperm motility that has_material_basis_in homozygous mutation in the BRDT gene on chromosome 1p22. https://www.ncbi.nlm.nih.gov/pubmed/28199965
References
Ontology
Human Disease   ( DOID:0070163 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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