Search Ontology:
Human Disease
spermatogenic failure 5
- Term ID
- DOID:0070183
- Synonyms
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- Infertility associated with multi-tailed spermatozoa and excessive deoxyribonucleic acid
- infertility associated with multitailed spermatozoa and excessive DNA
- macrocephalic sperm head syndrome
- male infertility due to macrozoospermia
- male infertility with large-headed, multiflagellar, polyploid spermatozoa
- SPGF5
- Definition
- A spermatogenic failure that is characterized by autosomal recessive inheritance of large-headed, multiflagellar, polyploid spermatozoa that has_material_basis_in mutation in the AURKC gene on chromosome 19q13. https://www.ncbi.nlm.nih.gov/pubmed/17435757
- References
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- GARD:12385
- MESH:C562903
- MIM:243060
- ORDO:137893
- SNOMEDCT_US_2021_09_01:236806004
- Ontology
- Human Disease ( DOID:0070183 )
- is a type of
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Genes Involved
Zebrafish Models