ZFIN Human Disease: spermatogenic failure 5

OBO ID: DOID:0070183

Term Name:	spermatogenic failure 5		Search Ontology:
Synonyms:	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:	GARD:12385 MESH:C562903 OMIM:243060 ORDO:137893 SNOMEDCT_US_2021_09_01:236806004
Ontology:	Human Disease ( DOID:0070183 )

Relationships

is a type of:	autosomal recessive disease spermatogenic failure autosomal recessive disease spermatogenic failure Show first 5 Terms

OTHER spermatogenic failure 5 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
AURKC		Spermatogenic failure 5

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None