ZFIN Human Disease: spermatogenic failure 40

OBO ID: DOID:0111918

Term Name:	spermatogenic failure 40		Search Ontology:
Synonyms:	SPGF40
Definition:	A spermatogenic failure characterized by multiple morphologic abnormalities of the flagella resulting in severely reduced to absent sperm motility and abnormalities of the sperm head that has_material_basis_in homozygous or compound heterozygous mutation in the CFAP65 gene on chromosome 2q35. https://pubmed.ncbi.nlm.nih.gov/31413122/
References:	OMIM:618664
Ontology:	Human Disease ( DOID:0111918 )

Relationships

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

OTHER spermatogenic failure 40 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
CFAP65	cfap65	Spermatogenic failure 40	618664

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None