ZFIN Human Disease: spermatogenic failure 43

OBO ID: DOID:0111917

Term Name:	spermatogenic failure 43		Search Ontology:
Synonyms:	SPGF43
Definition:	A spermatogenic failure characterized by multiple morphologic abnormalities of the flagella resulting in absence of forward motility in spermatozoa and infertility that has_material_basis_in homozygous or compound heterozygous mutation in the SPEF2 gene on chromosome 5p13.2. (2)
References:	OMIM:618751
Ontology:	Human Disease ( DOID:0111917 )

Relationships

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

OTHER spermatogenic failure 43 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
SPEF2	spef2	Spermatogenic failure 43	618751

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None