ZFIN Human Disease: spermatogenic failure 42

OBO ID: DOID:0111923

Term Name:	spermatogenic failure 42		Search Ontology:
Synonyms:	SPGF42
Definition:	A spermatogenic failure characterized by multiple morphologic abnormalities of the flagella resulting in severly impaired sperm progressive motility and infertility that has_material_basis_in homozygous or compound heterozygous mutation in the TTC29 gene on chromosome 4q31.22. (2)
References:	OMIM:618745
Ontology:	Human Disease ( DOID:0111923 )

Relationships

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

OTHER spermatogenic failure 42 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
TTC29	ttc29	Spermatogenic failure 42	618745

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None