ZFIN Human Disease: spermatogenic failure 13

OBO ID: DOID:0070182

Term Name:	spermatogenic failure 13		Search Ontology:
Synonyms:	SPGF13
Definition:	A spermatogenic failure that is characterized by autosomal recessive inheritance of azoospermia or oligozoospermia that has_material_basis_in mutation in the TAF4B gene on chromosome 18q11. https://www.ncbi.nlm.nih.gov/pubmed/24431330
References:	OMIM:615841
Ontology:	Human Disease ( DOID:0070182 )

Relationships

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

OTHER spermatogenic failure 13 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
TAF4B	taf4b	?Spermatogenic failure 13	615841

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None