ZFIN Human Disease: spermatogenic failure 23

OBO ID: DOID:0070181

Term Name:	spermatogenic failure 23		Search Ontology:
Synonyms:	SPGF23
Definition:	A spermatogenic failure that is characterized by autosomal recessive inhertitance of nonobstructive azoospermia that has_material_basis_in mutation in the TEX14 gene on chromosome 17q23. https://www.ncbi.nlm.nih.gov/pubmed/28206990
References:	OMIM:617707
Ontology:	Human Disease ( DOID:0070181 )

Relationships

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

OTHER spermatogenic failure 23 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
TEX14	tex14	Spermatogenic failure 23	617707

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None