ZFIN Human Disease: spermatogenic failure 22

OBO ID: DOID:0070177

Term Name:	spermatogenic failure 22		Search Ontology:
Synonyms:	SPGF22
Definition:	A spermatogenic failure that is characterized by autosomal recessive inheritance of spermatocyte maturation arrest resulting in azoospermia that has_material_basis_in mutation in the MEIOB gene on chromosome 16p13. https://www.ncbi.nlm.nih.gov/pubmed/28206990
References:	OMIM:617706
Ontology:	Human Disease ( DOID:0070177 )

Relationships

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

OTHER spermatogenic failure 22 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
MEIOB	meiob	Spermatogenic failure 22	617706

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None