ZFIN Human Disease: spermatogenic failure 59

OBO ID: DOID:0112357

Term Name:	spermatogenic failure 59		Search Ontology:
Synonyms:	SPGF59
Definition:	A spermatogenic failure that is characterized by male infertility due to nonobstructive azoospermia that has_material_basis_in homozygous or compound heterozygous mutation in the TERB2 gene on chromosome 15q21.1. https://pubmed.ncbi.nlm.nih.gov/33211200/
References:	OMIM:619645
Ontology:	Human Disease ( DOID:0112357 )

Relationships

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

OTHER spermatogenic failure 59 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
TERB2	terb2	?Spermatogenic failure 59	619645

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None