ZFIN Human Disease: spermatogenic failure 55

OBO ID: DOID:0112337

Term Name:	spermatogenic failure 55		Search Ontology:
Synonyms:	SPGF55
Definition:	A spermatogenic failure characterized by male infertility due to asthenozoospermia, with severely reduced sperm motility that has_material_basis_in homozygous or compound heterozygous mutation in the SPAG17 gene on chromosome 1p12. https://pubmed.ncbi.nlm.nih.gov/28548327/
References:	OMIM:619380
Ontology:	Human Disease ( DOID:0112337 )

Relationships

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

OTHER spermatogenic failure 55 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
SPAG17	spag17	?Spermatogenic failure 55	619380

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None