ZFIN Human Disease: spermatogenic failure 65

OBO ID: DOID:0112354

Term Name:	spermatogenic failure 65		Search Ontology:
Synonyms:	SPGF65
Definition:	A spermatogenic failure characterized by male infertility due to asthenoteratozoospermia with severely reduced or absent progressive sperm motillity and multiple morphologic abnormalities of the flagella that has_material_basis_in homozygous or compound heterozygous mutation in the DHND1 gene on chromosome 11p15.4. https://pubmed.ncbi.nlm.nih.gov/34932939/
References:	OMIM:619712
Ontology:	Human Disease ( DOID:0112354 )

Relationships

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

OTHER spermatogenic failure 65 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
DNHD1	dnhd1	Spermatogenic failure 65	619712

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None