ZFIN Human Disease: spermatogenic failure 33

OBO ID: DOID:0111915

Term Name:	spermatogenic failure 33		Search Ontology:
Synonyms:	SPGF33
Definition:	A spermatogenic failure characterized by multiple morphologic abnormalities of the flagella resulting in immotile spermatozoa and infertility that has_material_basis_in homozygous or compound heterozygous mutation in the WDR66 gene on chromosome 12q24.31. https://pubmed.ncbi.nlm.nih.gov/30122540/
References:	OMIM:618152
Ontology:	Human Disease ( DOID:0111915 )

Relationships

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

OTHER spermatogenic failure 33 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
WDR66	cfap251	Spermatogenic failure 33	618152

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None