ZFIN Human Disease: spermatogenic failure 41

OBO ID: DOID:0111912

Term Name:	spermatogenic failure 41		Search Ontology:
Synonyms:	SPGF41
Definition:	A spermatogenic failure characterized by oligozoospermia and multiple morphologic abnormalities of the flagella that has_material_basis_in homozygous or compound heterozygous mutation in the CFAP70 gene on chromosome 10q22.2. https://pubmed.ncbi.nlm.nih.gov/31621862/
References:	OMIM:618670
Ontology:	Human Disease ( DOID:0111912 )

Relationships

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

OTHER spermatogenic failure 41 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
CFAP70	cfap70	?Spermatogenic failure 41	618670

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None