ZFIN Human Disease: spermatogenic failure 19

OBO ID: DOID:0070170

Term Name:	spermatogenic failure 19		Search Ontology:
Synonyms:	SPGF19
Definition:	A spermatogenic failure that is characterized by autosomal recessive inheritance of sperm flagellar morphological abnormalities that has_material_basis_in mutation in the CFAP43 gene on chromosome 10q25. https://www.ncbi.nlm.nih.gov/pubmed/28552195
References:	OMIM:617592
Ontology:	Human Disease ( DOID:0070170 )

Relationships

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

OTHER spermatogenic failure 19 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
CFAP43	cfap43	Spermatogenic failure 19	617592

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None