ZFIN Human Disease: spermatogenic failure 56

OBO ID: DOID:0112336

Term Name:	spermatogenic failure 56		Search Ontology:
Synonyms:	SPGF56
Definition:	A spermatogenic failure characterized by male infertility due to multiple morphologic abnormalities of the flagella with severely reduced sperm motility that has_material_basis_in homozygous or compound heterozygous mutation in the DNAH10 gene on chromosome 12q24.31. https://pubmed.ncbi.nlm.nih.gov/34237282/
References:	OMIM:619515
Ontology:	Human Disease ( DOID:0112336 )

Relationships

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

OTHER spermatogenic failure 56 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
DNAH10	dnah10	Spermatogenic failure 56	619515

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None