ZFIN Human Disease: spermatogenic failure 38

OBO ID: DOID:0111919

Term Name:	spermatogenic failure 38		Search Ontology:
Synonyms:	SPGF38
Definition:	A spermatogenic failure characterized by multiple morphologic abnormalities of the flagella resulting in infertility and asthenoteratozoospermia that has_material_basis_in homozygous or compound heterozygous mutation in the ARMC2 gene on chromosome 6q21. https://pubmed.ncbi.nlm.nih.gov/30686508/
References:	OMIM:618433
Ontology:	Human Disease ( DOID:0111919 )

Relationships

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

OTHER spermatogenic failure 38 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
ARMC2	armc2	Spermatogenic failure 38	618433

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None