About: spermatogenic failure 51

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An Entity of Type : owl:Class, within Data Space : linkeddata.uriburner.com:28898 associated with source document(s)

Attributes	Values
type	Class
subClassOf	autosomal recessive disease spermatogenic failure nodeID://b50946416
label	spermatogenic failure 51
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:0112273
database_cross_reference	OMIM:619177
has_exact_synonym	SPGF51
has_obo_namespace	disease_ontology
http://purl.obolib...g/obo/IAO_0000115	A spermatogenic failure characterized by severe asthenoteratozoospermia with multiple morphologic abnormalities of the flagella resulting in reduced to absent motility that has_material_basis_in homozygous or compound heterozygous mutation in CFAP91 on chromosome 3q13.33.
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50946417

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