About: spermatogenic failure 12

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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 dominant disease spermatogenic failure nodeID://b50939842
label	spermatogenic failure 12
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:0070171
database_cross_reference	OMIM:615413
has_exact_synonym	SPGF12 (en)
has_obo_namespace	disease_ontology
http://purl.obolib...g/obo/IAO_0000115	A male infertility characterized by autosomal dominant inheritance of azoospermia or severe oligoasthenoteratozoospermia and in some cases a Sertolic cell-only phenotype that has_material_basis_in heterozygous mutation in the NANOS1 gene on chromosome 10q26.
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50939843

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