About: Werner syndrome

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

OMIM mapping confirmed by DO. [LS].

Attributes	Values
type	Class
subClassOf	autosomal recessive disease syndrome nodeID://b50954267
label	Werner syndrome
comment	OMIM mapping confirmed by DO. [LS].
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:5688
database_cross_reference	GARD:7885 MESH:D014898 NCI:C3447 OMIM:277700 ORDO:902 SNOMEDCT_US_2021_09_01:51626007 UMLS_CUI:C0043119
has_exact_synonym	WS (en) Werner's syndrome (en) adult premature ageing syndrome (en) adult progeria (en)
has_obo_namespace	disease_ontology
in_subset	DO_FlyBase_slim DO_rare_slim NCIthesaurus
http://purl.obolib...g/obo/IAO_0000115	A syndrome characterized by premature aging and age-related phenotypes such as atherosclerosis, arteriosclerosis, cataracts, osteoporosis, soft tissue calcification, premature thinning, graying, and loss of hair, as well as a high incidence of some types of cancers and that has_material_basis_in mutations in the WRN gene, on chromosome 8.
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50954268

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