About: Lynch syndrome

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

OMIM mapping confirmed by DO. [SN].

Attributes	Values
type	Class
subClassOf	autosomal dominant disease syndrome nodeID://b50952421
label	Lynch syndrome
comment	OMIM mapping confirmed by DO. [SN].
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:3883
has_alternative_id	DOID:0050586 DOID:3040
database_cross_reference	GARD:9905 MESH:D003123 NCI:C120083 OMIM:PS120435 ORDO:144 SNOMEDCT_US_2021_09_01:315058005 UMLS_CUI:C0009405 UMLS_CUI:C1333990
has_exact_synonym	COCA 1 (en) HNPCC - hereditary nonpolyposis colon cancer (en) Hereditary Defective Mismatch Repair syndrome (en) hereditary nonpolyposis colorectal cancer (en) hereditary nonpolyposis colorectal neoplasm (en)
has_obo_namespace	disease_ontology
in_subset	DO_rare_slim NCIthesaurus
http://purl.obolib...g/obo/IAO_0000115	A syndrome that is characterized by an increased risk for colon cancer and cancers of the endometrium, ovary, stomach, small intestine, hepatobiliary tract, urinary tract, brain, and skin and has_material_basis_in mutation of mismatch repair genes that increases the risk of many types of cancers.
is subClassOf of	Muir-Torre syndrome hereditary nonpolyposis colorectal cancer type 8 Lynch syndrome 1 hereditary nonpolyposis colorectal cancer type 5 hereditary nonpolyposis colorectal cancer type 6 hereditary nonpolyposis colorectal cancer type 2 hereditary nonpolyposis colorectal cancer type 4 hereditary nonpolyposis colorectal cancer type 7
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50952422

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