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DO Term : Lynch syndrome 1 [DOID:0070271] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A Lynch syndrome that has_material_basis_in heterozygous mutations in the MSH2 gene on chromosome 2p21-p16.

synonyms:
hereditary nonpolyposis colorectal cancer type 1,
UMLS_CUI:C2936783,
HNPCC1,
120435,
NCI:C6725,
OMIM:120435,
familial nonpolyposis colon cancer type 1,
COCA1,
FCC1

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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