1197359006: Familial colorectal cancer type X (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Viscus structure finding (finding)\Abdominal organ finding\...

\Bowel finding\Finding of large intestine\Observation of colon (finding)\Mass of colon (finding)\Neoplasm of colon\Malignant tumour of colon\Primary malignant neoplasm of colon\HNPCC - hereditary nonpolyposis colon cancer\Familial colorectal cancer type X (disorder)
\Bowel finding\Finding of large intestine\Observation of colon (finding)\Disorder of colon (disorder)\Colonic lesion\Neoplasm of colon\Malignant tumour of colon\Primary malignant neoplasm of colon\HNPCC - hereditary nonpolyposis colon cancer\Familial colorectal cancer type X (disorder)
\Bowel finding\Finding of large intestine\Disorder of large intestine\Disorder of colon (disorder)\Colonic lesion\Neoplasm of colon\Malignant tumour of colon\Primary malignant neoplasm of colon\HNPCC - hereditary nonpolyposis colon cancer\Familial colorectal cancer type X (disorder)
\Bowel finding\Finding of large intestine\Disorder of large intestine\Neoplasm of large intestine\Malignant tumour of large intestine\Colorectal cancer\Malignant tumour of colon\Primary malignant neoplasm of colon\HNPCC - hereditary nonpolyposis colon cancer\Familial colorectal cancer type X (disorder)
\Bowel finding\Finding of large intestine\Disorder of large intestine\Neoplasm of large intestine\Malignant tumour of large intestine\Primary malignant neoplasm of large intestine\Primary malignant neoplasm of colon\HNPCC - hereditary nonpolyposis colon cancer\Familial colorectal cancer type X (disorder)
\Bowel finding\Finding of large intestine\Disorder of large intestine\Neoplasm of large intestine\Neoplasm of colon\Malignant tumour of colon\Primary malignant neoplasm of colon\HNPCC - hereditary nonpolyposis colon cancer\Familial colorectal cancer type X (disorder)
\Bowel finding\Disorder of intestine\Neoplasm of intestinal tract\Malignant tumour of intestine\Primary malignant neoplasm of intestinal tract (disorder)\Primary malignant neoplasm of large intestine\Primary malignant neoplasm of colon\HNPCC - hereditary nonpolyposis colon cancer\Familial colorectal cancer type X (disorder)
\Bowel finding\Disorder of intestine\Neoplasm of intestinal tract\Malignant tumour of intestine\Malignant tumour of large intestine\Colorectal cancer\Malignant tumour of colon\Primary malignant neoplasm of colon\HNPCC - hereditary nonpolyposis colon cancer\Familial colorectal cancer type X (disorder)
\Bowel finding\Disorder of intestine\Neoplasm of intestinal tract\Malignant tumour of intestine\Malignant tumour of large intestine\Primary malignant neoplasm of large intestine\Primary malignant neoplasm of colon\HNPCC - hereditary nonpolyposis colon cancer\Familial colorectal cancer type X (disorder)
\Bowel finding\Disorder of intestine\Neoplasm of intestinal tract\Neoplasm of large intestine\Malignant tumour of large intestine\Colorectal cancer\Malignant tumour of colon\Primary malignant neoplasm of colon\HNPCC - hereditary nonpolyposis colon cancer\Familial colorectal cancer type X (disorder)
\Bowel finding\Disorder of intestine\Neoplasm of intestinal tract\Neoplasm of large intestine\Malignant tumour of large intestine\Primary malignant neoplasm of large intestine\Primary malignant neoplasm of colon\HNPCC - hereditary nonpolyposis colon cancer\Familial colorectal cancer type X (disorder)
\Bowel finding\Disorder of intestine\Neoplasm of intestinal tract\Neoplasm of large intestine\Neoplasm of colon\Malignant tumour of colon\Primary malignant neoplasm of colon\HNPCC - hereditary nonpolyposis colon cancer\Familial colorectal cancer type X (disorder)
\Bowel finding\Disorder of intestine\Disorder of large intestine\Disorder of colon (disorder)\Colonic lesion\Neoplasm of colon\Malignant tumour of colon\Primary malignant neoplasm of colon\HNPCC - hereditary nonpolyposis colon cancer\Familial colorectal cancer type X (disorder)
\Bowel finding\Disorder of intestine\Disorder of large intestine\Neoplasm of large intestine\Malignant tumour of large intestine\Colorectal cancer\Malignant tumour of colon\Primary malignant neoplasm of colon\HNPCC - hereditary nonpolyposis colon cancer\Familial colorectal cancer type X (disorder)
\Bowel finding\Disorder of intestine\Disorder of large intestine\Neoplasm of large intestine\Malignant tumour of large intestine\Primary malignant neoplasm of large intestine\Primary malignant neoplasm of colon\HNPCC - hereditary nonpolyposis colon cancer\Familial colorectal cancer type X (disorder)
\Bowel finding\Disorder of intestine\Disorder of large intestine\Neoplasm of large intestine\Neoplasm of colon\Malignant tumour of colon\Primary malignant neoplasm of colon\HNPCC - hereditary nonpolyposis colon cancer\Familial colorectal cancer type X (disorder)

\Neoplasm of intra-abdominal organs\Malignant neoplasm of intraabdominal organ (disorder)\Malignant tumour of intestine\Primary malignant neoplasm of intestinal tract (disorder)\Primary malignant neoplasm of large intestine\Primary malignant neoplasm of colon\HNPCC - hereditary nonpolyposis colon cancer\Familial colorectal cancer type X (disorder)
\Neoplasm of intra-abdominal organs\Malignant neoplasm of intraabdominal organ (disorder)\Malignant tumour of intestine\Malignant tumour of large intestine\Colorectal cancer\Malignant tumour of colon\Primary malignant neoplasm of colon\HNPCC - hereditary nonpolyposis colon cancer\Familial colorectal cancer type X (disorder)
\Neoplasm of intra-abdominal organs\Malignant neoplasm of intraabdominal organ (disorder)\Malignant tumour of intestine\Malignant tumour of large intestine\Primary malignant neoplasm of large intestine\Primary malignant neoplasm of colon\HNPCC - hereditary nonpolyposis colon cancer\Familial colorectal cancer type X (disorder)
\Neoplasm of intra-abdominal organs\Malignant neoplasm of intraabdominal organ (disorder)\Primary malignant neoplasm of intra-abdominal organs\Primary malignant neoplasm of intestinal tract (disorder)\Primary malignant neoplasm of large intestine\Primary malignant neoplasm of colon\HNPCC - hereditary nonpolyposis colon cancer\Familial colorectal cancer type X (disorder)
\Neoplasm of intra-abdominal organs\Neoplasm of intestinal tract\Malignant tumour of intestine\Primary malignant neoplasm of intestinal tract (disorder)\Primary malignant neoplasm of large intestine\Primary malignant neoplasm of colon\HNPCC - hereditary nonpolyposis colon cancer\Familial colorectal cancer type X (disorder)
\Neoplasm of intra-abdominal organs\Neoplasm of intestinal tract\Malignant tumour of intestine\Malignant tumour of large intestine\Colorectal cancer\Malignant tumour of colon\Primary malignant neoplasm of colon\HNPCC - hereditary nonpolyposis colon cancer\Familial colorectal cancer type X (disorder)
\Neoplasm of intra-abdominal organs\Neoplasm of intestinal tract\Malignant tumour of intestine\Malignant tumour of large intestine\Primary malignant neoplasm of large intestine\Primary malignant neoplasm of colon\HNPCC - hereditary nonpolyposis colon cancer\Familial colorectal cancer type X (disorder)
\Neoplasm of intra-abdominal organs\Neoplasm of intestinal tract\Neoplasm of large intestine\Malignant tumour of large intestine\Colorectal cancer\Malignant tumour of colon\Primary malignant neoplasm of colon\HNPCC - hereditary nonpolyposis colon cancer\Familial colorectal cancer type X (disorder)
\Neoplasm of intra-abdominal organs\Neoplasm of intestinal tract\Neoplasm of large intestine\Malignant tumour of large intestine\Primary malignant neoplasm of large intestine\Primary malignant neoplasm of colon\HNPCC - hereditary nonpolyposis colon cancer\Familial colorectal cancer type X (disorder)
\Neoplasm of intra-abdominal organs\Neoplasm of intestinal tract\Neoplasm of large intestine\Neoplasm of colon\Malignant tumour of colon\Primary malignant neoplasm of colon\HNPCC - hereditary nonpolyposis colon cancer\Familial colorectal cancer type X (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 28-Feb 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

4695998013 Familial colorectal cancer type X (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

4695999017 Familial colorectal cancer type X en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

4696000015 FCCTX - familial colorectal cancer type X en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

4695996012 A rare hereditary nonpolyposis colon cancer defined in individuals meeting the Amsterdam criteria for Lynch syndrome, but lacking germline mutations in the mismatch repair genes. It is characterised by a later onset, preferential involvement of distal colon and rectum, lower risk of developing extracolonic cancer, a higher adenoma/carcinoma ratio, a higher differentiation of tumour cells, a more heterogeneous tumour architecture and an infiltrative growth pattern when compared to Lynch syndrome cases. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

4695997015 A rare hereditary nonpolyposis colon cancer defined in individuals meeting the Amsterdam criteria for Lynch syndrome, but lacking germline mutations in the mismatch repair genes. It is characterized by a later onset, preferential involvement of distal colon and rectum, lower risk of developing extracolonic cancer, a higher adenoma/carcinoma ratio, a higher differentiation of tumor cells, a more heterogeneous tumor architecture and an infiltrative growth pattern when compared to Lynch syndrome cases. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

5630841000052110 familjär kolorektal cancer, typ X sv Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Familial colorectal cancer type X (disorder)	Is a	HNPCC - hereditary nonpolyposis colon cancer	true	Inferred relationship	Some
Familial colorectal cancer type X (disorder)	Finding site	Colon structure	true	Inferred relationship	Some	1
Familial colorectal cancer type X (disorder)	Associated morphology	tumör, malign (primär)	false	Inferred relationship	Some	1
Familial colorectal cancer type X (disorder)	Associated morphology	Malignant neoplasm (morphologic abnormality)	true	Inferred relationship	Some	1
Familial colorectal cancer type X (disorder)	Pathological process (attribute)	Malignant proliferation of primary neoplasm (qualifier value)	true	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
4695998013	Familial colorectal cancer type X (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
4695999017	Familial colorectal cancer type X	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
4696000015	FCCTX - familial colorectal cancer type X	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
4695996012	A rare hereditary nonpolyposis colon cancer defined in individuals meeting the Amsterdam criteria for Lynch syndrome, but lacking germline mutations in the mismatch repair genes. It is characterised by a later onset, preferential involvement of distal colon and rectum, lower risk of developing extracolonic cancer, a higher adenoma/carcinoma ratio, a higher differentiation of tumour cells, a more heterogeneous tumour architecture and an infiltrative growth pattern when compared to Lynch syndrome cases.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
4695997015	A rare hereditary nonpolyposis colon cancer defined in individuals meeting the Amsterdam criteria for Lynch syndrome, but lacking germline mutations in the mismatch repair genes. It is characterized by a later onset, preferential involvement of distal colon and rectum, lower risk of developing extracolonic cancer, a higher adenoma/carcinoma ratio, a higher differentiation of tumor cells, a more heterogeneous tumor architecture and an infiltrative growth pattern when compared to Lynch syndrome cases.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5630841000052110	familjär kolorektal cancer, typ X	sv	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Sweden NRC maintained module (core metadata concept)