1197359006: Familial colorectal cancer type X (disorder)

SNOMED CT Concept\Clinical finding\...

\Viscus structure finding\Abdominal organ finding\...

\Bowel finding\Finding of large intestine\Observation of colon\Mass of colon\Neoplasm of colon\Malignant neoplasm of colon\Primary malignant neoplasm of colon\Hereditary nonpolyposis colon cancer\Familial colorectal cancer type X
\Bowel finding\Finding of large intestine\Observation of colon\Disorder of colon\Colonic lesion\Neoplasm of colon\Malignant neoplasm of colon\Primary malignant neoplasm of colon\Hereditary nonpolyposis colon cancer\Familial colorectal cancer type X
\Bowel finding\Finding of large intestine\Disorder of large intestine\Disorder of colon\Colonic lesion\Neoplasm of colon\Malignant neoplasm of colon\Primary malignant neoplasm of colon\Hereditary nonpolyposis colon cancer\Familial colorectal cancer type X
\Bowel finding\Finding of large intestine\Disorder of large intestine\Neoplasm of large intestine\Malignant neoplasm of large intestine\Malignant neoplasm of colon and/or rectum\Malignant neoplasm of colon\Primary malignant neoplasm of colon\Hereditary nonpolyposis colon cancer\Familial colorectal cancer type X
\Bowel finding\Finding of large intestine\Disorder of large intestine\Neoplasm of large intestine\Malignant neoplasm of large intestine\Primary malignant neoplasm of large intestine\Primary malignant neoplasm of colon\Hereditary nonpolyposis colon cancer\Familial colorectal cancer type X
\Bowel finding\Finding of large intestine\Disorder of large intestine\Neoplasm of large intestine\Neoplasm of colon\Malignant neoplasm of colon\Primary malignant neoplasm of colon\Hereditary nonpolyposis colon cancer\Familial colorectal cancer type X
\Bowel finding\Intestinal disease\Neoplasm of intestinal tract\Malignant tumour of intestine\Primary malignant neoplasm of intestinal tract\Primary malignant neoplasm of large intestine\Primary malignant neoplasm of colon\Hereditary nonpolyposis colon cancer\Familial colorectal cancer type X
\Bowel finding\Intestinal disease\Neoplasm of intestinal tract\Malignant tumour of intestine\Malignant neoplasm of large intestine\Malignant neoplasm of colon and/or rectum\Malignant neoplasm of colon\Primary malignant neoplasm of colon\Hereditary nonpolyposis colon cancer\Familial colorectal cancer type X
\Bowel finding\Intestinal disease\Neoplasm of intestinal tract\Malignant tumour of intestine\Malignant neoplasm of large intestine\Primary malignant neoplasm of large intestine\Primary malignant neoplasm of colon\Hereditary nonpolyposis colon cancer\Familial colorectal cancer type X
\Bowel finding\Intestinal disease\Neoplasm of intestinal tract\Neoplasm of large intestine\Malignant neoplasm of large intestine\Malignant neoplasm of colon and/or rectum\Malignant neoplasm of colon\Primary malignant neoplasm of colon\Hereditary nonpolyposis colon cancer\Familial colorectal cancer type X
\Bowel finding\Intestinal disease\Neoplasm of intestinal tract\Neoplasm of large intestine\Malignant neoplasm of large intestine\Primary malignant neoplasm of large intestine\Primary malignant neoplasm of colon\Hereditary nonpolyposis colon cancer\Familial colorectal cancer type X
\Bowel finding\Intestinal disease\Neoplasm of intestinal tract\Neoplasm of large intestine\Neoplasm of colon\Malignant neoplasm of colon\Primary malignant neoplasm of colon\Hereditary nonpolyposis colon cancer\Familial colorectal cancer type X
\Bowel finding\Intestinal disease\Disorder of large intestine\Disorder of colon\Colonic lesion\Neoplasm of colon\Malignant neoplasm of colon\Primary malignant neoplasm of colon\Hereditary nonpolyposis colon cancer\Familial colorectal cancer type X
\Bowel finding\Intestinal disease\Disorder of large intestine\Neoplasm of large intestine\Malignant neoplasm of large intestine\Malignant neoplasm of colon and/or rectum\Malignant neoplasm of colon\Primary malignant neoplasm of colon\Hereditary nonpolyposis colon cancer\Familial colorectal cancer type X
\Bowel finding\Intestinal disease\Disorder of large intestine\Neoplasm of large intestine\Malignant neoplasm of large intestine\Primary malignant neoplasm of large intestine\Primary malignant neoplasm of colon\Hereditary nonpolyposis colon cancer\Familial colorectal cancer type X
\Bowel finding\Intestinal disease\Disorder of large intestine\Neoplasm of large intestine\Neoplasm of colon\Malignant neoplasm of colon\Primary malignant neoplasm of colon\Hereditary nonpolyposis colon cancer\Familial colorectal cancer type X

Status: current, Primitive. 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 Initial character case insensitive SNOMED CT core

4695999017 Familial colorectal cancer type X en Synonym Active Initial character case insensitive SNOMED CT core

4696000015 FCCTX - familial colorectal cancer type X en Synonym Active Case sensitive 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 Case sensitive 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 Case sensitive SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Familial colorectal cancer type X	Is a	Hereditary nonpolyposis colon cancer	true	Inferred relationship	Some
Familial colorectal cancer type X	Finding site	Colon structure	true	Inferred relationship	Some	1
Familial colorectal cancer type X	Associated morphology	Neoplasm, malignant (primary)	false	Inferred relationship	Some	1
Familial colorectal cancer type X	Associated morphology	Malignant neoplasm	true	Inferred relationship	Some	1
Familial colorectal cancer type X	Pathological process	Primary malignant neoplastic proliferation	true	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Clinical finding foundation reference set

Neoplasm and/or hamartoma reference set

Problem/Diagnosis reference set

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Id	Description	Lang	Type	Status	Case?	Module
4695998013	Familial colorectal cancer type X (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
4695999017	Familial colorectal cancer type X	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
4696000015	FCCTX - familial colorectal cancer type X	en	Synonym	Active	Case sensitive	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	Case sensitive	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	Case sensitive	SNOMED CT core