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764961009: Hereditary primary clear cell renal cell carcinoma (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5180538019 Hereditary primary clear cell renal cell carcinoma (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5180539010 Hereditary primary clear cell renal cell carcinoma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5180540012 Hereditary primary clear cell renal cell adenocarcinoma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5404432014 Hereditary clear cell renal cell carcinoma (ccRCC) is a hereditary renal cancer syndrome defined as development of ccRCC in two or more family members without evidence of constitutional chromosome 3 translocation, von Hippel-Lindau disease or other tumor predisposing syndromes associated with ccRCC, such as tuberous sclerosis or Birt-Hogg-Dubé syndrome. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5404433016 Hereditary clear cell renal cell carcinoma (ccRCC) is a hereditary renal cancer syndrome defined as development of ccRCC in two or more family members without evidence of constitutional chromosome 3 translocation, von Hippel-Lindau disease or other tumour predisposing syndromes associated with ccRCC, such as tuberous sclerosis or Birt-Hogg-Dubé syndrome. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3655784011 Hereditary clear cell renal cell carcinoma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3655785012 Hereditary clear cell renal cell adenocarcinoma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3655787016 Hereditary clear cell renal cell carcinoma (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5180538019 Hereditary primary clear cell renal cell carcinoma (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5180539010 Hereditary primary clear cell renal cell carcinoma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5180540012 Hereditary primary clear cell renal cell adenocarcinoma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3657276012 A hereditary renal cancer syndrome defined as development of hereditary clear cell renal cell carcinoma (ccRCC) in two or more family members without evidence of constitutional chromosome 3 translocation, von Hippel-Lindau disease or other neoplasm predisposing syndromes associated with ccRCC, such as tuberous sclerosis or Birt-Hogg-Dubbe syndrome. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5404432014 Hereditary clear cell renal cell carcinoma (ccRCC) is a hereditary renal cancer syndrome defined as development of ccRCC in two or more family members without evidence of constitutional chromosome 3 translocation, von Hippel-Lindau disease or other tumor predisposing syndromes associated with ccRCC, such as tuberous sclerosis or Birt-Hogg-Dubé syndrome. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5404433016 Hereditary clear cell renal cell carcinoma (ccRCC) is a hereditary renal cancer syndrome defined as development of ccRCC in two or more family members without evidence of constitutional chromosome 3 translocation, von Hippel-Lindau disease or other tumour predisposing syndromes associated with ccRCC, such as tuberous sclerosis or Birt-Hogg-Dubé syndrome. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3437181001000114 Nierenzellkarzinom, klarzelliges, hereditäre Form de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
918351000172117 carcinome rénal héréditaire à cellules claires fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
918531000172118 adénocarcinome rénal héréditaire à cellules claires fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
918351000172117 carcinome rénal héréditaire à cellules claires fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
918531000172118 adénocarcinome rénal héréditaire à cellules claires fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3437181001000114 Nierenzellkarzinom, klarzelliges, hereditäre Form de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary primary clear cell renal cell carcinoma (disorder) Is a Familial neoplastic disease false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary primary clear cell renal cell carcinoma (disorder) Is a Clear cell carcinoma of kidney false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary primary clear cell renal cell carcinoma (disorder) Is a Hereditary cancer-predisposing syndrome false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary primary clear cell renal cell carcinoma (disorder) Is a Hereditary nephropathy (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary primary clear cell renal cell carcinoma (disorder) Associated morphology Clear cell adenocarcinoma false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary primary clear cell renal cell carcinoma (disorder) Finding site Structure of parenchyma of kidney true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary primary clear cell renal cell carcinoma (disorder) Is a Familial renal cell carcinoma (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary primary clear cell renal cell carcinoma (disorder) Associated morphology Clear cell renal cell carcinoma true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary primary clear cell renal cell carcinoma (disorder) Is a Primary clear cell carcinoma of kidney (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary primary clear cell renal cell carcinoma (disorder) Pathological process (attribute) Malignant proliferation of primary neoplasm (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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