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302849000: Nephroblastoma (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
444810016 Nephroblastoma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
444812012 Nephroma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
699012017 Nephroblastoma (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2988937013 Wilm's tumor en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3037411011 Wilms tumour en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3037540011 Wilms tumor en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
1851421000195117 nefroblastoma it Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
112141000172116 tumeur de Wilms fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
348711000172117 néphroblastome fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
906131000195117 Wilms-Tumor de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3420251001000110 Nephroblastom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

6 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Nephroblastoma Is a Malignant neoplasm of kidney parenchyma true Inferred relationship Some
Nephroblastoma Finding site Kidney structure false Inferred relationship Some 1
Nephroblastoma Associated morphology Nephroblastoma false Inferred relationship Some 1
Nephroblastoma Pathological process Malignant neoplastic process false Inferred relationship Some
Nephroblastoma Is a Primary malignant neoplasm of kidney false Inferred relationship Some
Nephroblastoma Finding site Structure of parenchyma of kidney false Inferred relationship Some 1
Nephroblastoma Is a Primary malignant neoplasm of retroperitoneum (disorder) false Inferred relationship Some
Nephroblastoma Finding site Kidney structure false Inferred relationship Some 1
Nephroblastoma Associated morphology néoplasie maligne (morphologie) false Inferred relationship Some 2
Nephroblastoma Is a Primary malignant neoplasm of retroperitoneum (disorder) false Inferred relationship Some
Nephroblastoma Associated morphology Nephroblastoma true Inferred relationship Some 1
Nephroblastoma Finding site Structure of parenchyma of kidney true Inferred relationship Some 1
Nephroblastoma Is a Hereditary disorder of the urinary system false Inferred relationship Some
Nephroblastoma Is a Hereditary cancer-predisposing syndrome false Inferred relationship Some
Nephroblastoma Is a Hereditary nephropathy (disorder) false Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
11p partial monosomy syndrome Is a False Nephroblastoma Inferred relationship Some
History of nephroblastoma (situation) Associated finding False Nephroblastoma Inferred relationship Some 1
History of nephroblastoma (situation) Associated finding True Nephroblastoma Inferred relationship Some 1
Global developmental delay-lung cysts-overgrowth-Wilms tumor syndrome is a rare, genetic, overgrowth syndrome characterized by global developmental delay, macrosomia with subsequent somatic overgrowth, bilateral cystic lung lesions, congenital nephromegaly and bilateral Wilms tumor. Craniofacial dysmorphism includes macrocephaly, frontal bossing, large anterior fontanelle, mild hypertelorism, ear pit, flat nasal bridge, anteverted nares and mild micrognathia. Additional features may include brain and skeletal anomalies, enlarged protuberant abdomen, fat pads on dorsum of feet and toes, and rugated soles with skin folds, as well as umbilical/inguinal hernia and autistic behavior. Is a True Nephroblastoma Inferred relationship Some
Nephroblastoma of left kidney Is a True Nephroblastoma Inferred relationship Some
Nephroblastoma of right kidney Is a True Nephroblastoma Inferred relationship Some
Primary nephroblastoma (disorder) Is a True Nephroblastoma Inferred relationship Some

This concept is not in any reference sets

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