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55352002: Familial neoplastic disease (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
92026018 Familial neoplastic disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
793695014 Familial neoplastic disease (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
125881000077114 néoplasie familiale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

21 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial neoplastic disease Is a Neoplastic disease true Inferred relationship Some
Familial neoplastic disease Is a Familial disease true Inferred relationship Some
Familial neoplastic disease Associated morphology Neoplasm true Inferred relationship Some 1
Familial neoplastic disease Pathological process Neoplastic process false Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Familial multiple tumor syndrome Is a False Familial neoplastic disease Inferred relationship Some
Familial cancer of breast Is a True Familial neoplastic disease Inferred relationship Some
Familial atrial myxoma (disorder) Is a True Familial neoplastic disease Inferred relationship Some
Li-Fraumeni syndrome (disorder) Is a True Familial neoplastic disease Inferred relationship Some
A rare familial renal cancer syndrome characterized by a predisposition for developing bilateral and multifocal classic type papillary renal cell carcinomas (formerly known as type 1 papillary renal cell carcinoma until the 2022 WHO classification of renal tumors). Is a False Familial neoplastic disease Inferred relationship Some
Familial prostate cancer (FPC) is a malignant tumor of the prostate with an early onset. FPC is either asymptomatic or causes micturition symptoms, erectile dysfunction, bone pain, venous compression and infectious or inflammatory syndrome (for the metastatic forms). It is also characterized by familial antecedents. Is a True Familial neoplastic disease Inferred relationship Some
Defined by the presence of pancreatic cancer in two or more first-degree relatives. In familial cases, disease onset occurs before 50 years of age, earlier than for the other forms of pancreatic cancer. Prognosis is poor. Is a True Familial neoplastic disease Inferred relationship Some
An extremely rare inherited tumor syndrome within the familial nonmedullary thyroid cancer group. Is a True Familial neoplastic disease Inferred relationship Some
Familial renal cell carcinoma (disorder) Is a True Familial neoplastic disease Inferred relationship Some
fibrofolliculomes multiples familiaux Is a False Familial neoplastic disease Inferred relationship Some
Familial melanoma (FM) is a rare inherited form of melanoma characterized by development of histologically confirmed melanoma in two first degree relatives or more relatives in an affected family. Is a True Familial neoplastic disease Inferred relationship Some
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. Is a False Familial neoplastic disease Inferred relationship Some
Familial multiple meningioma is a rare, benign neoplasm of the central nervous system characterized by the development of multiple or, rarely, solitary meningiomas in two or more blood relatives, without other apparent syndromic manifestations. Depending on the localization, growth rate and size of the tumors, patients can present with subtle, gradually worsening or abrupt and severe neurological compromise or can be completely asymptomatic. Is a True Familial neoplastic disease Inferred relationship Some
syndrome héréditaire de prédisposition au cancer de l'ovaire Is a False Familial neoplastic disease Inferred relationship Some
Familial angiolipomatosis is a rare, genetic, subcutaneous tissue disorder characterized by the presence of benign, usually multiple, subcutaneous tumors composed of adipose tissue and blood vessels, typically manifesting as yellow, firm, circumscribed, 1-4 cm in diameter tumors located in the arms, legs and trunk, with deep extension of the lesions between muscles, tendons and joint capsules (without infiltration of these structures), in several members of a single family. Tumors may be tender or mildly painful when palpated and do not regress spontaneously. Is a True Familial neoplastic disease Inferred relationship Some
Familial papillary or follicular thyroid carcinoma is a rare, hereditary nonmedullary thyroid carcinoma characterized by the presence of differentiated thyroid cancer of follicular cell origin in two or more first-degree relatives, in the absence of other familial tumor syndromes or radiation exposure. Frequent capsular invasion is observed. Biopsy reveals multicentric tumors with multiple adenomatous nodules with or without oxyphilia and follicular or papillary carcinoma histology. Is a True Familial neoplastic disease Inferred relationship Some
Familial mastocytosis (disorder) Is a True Familial neoplastic disease Inferred relationship Some
Familial multiple leiomyoma cutis (disorder) Is a True Familial neoplastic disease Inferred relationship Some
Familial multiple lipomata (disorder) Is a True Familial neoplastic disease Inferred relationship Some
Familial ovarian cancer Is a True Familial neoplastic disease Inferred relationship Some
A rare, genetic, skin tumor disorder characterized by childhood-onset of multiple, benign, asymptomatic, white to flesh-colored papules predominantly located on the face, ears, neck and trunk, not associated with systemic organ involvement, malignancies or FLCN gene locus mutation. Is a True Familial neoplastic disease Inferred relationship Some
A rare neoplastic disease characterized by occurrence of atypical and aggressive gastric type 1 neuroendocrine tumors (NET) in early adulthood. The tumors often show nodal infiltration requiring total gastrectomy. Synchronous gastric adenocarcinoma has also been reported. Patients present high serum gastrin concentrations and iron-deficiency anemia (rather than megaloblastic anemia, which is a typical feature in patients with sporadic gastric type 1 NET, where the tumor usually arises on the background of autoimmune atrophic gastritis). Is a True Familial neoplastic disease Inferred relationship Some
Familial benign glomus tumour of skin Is a True Familial neoplastic disease Inferred relationship Some
Familial cavernous malformation of spinal cord (disorder) Is a True Familial neoplastic disease Inferred relationship Some

This concept is not in any reference sets

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