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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
92026018 Familial neoplastic disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
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 Only initial character 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
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 Existential restriction modifier (core metadata concept)
Familial neoplastic disease Is a Familial disease true Inferred relationship Existential restriction modifier (core metadata concept)
Familial neoplastic disease Associated morphology Neoplasm true Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial neoplastic disease Pathological process Neoplastic process false Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
Familial multiple tumor syndrome Is a False Familial neoplastic disease Inferred relationship Existential restriction modifier (core metadata concept)
Familial cancer of breast (disorder) Is a True Familial neoplastic disease Inferred relationship Existential restriction modifier (core metadata concept)
Familial atrial myxoma (disorder) Is a True Familial neoplastic disease Inferred relationship Existential restriction modifier (core metadata concept)
Li-Fraumeni syndrome (disorder) Is a True Familial neoplastic disease Inferred relationship Existential restriction modifier (core metadata concept)
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 Existential restriction modifier (core metadata concept)
Familial prostate cancer Is a True Familial neoplastic disease Inferred relationship Existential restriction modifier (core metadata concept)
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 Existential restriction modifier (core metadata concept)
Familial papillary thyroid carcinoma with renal papillary neoplasia syndrome (disorder) Is a True Familial neoplastic disease Inferred relationship Existential restriction modifier (core metadata concept)
Familial renal cell carcinoma (disorder) Is a True Familial neoplastic disease Inferred relationship Existential restriction modifier (core metadata concept)
fibrofolliculomes multiples familiaux Is a False Familial neoplastic disease Inferred relationship Existential restriction modifier (core metadata concept)
Familial malignant melanoma of skin Is a True Familial neoplastic disease Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary primary clear cell renal cell carcinoma (disorder) Is a False Familial neoplastic disease Inferred relationship Existential restriction modifier (core metadata concept)
Familial multiple benign meningioma Is a True Familial neoplastic disease Inferred relationship Existential restriction modifier (core metadata concept)
Ovarialkarzinom, lagespezifisches Is a False Familial neoplastic disease Inferred relationship Existential restriction modifier (core metadata concept)
Familial angiolipomatosis Is a True Familial neoplastic disease Inferred relationship Existential restriction modifier (core metadata concept)
Familial nonmedullary primary thyroid carcinoma (disorder) Is a True Familial neoplastic disease Inferred relationship Existential restriction modifier (core metadata concept)
Familial mastocytosis Is a True Familial neoplastic disease Inferred relationship Existential restriction modifier (core metadata concept)
Familial multiple leiomyoma cutis (disorder) Is a True Familial neoplastic disease Inferred relationship Existential restriction modifier (core metadata concept)
Familial multiple lipomata (disorder) Is a True Familial neoplastic disease Inferred relationship Existential restriction modifier (core metadata concept)
Familial ovarian cancer Is a True Familial neoplastic disease Inferred relationship Existential restriction modifier (core metadata concept)
Familial multiple discoid fibroma Is a True Familial neoplastic disease Inferred relationship Existential restriction modifier (core metadata concept)
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 Existential restriction modifier (core metadata concept)
Familial benign glomus tumor of skin Is a True Familial neoplastic disease Inferred relationship Existential restriction modifier (core metadata concept)
Familial cavernous malformation of spinal cord (disorder) Is a True Familial neoplastic disease Inferred relationship Existential restriction modifier (core metadata concept)

Reference Sets

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