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397016004: Systemic mast cell disease (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1764934017 Systemic mast cell disease (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1776751015 Systemic mast cell disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1785705017 Systemic mastocytosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1785706016 SMCD - systemic mast cell disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
1860851000195111 mastocitosi sistemica it Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5251521000241112 mastocytose systémique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3429231001000110 Mastozytose, systemische de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


9 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Systemic mast cell disease (disorder) Is a Mast cell disorder (disorder) false Inferred relationship Some
Systemic mast cell disease (disorder) Finding site Leukocyte false Inferred relationship Some
Systemic mast cell disease (disorder) Finding site Hematopoietic system structure false Inferred relationship Some
Systemic mast cell disease (disorder) Finding site Structure of immune system (body structure) false Inferred relationship Some
Systemic mast cell disease (disorder) Associated morphology Mast cell abnormality (morphologic abnormality) false Inferred relationship Some 1
Systemic mast cell disease (disorder) Associated morphology White blood cell abnormality false Inferred relationship Some
Systemic mast cell disease (disorder) Has definitional manifestation White blood cell finding false Inferred relationship Some
Systemic mast cell disease (disorder) Has definitional manifestation Immune system finding false Inferred relationship Some
Systemic mast cell disease (disorder) Has definitional manifestation Immune system finding false Inferred relationship Some
Systemic mast cell disease (disorder) Pathological process (attribute) Abnormal immune process (qualifier value) false Inferred relationship Some 2
Systemic mast cell disease (disorder) Associated morphology Hyperplasia false Inferred relationship Some 1
Systemic mast cell disease (disorder) Is a Systemic disease true Inferred relationship Some
Systemic mast cell disease (disorder) Finding site Mast cell (cell) false Inferred relationship Some 1
Systemic mast cell disease (disorder) Pathological process (attribute) Abnormal immune process (qualifier value) false Inferred relationship Some 1
Systemic mast cell disease (disorder) Associated morphology Mastocytosis true Inferred relationship Some 1
Systemic mast cell disease (disorder) Is a Mast cell neoplasm (disorder) true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Mast cell leukaemia (clinical) Is a False Systemic mast cell disease (disorder) Inferred relationship Some
Indolent systemic mastocytosis Is a True Systemic mast cell disease (disorder) Inferred relationship Some
Aggressive lymphadenopathic mastocytosis with eosinophilia (disorder) Is a False Systemic mast cell disease (disorder) Inferred relationship Some
Systemic mastocytosis with associated clonal hematological non-mast cell lineage disease (disorder) Is a False Systemic mast cell disease (disorder) Inferred relationship Some
A rare, aggressive form of advanced systemic mastocytosis (advSM) characterized by massive infiltration of mast cells (MC) in different tissues and presence of extracutaneous organ dysfunction, but without evidence of mast cell leukemia or another hematologic neoplasm. Is a False Systemic mast cell disease (disorder) Inferred relationship Some
leucémie mastocytaire aleucémique Is a False Systemic mast cell disease (disorder) Inferred relationship Some
leucémie mastocytaire classique Is a False Systemic mast cell disease (disorder) Inferred relationship Some
Malignant mastocytosis Is a True Systemic mast cell disease (disorder) Inferred relationship Some
A rare, slowly progressive form of systemic mastocytosis (SM) characterized by gradual accumulation of neoplastic mast cells in the visceral organs. Patients typically present with splenomegaly, hypercellular marrow and, in most cases, urticaria pigmentosa-like skin lesions. Is a False Systemic mast cell disease (disorder) Inferred relationship Some
A rare subtype of indolent systemic mastocytosis characterized by isolated bone marrow involvement without skin lesions, low burden of neoplastic mast cells, and often normal or near normal serum tryptase levels. The KIT D816V mutation is present in the majority of cases. Is a True Systemic mast cell disease (disorder) Inferred relationship Some

This concept is not in any reference sets

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