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778050009: Idiopathic eosinophilic myositis (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5405589017 A rare idiopathic inflammatory myopathy characterized by eosinophilic infiltration and inflammatory lesions of the skeletal muscle tissue, in the absence of an identifiable causative factor (e.g. parasitic infection, drug intake, systemic or malignant disease). Clinically patients may present focal or generalized muscle weakness and pain, difficulties to walk, motor clumsiness and/or mild bilateral Achilles tendon contracture, as well as elevated serum creatine kinase levels and peripheral blood and/or bone marrow hypereosinophilia. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5405590014 A rare idiopathic inflammatory myopathy characterised by eosinophilic infiltration and inflammatory lesions of the skeletal muscle tissue, in the absence of an identifiable causative factor (e.g. parasitic infection, drug intake, systemic or malignant disease). Clinically patients may present focal or generalised muscle weakness and pain, difficulties to walk, motor clumsiness and/or mild bilateral Achilles tendon contracture, as well as elevated serum creatine kinase levels and peripheral blood and/or bone marrow hypereosinophilia. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3737512012 Idiopathic eosinophilic myositis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3737513019 Idiopathic eosinophilia-associated myopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3737514013 Idiopathic eosinophilic myositis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
878241000172112 myosite éosinophile idiopathique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3433671001000111 Idiopathische eosinophile Myositis 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
A rare idiopathic inflammatory myopathy characterized by eosinophilic infiltration and inflammatory lesions of the skeletal muscle tissue, in the absence of an identifiable causative factor (e.g. parasitic infection, drug intake, systemic or malignant disease). Clinically patients may present focal or generalized muscle weakness and pain, difficulties to walk, motor clumsiness and/or mild bilateral Achilles tendon contracture, as well as elevated serum creatine kinase levels and peripheral blood and/or bone marrow hypereosinophilia. Associated morphology Chronic eosinophilic inflammation true Inferred relationship Some 1
A rare idiopathic inflammatory myopathy characterized by eosinophilic infiltration and inflammatory lesions of the skeletal muscle tissue, in the absence of an identifiable causative factor (e.g. parasitic infection, drug intake, systemic or malignant disease). Clinically patients may present focal or generalized muscle weakness and pain, difficulties to walk, motor clumsiness and/or mild bilateral Achilles tendon contracture, as well as elevated serum creatine kinase levels and peripheral blood and/or bone marrow hypereosinophilia. Is a Idiopathic disease false Inferred relationship Some
A rare idiopathic inflammatory myopathy characterized by eosinophilic infiltration and inflammatory lesions of the skeletal muscle tissue, in the absence of an identifiable causative factor (e.g. parasitic infection, drug intake, systemic or malignant disease). Clinically patients may present focal or generalized muscle weakness and pain, difficulties to walk, motor clumsiness and/or mild bilateral Achilles tendon contracture, as well as elevated serum creatine kinase levels and peripheral blood and/or bone marrow hypereosinophilia. Is a Eosinophilic myositis (disorder) true Inferred relationship Some
A rare idiopathic inflammatory myopathy characterized by eosinophilic infiltration and inflammatory lesions of the skeletal muscle tissue, in the absence of an identifiable causative factor (e.g. parasitic infection, drug intake, systemic or malignant disease). Clinically patients may present focal or generalized muscle weakness and pain, difficulties to walk, motor clumsiness and/or mild bilateral Achilles tendon contracture, as well as elevated serum creatine kinase levels and peripheral blood and/or bone marrow hypereosinophilia. Finding site Skeletal muscle structure true Inferred relationship Some 1
A rare idiopathic inflammatory myopathy characterized by eosinophilic infiltration and inflammatory lesions of the skeletal muscle tissue, in the absence of an identifiable causative factor (e.g. parasitic infection, drug intake, systemic or malignant disease). Clinically patients may present focal or generalized muscle weakness and pain, difficulties to walk, motor clumsiness and/or mild bilateral Achilles tendon contracture, as well as elevated serum creatine kinase levels and peripheral blood and/or bone marrow hypereosinophilia. Is a Idiopathic inflammatory myopathy (disorder) true Inferred relationship Some
A rare idiopathic inflammatory myopathy characterized by eosinophilic infiltration and inflammatory lesions of the skeletal muscle tissue, in the absence of an identifiable causative factor (e.g. parasitic infection, drug intake, systemic or malignant disease). Clinically patients may present focal or generalized muscle weakness and pain, difficulties to walk, motor clumsiness and/or mild bilateral Achilles tendon contracture, as well as elevated serum creatine kinase levels and peripheral blood and/or bone marrow hypereosinophilia. Pathological process (attribute) Abnormal immune process (qualifier value) true Inferred relationship Some 1
A rare idiopathic inflammatory myopathy characterized by eosinophilic infiltration and inflammatory lesions of the skeletal muscle tissue, in the absence of an identifiable causative factor (e.g. parasitic infection, drug intake, systemic or malignant disease). Clinically patients may present focal or generalized muscle weakness and pain, difficulties to walk, motor clumsiness and/or mild bilateral Achilles tendon contracture, as well as elevated serum creatine kinase levels and peripheral blood and/or bone marrow hypereosinophilia. Has interpretation Above reference range true Inferred relationship Some 2
A rare idiopathic inflammatory myopathy characterized by eosinophilic infiltration and inflammatory lesions of the skeletal muscle tissue, in the absence of an identifiable causative factor (e.g. parasitic infection, drug intake, systemic or malignant disease). Clinically patients may present focal or generalized muscle weakness and pain, difficulties to walk, motor clumsiness and/or mild bilateral Achilles tendon contracture, as well as elevated serum creatine kinase levels and peripheral blood and/or bone marrow hypereosinophilia. Interprets Eosinophil count true Inferred relationship Some 2
A rare idiopathic inflammatory myopathy characterized by eosinophilic infiltration and inflammatory lesions of the skeletal muscle tissue, in the absence of an identifiable causative factor (e.g. parasitic infection, drug intake, systemic or malignant disease). Clinically patients may present focal or generalized muscle weakness and pain, difficulties to walk, motor clumsiness and/or mild bilateral Achilles tendon contracture, as well as elevated serum creatine kinase levels and peripheral blood and/or bone marrow hypereosinophilia. Is a Idiopathic eosinophilia true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

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

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