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774082004: Neonatal dermatomyositis (disorder)

Status: current, Not 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
3727906017 Neonatal dermatomyositis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3727907014 Neonatal dermatomyositis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3727908016 A very rare secondary neonatal autoimmune disease characterised by generalised weakness, severe hypotonia, absent or reduced deep tendon reflexes and highly elevated serum creatine kinase levels presenting in the neonatal period. Perifascicular atrophy in the presence of a diffuse perivascular inflammatory cell exudate is observed on muscle biopsy. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3727909012 A very rare secondary neonatal autoimmune disease characterized by generalized weakness, severe hypotonia, absent or reduced deep tendon reflexes and highly elevated serum creatine kinase levels presenting in the neonatal period. Perifascicular atrophy in the presence of a diffuse perivascular inflammatory cell exudate is observed on muscle biopsy. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3727906017 Neonatal dermatomyositis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3727907014 Neonatal dermatomyositis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3727908016 A very rare secondary neonatal autoimmune disease characterised by generalised weakness, severe hypotonia, absent or reduced deep tendon reflexes and highly elevated serum creatine kinase levels presenting in the neonatal period. Perifascicular atrophy in the presence of a diffuse perivascular inflammatory cell exudate is observed on muscle biopsy. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3727909012 A very rare secondary neonatal autoimmune disease characterized by generalized weakness, severe hypotonia, absent or reduced deep tendon reflexes and highly elevated serum creatine kinase levels presenting in the neonatal period. Perifascicular atrophy in the presence of a diffuse perivascular inflammatory cell exudate is observed on muscle biopsy. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3384921001000118 Dermatomyositis, neonatale de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
920371000172119 dermatomyosite néonatale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
1013981000172114 DM (dermatomyosite) néonatale fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
920371000172119 dermatomyosite néonatale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
1013981000172114 DM (dermatomyosite) néonatale fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3384921001000118 Dermatomyositis, neonatale 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
Neonatal dermatomyositis (disorder) Is a Autoimmune inflammation of skeletal muscle (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Neonatal dermatomyositis (disorder) Associated morphology inflammation false Inferred relationship Existential restriction modifier (core metadata concept) 1
Neonatal dermatomyositis (disorder) Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Neonatal dermatomyositis (disorder) Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Neonatal dermatomyositis (disorder) Occurrence Neonatal true Inferred relationship Existential restriction modifier (core metadata concept) 2
Neonatal dermatomyositis (disorder) Associated morphology inflammation false Inferred relationship Existential restriction modifier (core metadata concept) 2
Neonatal dermatomyositis (disorder) Is a Autoimmune skin disease true Inferred relationship Existential restriction modifier (core metadata concept)
Neonatal dermatomyositis (disorder) Occurrence Neonatal true Inferred relationship Existential restriction modifier (core metadata concept) 1
Neonatal dermatomyositis (disorder) Is a Dermatomyositis (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Neonatal dermatomyositis (disorder) Pathological process (attribute) Autoimmune process true Inferred relationship Existential restriction modifier (core metadata concept) 1
Neonatal dermatomyositis (disorder) Pathological process (attribute) Autoimmune process true Inferred relationship Existential restriction modifier (core metadata concept) 2
Neonatal dermatomyositis (disorder) Is a Neonatal disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Neonatal dermatomyositis (disorder) Finding site Skin structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Neonatal dermatomyositis (disorder) Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Neonatal dermatomyositis (disorder) Associated morphology Inflammatory morphology (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Neonatal dermatomyositis (disorder) Associated morphology Inflammatory morphology (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Neonatal dermatomyositis (disorder) Is a Dermatitis of the newborn (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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