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240053005: hereditaire myopathie beperkt tot vrouwen (aandoening)


Status: current, Not 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
359649013 Hereditary myopathy limited to females en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
629143018 Hereditary myopathy limited to females (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
6126251000146112 hereditaire myopathie beperkt tot vrouwen nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6126261000146110 hereditaire myopathie beperkt tot vrouwen (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6126271000146116 erfelijke myopathie beperkt tot vrouwen nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6126281000146119 genetische myopathie beperkt tot vrouwen nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary myopathy limited to females Is a X-linked limb girdle muscular dystrophy with normal dystrophin true Inferred relationship Some
Hereditary myopathy limited to females Finding site Skeletal muscle structure false Inferred relationship Some 1
Hereditary myopathy limited to females Occurrence Congenital false Inferred relationship Some
Hereditary myopathy limited to females Associated morphology congenitale anomalie (afwijkende morfologie) false Inferred relationship Some 2
Hereditary myopathy limited to females Associated morphology Dystrophy true Inferred relationship Some 1
Hereditary myopathy limited to females Finding site Skeletal muscle structure false Inferred relationship Some 2
Hereditary myopathy limited to females Finding site Skeletal muscle structure false Inferred relationship Some 1
Hereditary myopathy limited to females Finding site Skeletal muscle structure false Inferred relationship Some 2
Hereditary myopathy limited to females Finding site Skeletal muscle structure false Inferred relationship Some 2
Hereditary myopathy limited to females Finding site Skeletal muscle structure false Inferred relationship Some 1
Hereditary myopathy limited to females Finding site Skeletal muscle structure false Inferred relationship Some 2
Hereditary myopathy limited to females Finding site Skeletal muscle structure false Inferred relationship Some 1
Hereditary myopathy limited to females Finding site Skeletal muscle structure false Inferred relationship Some 1
Hereditary myopathy limited to females Finding site Skeletal muscle structure false Inferred relationship Some 2
Hereditary myopathy limited to females Finding site Skeletal muscle structure true Inferred relationship Some 1
Hereditary myopathy limited to females Finding site Skeletal muscle structure false Inferred relationship Some 2
Hereditary myopathy limited to females Occurrence Congenital false Inferred relationship Some 3
Hereditary myopathy limited to females Associated morphology gebrekkige ontwikkeling (afwijkende morfologie) false Inferred relationship Some 3
Hereditary myopathy limited to females Finding site Skeletal muscle structure false Inferred relationship Some 3
Hereditary myopathy limited to females Occurrence Congenital false Inferred relationship Some 2
Hereditary myopathy limited to females Associated morphology Morphologically abnormal structure (morphologic abnormality) false Inferred relationship Some 2
Hereditary myopathy limited to females Pathological process (attribute) Pathological developmental process false Inferred relationship Some 2
Hereditary myopathy limited to females Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Hereditary myopathy limited to females Occurrence Congenital true Inferred relationship Some 1
Hereditary myopathy limited to females Clinical course Progressive (qualifier value) true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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