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240053005: Hereditary myopathy limited to females (disorder)

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
359649013 Hereditary myopathy limited to females en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
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 Only initial character 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
5036231000241112 myopathie héréditaire atteignant uniquement les femmes fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5036231000241112 myopathie héréditaire atteignant uniquement les femmes fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

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 Existential restriction modifier (core metadata concept)
Hereditary myopathy limited to females Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary myopathy limited to females Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary myopathy limited to females Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 2
Hereditary myopathy limited to females Associated morphology Dystrophy true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary myopathy limited to females Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Hereditary myopathy limited to females Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary myopathy limited to females Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Hereditary myopathy limited to females Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Hereditary myopathy limited to females Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary myopathy limited to females Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Hereditary myopathy limited to females Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary myopathy limited to females Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary myopathy limited to females Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Hereditary myopathy limited to females Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary myopathy limited to females Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Hereditary myopathy limited to females Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
Hereditary myopathy limited to females Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 3
Hereditary myopathy limited to females Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
Hereditary myopathy limited to females Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Hereditary myopathy limited to females Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Hereditary myopathy limited to females Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Hereditary myopathy limited to females Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary myopathy limited to females Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary myopathy limited to females Clinical course Progressive true Inferred relationship Existential restriction modifier (core metadata concept) 2
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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