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240048000: X-linked muscular dystrophy with abnormal dystrophin (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
359642016 X-linked muscular dystrophy with abnormal dystrophin en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
359643014 Meryon muscular dystrophy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
359644015 Xp21-linked muscular dystrophy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
629138013 X-linked muscular dystrophy with abnormal dystrophin (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
359642016 X-linked muscular dystrophy with abnormal dystrophin en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
359643014 Meryon muscular dystrophy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
359644015 Xp21-linked muscular dystrophy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
359644015 Xp21-linked muscular dystrophy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
629138013 X-linked muscular dystrophy with abnormal dystrophin (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
629138013 X-linked muscular dystrophy with abnormal dystrophin (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
5036151000241111 dystrophie musculaire liée au chromosome X avec dystrophine anormale fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5036151000241111 dystrophie musculaire liée au chromosome X avec dystrophine anormale fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

5 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
X-linked muscular dystrophy with abnormal dystrophin (disorder) Is a X-linked muscular dystrophy with limb girdle distribution true Inferred relationship Existential restriction modifier (core metadata concept)
X-linked muscular dystrophy with abnormal dystrophin (disorder) Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
X-linked muscular dystrophy with abnormal dystrophin (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 2
X-linked muscular dystrophy with abnormal dystrophin (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
X-linked muscular dystrophy with abnormal dystrophin (disorder) Associated morphology Dystrophy true Inferred relationship Existential restriction modifier (core metadata concept) 1
X-linked muscular dystrophy with abnormal dystrophin (disorder) Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
X-linked muscular dystrophy with abnormal dystrophin (disorder) Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
X-linked muscular dystrophy with abnormal dystrophin (disorder) Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
X-linked muscular dystrophy with abnormal dystrophin (disorder) Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
X-linked muscular dystrophy with abnormal dystrophin (disorder) Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
X-linked muscular dystrophy with abnormal dystrophin (disorder) Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
X-linked muscular dystrophy with abnormal dystrophin (disorder) Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
X-linked muscular dystrophy with abnormal dystrophin (disorder) Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
X-linked muscular dystrophy with abnormal dystrophin (disorder) Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
X-linked muscular dystrophy with abnormal dystrophin (disorder) Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
X-linked muscular dystrophy with abnormal dystrophin (disorder) Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
X-linked muscular dystrophy with abnormal dystrophin (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
X-linked muscular dystrophy with abnormal dystrophin (disorder) Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 3
X-linked muscular dystrophy with abnormal dystrophin (disorder) Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
X-linked muscular dystrophy with abnormal dystrophin (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
X-linked muscular dystrophy with abnormal dystrophin (disorder) Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
X-linked muscular dystrophy with abnormal dystrophin (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 2
X-linked muscular dystrophy with abnormal dystrophin (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
X-linked muscular dystrophy with abnormal dystrophin (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
X-linked muscular dystrophy with abnormal dystrophin (disorder) Clinical course Progressive true Inferred relationship Existential restriction modifier (core metadata concept) 2
Inbound Relationships Type Active Source Characteristic Refinability Group
Intermediate X-linked muscular dystrophy Is a True X-linked muscular dystrophy with abnormal dystrophin (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Manifesting female carrier of X-linked muscular dystrophy Is a True X-linked muscular dystrophy with abnormal dystrophin (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Becker muscular dystrophy Is a False X-linked muscular dystrophy with abnormal dystrophin (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Duchenne muscular dystrophy Is a True X-linked muscular dystrophy with abnormal dystrophin (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Becker muscular dystrophy (disorder) Is a True X-linked muscular dystrophy with abnormal dystrophin (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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