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763314009: Congenital muscular dystrophy with hyperlaxity (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3638515012 Congenital muscular dystrophy with hyperlaxity (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3638516013 Congenital muscular dystrophy with hyperlaxity en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5404002012 Congenital muscular dystrophy with hyperlaxity is a rare, genetic neuromuscular disease characterized by congenital hypotonia, generalized, slowly progressive muscular weakness, and proximal joint contractures with distal joint hypermobility and hyperlaxity. Scoliosis or rigidity of the spine and delayed motor milestones are also frequently reported. Other manifestations include a long myopathic face and, in rare cases, respiratory failure, mild to moderate intellectual deficiency and short stature. Ambulation may be impaired with time. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5404003019 Congenital muscular dystrophy with hyperlaxity is a rare, genetic neuromuscular disease characterised by congenital hypotonia, generalised, slowly progressive muscular weakness, and proximal joint contractures with distal joint hypermobility and hyperlaxity. Scoliosis or rigidity of the spine and delayed motor milestones are also frequently reported. Other manifestations include a long myopathic face and, in rare cases, respiratory failure, mild to moderate intellectual deficiency and short stature. Ambulation may be impaired with time. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3638515012 Congenital muscular dystrophy with hyperlaxity (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3638516013 Congenital muscular dystrophy with hyperlaxity en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3638517016 A rare genetic neuromuscular disease characterized by congenital hypotonia, generalized, slowly progressive muscular weakness, and proximal joint contractures with distal joint hypermobility and hyperlaxity. Scoliosis or rigidity of the spine and delayed motor milestones are also frequently reported. Other manifestations include a long myopathic face and in rare cases, respiratory failure, mild to moderate intellectual deficiency and short stature. Ambulation may be impaired with time. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3638518014 A rare genetic neuromuscular disease characterised by congenital hypotonia, generalised, slowly progressive muscular weakness, and proximal joint contractures with distal joint hypermobility and hyperlaxity. Scoliosis or rigidity of the spine and delayed motor milestones are also frequently reported. Other manifestations include a long myopathic face and in rare cases, respiratory failure, mild to moderate intellectual deficiency and short stature. Ambulation may be impaired with time. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5404002012 Congenital muscular dystrophy with hyperlaxity is a rare, genetic neuromuscular disease characterized by congenital hypotonia, generalized, slowly progressive muscular weakness, and proximal joint contractures with distal joint hypermobility and hyperlaxity. Scoliosis or rigidity of the spine and delayed motor milestones are also frequently reported. Other manifestations include a long myopathic face and, in rare cases, respiratory failure, mild to moderate intellectual deficiency and short stature. Ambulation may be impaired with time. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5404003019 Congenital muscular dystrophy with hyperlaxity is a rare, genetic neuromuscular disease characterised by congenital hypotonia, generalised, slowly progressive muscular weakness, and proximal joint contractures with distal joint hypermobility and hyperlaxity. Scoliosis or rigidity of the spine and delayed motor milestones are also frequently reported. Other manifestations include a long myopathic face and, in rare cases, respiratory failure, mild to moderate intellectual deficiency and short stature. Ambulation may be impaired with time. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3386931001000113 Kongenitale Muskeldystrophie mit Gelenkinstabilität de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
940051000172110 CMDH - congenital muscular dystrophy with hyperlaxity fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
965441000172118 dystrophie musculaire congénitale avec hyperlaxité fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
940051000172110 CMDH - congenital muscular dystrophy with hyperlaxity fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
965441000172118 dystrophie musculaire congénitale avec hyperlaxité fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3386931001000113 Kongenitale Muskeldystrophie mit Gelenkinstabilität 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
Congenital muscular dystrophy with hyperlaxity (disorder) Is a Congenital muscular dystrophy false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital muscular dystrophy with hyperlaxity (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital muscular dystrophy with hyperlaxity (disorder) Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital muscular dystrophy with hyperlaxity (disorder) Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital muscular dystrophy with hyperlaxity (disorder) Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital muscular dystrophy with hyperlaxity (disorder) Associated morphology Dystrophy true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital muscular dystrophy with hyperlaxity (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital muscular dystrophy with hyperlaxity (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital muscular dystrophy with hyperlaxity (disorder) Is a Congenital hereditary muscular dystrophy true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital muscular dystrophy with hyperlaxity (disorder) Clinical course Progressive true Inferred relationship Existential restriction modifier (core metadata concept) 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

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

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