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725420009: Congenital muscular dystrophy Paradas type (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3442512013 Congenital muscular dystrophy Paradas type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3442513015 Congenital muscular dystrophy Paradas type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3442514014 Congenital myopathy Paradas type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3442515010 An early-onset form of dysferlinopathy presenting with postnatal hypotonia, weakness in the proximal lower limbs and neck flexor muscles at birth and delayed motor development. To date, two cases have been described. The disease is caused by a mutation in the dysferlin gene (DYSF) coding for a protein involved in membrane repair. Transmission is autosomal recessive. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital muscular dystrophy Paradas type (disorder) survenue (attribut) congénital true Inferred relationship Some 1
Congenital muscular dystrophy Paradas type (disorder) localisation d'une constatation (attribut) structure de muscle squelettique true Inferred relationship Some 1
Congenital muscular dystrophy Paradas type (disorder) morphologie associée (attribut) Dystrophy (morphologic abnormality) true Inferred relationship Some 1
Congenital muscular dystrophy Paradas type (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Congenital muscular dystrophy Paradas type (disorder) est un(e) (attribut) Congenital hereditary muscular dystrophy true Inferred relationship Some
Congenital muscular dystrophy Paradas type (disorder) évolution clinique (attribut) progressif true Inferred relationship Some 2
Congenital muscular dystrophy Paradas type (disorder) est un(e) (attribut) Autosomal recessive hereditary disorder true Inferred relationship Some
Congenital muscular dystrophy Paradas type (disorder) est un(e) (attribut) Congenital muscular dystrophy false Inferred relationship Some
Congenital muscular dystrophy Paradas type (disorder) survenue (attribut) congénital false Inferred relationship Some 2
Congenital muscular dystrophy Paradas type (disorder) localisation d'une constatation (attribut) structure de muscle squelettique false Inferred relationship Some 2
Congenital muscular dystrophy Paradas type (disorder) survenue (attribut) congénital false Inferred relationship Some 3
Congenital muscular dystrophy Paradas type (disorder) localisation d'une constatation (attribut) structure de muscle squelettique false Inferred relationship Some 3
Congenital muscular dystrophy Paradas type (disorder) morphologie associée (attribut) Dystrophy (morphologic abnormality) false Inferred relationship Some 2
Congenital muscular dystrophy Paradas type (disorder) morphologie associée (attribut) Developmental abnormality false Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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