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193225000: Hereditary progressive muscular dystrophy (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
297608012 Hereditary progressive muscular dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3931000172112 dystrophie musculaire progressive héréditaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
524811000241112 dystrophie musculaire progressive héréditaire (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
577087018 Hereditary progressive muscular dystrophy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


114 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary progressive muscular dystrophy Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Hereditary progressive muscular dystrophy est un(e) (attribut) Hereditary disorder of musculoskeletal system true Inferred relationship Some
Hereditary progressive muscular dystrophy évolution clinique (attribut) progressif true Inferred relationship Some 2
Hereditary progressive muscular dystrophy est un(e) (attribut) Developmental hereditary disorder true Inferred relationship Some
Hereditary progressive muscular dystrophy morphologie associée (attribut) Dystrophy (morphologic abnormality) false Inferred relationship Some 1
Hereditary progressive muscular dystrophy est un(e) (attribut) Muscular dystrophy true Inferred relationship Some
Hereditary progressive muscular dystrophy morphologie associée (attribut) Dystrophy (morphologic abnormality) true Inferred relationship Some 1
Hereditary progressive muscular dystrophy localisation d'une constatation (attribut) structure de muscle squelettique true Inferred relationship Some 1
Hereditary progressive muscular dystrophy localisation d'une constatation (attribut) structure de muscle squelettique false Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
dystrophie musculaire distale est un(e) (attribut) True Hereditary progressive muscular dystrophy Inferred relationship Some
Muscular dystrophy with predominantly proximal limb girdle distribution est un(e) (attribut) True Hereditary progressive muscular dystrophy Inferred relationship Some
Congenital hereditary muscular dystrophy est un(e) (attribut) True Hereditary progressive muscular dystrophy Inferred relationship Some
X-linked scapuloperoneal muscular dystrophy (disorder) est un(e) (attribut) True Hereditary progressive muscular dystrophy Inferred relationship Some
Severe childhood autosomal recessive muscular dystrophy est un(e) (attribut) True Hereditary progressive muscular dystrophy Inferred relationship Some
Autosomal dominant Emery-Dreifuss muscular dystrophy (disorder) est un(e) (attribut) True Hereditary progressive muscular dystrophy Inferred relationship Some
Steinert myotonic dystrophy syndrome est un(e) (attribut) False Hereditary progressive muscular dystrophy Inferred relationship Some
Autosomal recessive Emery-Dreifuss muscular dystrophy est un(e) (attribut) True Hereditary progressive muscular dystrophy Inferred relationship Some
X-linked Emery-Dreifuss muscular dystrophy est un(e) (attribut) True Hereditary progressive muscular dystrophy Inferred relationship Some
X-linked myopathy with postural muscle atrophy (disorder) est un(e) (attribut) True Hereditary progressive muscular dystrophy Inferred relationship Some
Myotonic dystrophy (disorder) est un(e) (attribut) True Hereditary progressive muscular dystrophy Inferred relationship Some
Childhood-onset progressive contractures, limb girdle weakness, muscle dystrophy syndrome est un(e) (attribut) True Hereditary progressive muscular dystrophy Inferred relationship Some
Bethlem myopathy (disorder) est un(e) (attribut) False Hereditary progressive muscular dystrophy Inferred relationship Some
Adult-onset distal myopathy due to valosin containing protein mutation (disorder) est un(e) (attribut) False Hereditary progressive muscular dystrophy Inferred relationship Some

This concept is not in any reference sets

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