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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
577087018 Hereditary progressive muscular dystrophy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3257651000005110 hereditær progredierende muskeldystrofi da Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) dansk modul

117 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary progressive muscular dystrophy Is a Muscular dystrophy true Inferred relationship Some
Hereditary progressive muscular dystrophy Finding site Skeletal muscle structure false Inferred relationship Some 1
Hereditary progressive muscular dystrophy Associated morphology Dystrophy false Inferred relationship Some 1
Hereditary progressive muscular dystrophy Associated morphology Dystrophy true Inferred relationship Some 1
Hereditary progressive muscular dystrophy Finding site Skeletal muscle structure true Inferred relationship Some 1
Hereditary progressive muscular dystrophy Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Hereditary progressive muscular dystrophy Is a Hereditary disorder of musculoskeletal system true Inferred relationship Some
Hereditary progressive muscular dystrophy Clinical course Progressive (qualifier value) true Inferred relationship Some 2
Hereditary progressive muscular dystrophy Is a Developmental hereditary disorder true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Bethlem myopathy (disorder) Is a False Hereditary progressive muscular dystrophy Inferred relationship Some
Adult-onset distal myopathy due to valosin containing protein mutation (disorder) Is a False Hereditary progressive muscular dystrophy Inferred relationship Some
Distal muscular dystrophy Is a True Hereditary progressive muscular dystrophy Inferred relationship Some
Muscular dystrophy with predominantly proximal limb girdle distribution Is a True Hereditary progressive muscular dystrophy Inferred relationship Some
Congenital hereditary muscular dystrophy Is a True Hereditary progressive muscular dystrophy Inferred relationship Some
X-linked scapuloperoneal muscular dystrophy (disorder) Is a True Hereditary progressive muscular dystrophy Inferred relationship Some
Severe childhood autosomal recessive muscular dystrophy Is a True Hereditary progressive muscular dystrophy Inferred relationship Some
Autosomal dominant Emery-Dreifuss muscular dystrophy (disorder) Is a True Hereditary progressive muscular dystrophy Inferred relationship Some
Steinert myotonic dystrophy syndrome Is a False Hereditary progressive muscular dystrophy Inferred relationship Some
Autosomal recessive Emery-Dreifuss muscular dystrophy Is a True Hereditary progressive muscular dystrophy Inferred relationship Some
X-linked Emery-Dreifuss muscular dystrophy Is a True Hereditary progressive muscular dystrophy Inferred relationship Some
X-linked myopathy with postural muscle atrophy (disorder) Is a True Hereditary progressive muscular dystrophy Inferred relationship Some
Myotonic dystrophy (disorder) Is a True Hereditary progressive muscular dystrophy Inferred relationship Some
Childhood-onset progressive contractures, limb girdle weakness, muscle dystrophy syndrome Is a True Hereditary progressive muscular dystrophy Inferred relationship Some

This concept is not in any reference sets

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