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4720007: Dystrophy (morphologic abnormality)


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
8873011 Dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
784632017 Dystrophy (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
8873011 Dystrophy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
8873011 Dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
784632017 Dystrophy (morphologic abnormality) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
784632017 Dystrophy (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


2 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Dystrophy Is a Degenerative abnormality (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group
Hyperplastic dystrophy (morphologic abnormality) Is a True Dystrophy Inferred relationship Existential restriction modifier (core metadata concept)
Pseudohypertrophic dystrophy Is a True Dystrophy Inferred relationship Existential restriction modifier (core metadata concept)
Lipodystrophy, partial, with Rieger anomaly, short stature, and insulinopenic diabetes mellitus (disorder) Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
Acrorenal field defect, ectodermal dysplasia, and lipoatrophic diabetes Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
Mucopolysaccharidosis, MPS-IV-B Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept)
Median nail dystrophy of Heller Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital myotonic dystrophy Associated morphology True Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Squamous cell hyperplasia of vulva (disorder) Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital total lipodystrophy (disorder) Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
Bietti's crystalline retinopathy Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Hair dystrophy (disorder) Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Primary hair dystrophy Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Secondary hair dystrophy Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Idiopathic hair dystrophy Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Lipoatrophic diabetes Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
syndrome douloureux régional complexe de type 1 Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Late-infantile neuronal ceroid lipofuscinosis Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept)
Lichen sclerosus et atrophicus of the vulva Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
Robinson nail dystrophy-deafness syndrome Associated morphology True Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Dilated cardiomyopathy secondary to myotonic dystrophy Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept)
Schwartz-Jampel syndrome Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept)
Morquio syndrome (disorder) Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept)
Neuronal ceroid lipofuscinosis Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept)
Hepatosis dietetica Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept)
Familial partial lipodystrophy Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
algodystrophie Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Dystrophy of vulva Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Infantile neuronal ceroid lipofuscinosis (disorder) Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept)
Juvenile neuronal ceroid lipofuscinosis (disorder) Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept)
Adult neuronal ceroid lipofuscinosis Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept)
Lipodystrophy Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Mucopolysaccharidosis IV-A (disorder) Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept)
Cutis laxa with osteodystrophy Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Jeune thoracic dystrophy (disorder) Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept)
Acquired partial lipodystrophy Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
Steinert myotonic dystrophy syndrome Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
chondrodystrophie malacique Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Median nail dystrophy Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Acquired generalized lipodystrophy Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
Partial face-sparing lipodystrophy Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
Lipodystrophy NOS Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
Dystrophy of vulva NOS Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Membranous lipodystrophy Associated morphology True Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
Median canaliform nail dystrophy Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Dystrophic cardiomyopathy (disorder) Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Fuchs' corneal dystrophy (disorder) Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Irido-corneo-endothelial syndrome Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Polymorphous corneal dystrophy Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Chandler syndrome Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
chondrodystrophie malacique Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 3
chondrodystrophie malacique Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
lipoatrophie congénitale généralisée Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
chondrodystrophie malacique Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
Distal muscular dystrophy with juvenile onset Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Muscular dystrophy with predominantly proximal limb girdle distribution Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
X-linked muscular dystrophy with limb girdle distribution Associated morphology True Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
X-linked muscular dystrophy with abnormal dystrophin (disorder) Associated morphology True Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Intermediate X-linked muscular dystrophy Associated morphology True Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Manifesting female carrier of X-linked muscular dystrophy Associated morphology True Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
X-linked limb girdle muscular dystrophy with normal dystrophin Associated morphology True Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Ji muscular dystrophy Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary myopathy limited to females Associated morphology True Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal recessive muscular dystrophy with limb girdle distribution (disorder) Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal recessive muscular dystrophy with abnormal dystrophin-associated glycoprotein Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Severe autosomal recessive muscular dystrophy of childhood - North African type Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal recessive muscular dystrophy with gene located at 15q Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Reunion-Indiana Amish type muscular dystrophy Associated morphology True Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital muscular dystrophy Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Western type of congenital muscular dystrophy Associated morphology True Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital muscular dystrophy with arthrogryposis multiplex congenita Associated morphology True Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Ullrich congenital muscular dystrophy Associated morphology True Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Eichsfeld type congenital muscular dystrophy Associated morphology True Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Hutterite type of muscular dystrophy (disorder) Associated morphology True Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Adult onset autosomal recessive muscular dystrophy with normal dystrophin Associated morphology True Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal dominant muscular dystrophy with limb girdle distribution Associated morphology True Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal dominant muscular dystrophy with gene located at 5q31 Associated morphology True Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Late onset proximal muscular dystrophy with dysarthria Associated morphology True Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Muscular dystrophy not predominantly limb girdle in distribution Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
X-linked muscular dystrophy not predominantly limb girdle Associated morphology True Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Benign scapuloperoneal muscular dystrophy with cardiomyopathy Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal recessive muscular dystrophy not predominantly limb girdle Associated morphology True Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Scapulohumeral muscular dystrophy (disorder) Associated morphology True Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal dominant muscular dystrophy not predominantly limb girdle (disorder) Associated morphology True Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Benign scapuloperoneal muscular dystrophy Associated morphology True Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Severe scapuloperoneal muscular dystrophy with cardiomyopathy Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Benign congenital muscular dystrophy with finger flexion contractures Associated morphology True Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Distal muscular dystrophy with adult onset Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Muscular dystrophy-deafmutism syndrome Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hereditary muscular dystrophy Associated morphology True Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Fukuyama congenital muscular dystrophy Associated morphology True Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Merosin deficient congenital muscular dystrophy Associated morphology True Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Walker-Warburg congenital muscular dystrophy Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 3
Muscle-eye-brain disease, congenital muscular dystrophy Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
Distal muscular dystrophy, Miyoshi type Associated morphology True Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Emery-Dreifuss muscular dystrophy Associated morphology True Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Severe childhood autosomal recessive muscular dystrophy Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital muscular hypertrophy-cerebral syndrome Associated morphology True Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Distal muscular dystrophy Associated morphology True Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
dystrophie musculaire oculaire Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Muscular dystrophy Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Oculopharyngeal muscular dystrophy Associated morphology False Dystrophy Inferred relationship Existential restriction modifier (core metadata concept) 1

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