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255314001: Progressive (qualifier value)

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
138851000077114 progressif fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
380497019 Progressive en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
411831000077116 progressif (valeur de l'attribut) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
646336011 Progressive (qualifier value) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
progressif est un(e) (attribut) descripteurs de comportement true Inferred relationship Some
progressif est un(e) (attribut) chronique true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Steinert myotonic dystrophy syndrome évolution clinique (attribut) True progressif Inferred relationship Some 2
Reunion Island Larsen-like syndrome (disorder) évolution clinique (attribut) False progressif Inferred relationship Some 4
dysplasie épiphysaire multiple type 1 évolution clinique (attribut) True progressif Inferred relationship Some 2
Diastrophic dysplasia (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
dystrophie musculaire d'Emery-Dreifuss évolution clinique (attribut) True progressif Inferred relationship Some 2
Multiple epiphyseal dysplasia type 5 (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
Multiple dislocations with dysplasia évolution clinique (attribut) True progressif Inferred relationship Some 3
syndrome de dystrophie musculaire ménopausique évolution clinique (attribut) False progressif Inferred relationship Some 2
Desbuquois syndrome évolution clinique (attribut) True progressif Inferred relationship Some 3
Spondyloepimetaphyseal dysplasia with joint laxity évolution clinique (attribut) True progressif Inferred relationship Some 3
Larsen-like osseous dysplasia, short stature syndrome (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
Multiple epiphyseal dysplasia tarda type IIIa évolution clinique (attribut) True progressif Inferred relationship Some 2
Progressive systemic sclerosis (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
Distal myopathy 2 évolution clinique (attribut) True progressif Inferred relationship Some 3
Eiken syndrome (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
Ocular muscular dystrophy évolution clinique (attribut) False progressif Inferred relationship Some 2
Parana hard skin syndrome (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 1
Bethlem myopathy (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
Dementia paralytica juvenilis évolution clinique (attribut) True progressif Inferred relationship Some 3
Duchenne muscular dystrophy évolution clinique (attribut) True progressif Inferred relationship Some 3
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 6
syndrome de brachydactylie, mésomélie, déficience intellectuelle, malformation cardiaque évolution clinique (attribut) True progressif Inferred relationship Some 5
Osteochondrodysplasia with osteopetrosis (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 4
Osteopetrosis - intermediate type évolution clinique (attribut) True progressif Inferred relationship Some 3
dystrophie musculaire congénitale par déficit en intégrine alpha-7 évolution clinique (attribut) True progressif Inferred relationship Some 2
Osteopetrosis with renal tubular acidosis évolution clinique (attribut) True progressif Inferred relationship Some 3
Atelosteogenesis/diastrophic dysplasia évolution clinique (attribut) False progressif Inferred relationship Some 4
Scapuloperoneal muscular dystrophy évolution clinique (attribut) True progressif Inferred relationship Some 2
Progressive myoclonic epilepsy type 5 (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 1
Progressive myoclonic epilepsy type 3 évolution clinique (attribut) True progressif Inferred relationship Some 2
Autosomal recessive limb girdle muscular dystrophy type 2T (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
Congenital muscular dystrophy due to lamin A/C mutation (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
Autosomal recessive limb girdle muscular dystrophy type 2E (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
Atelosteogenesis type 1 (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
Atelosteogenesis type 3 (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
Epidermolysis bullosa simplex with muscular dystrophy (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
dysplasie spondylo-épimétaphysaire avec luxations multiples évolution clinique (attribut) True progressif Inferred relationship Some 3
Early onset myopathy with fatal cardiomyopathy (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
carpocyphose évolution clinique (attribut) True progressif Inferred relationship Some 4
Hereditary progressive muscular dystrophy évolution clinique (attribut) True progressif Inferred relationship Some 2
Dentin dysplasia with sclerotic bone syndrome évolution clinique (attribut) True progressif Inferred relationship Some 3
Carbohydrate sulfotransferase 3 related skeletal dysplasia (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
Craniometadiaphyseal dysplasia évolution clinique (attribut) True progressif Inferred relationship Some 2
Facioscapulohumeral muscular dystrophy (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
Congenital muscular dystrophy Paradas type (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
Charcot-Marie-Tooth disease type 2P (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
Osteomesopycnosis évolution clinique (attribut) False progressif Inferred relationship Some 2
Multiple epiphyseal dysplasia Lowry type (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
Mesomelic dysplasia Kantaputra type (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
Rhizomelic syndrome Urbach type évolution clinique (attribut) True progressif Inferred relationship Some 2
Juvenile onset Huntington's disease évolution clinique (attribut) True progressif Inferred relationship Some 2
Autosomal dominant Charcot-Marie-Tooth disease type 2O évolution clinique (attribut) True progressif Inferred relationship Some 3
Benign autosomal dominant osteopetrosis évolution clinique (attribut) True progressif Inferred relationship Some 3
Lower motor neuron syndrome with late-adult onset (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
Mesomelic dysplasia with cleft palate and camptodactyly syndrome (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 4
Mesomelic dysplasia of hypoplastic ulna and fibula type (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
Coxoauricular syndrome (disorder) évolution clinique (attribut) False progressif Inferred relationship Some 4
Manifesting female carrier of X-linked muscular dystrophy évolution clinique (attribut) True progressif Inferred relationship Some 2
Osteopetrosis évolution clinique (attribut) True progressif Inferred relationship Some 3
Hereditary myopathy limited to females évolution clinique (attribut) True progressif Inferred relationship Some 2
Peripheral neuropathy, myopathy, hoarseness, hearing loss syndrome évolution clinique (attribut) True progressif Inferred relationship Some 1
Adult-onset distal myopathy due to valosin containing protein mutation (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
Finnish upper limb onset distal myopathy évolution clinique (attribut) True progressif Inferred relationship Some 3
Distal nebulin myopathy évolution clinique (attribut) True progressif Inferred relationship Some 1
Congenital muscular dystrophy with intellectual disability and severe epilepsy évolution clinique (attribut) True progressif Inferred relationship Some 3
Reunion-Indiana Amish type muscular dystrophy évolution clinique (attribut) True progressif Inferred relationship Some 2
Multiple epiphyseal dysplasia Beighton type (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
Segmental progressive overgrowth syndrome with fibroadipose hyperplasia évolution clinique (attribut) True progressif Inferred relationship Some 3
Ullrich congenital muscular dystrophy évolution clinique (attribut) True progressif Inferred relationship Some 2
Autosomal dominant limb-girdle muscular dystrophy type 1H évolution clinique (attribut) True progressif Inferred relationship Some 2
Spondyloepiphyseal dysplasia with congenital joint dislocations (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
dysplasie épiphysaire multiple évolution clinique (attribut) True progressif Inferred relationship Some 2
Distal myopathy with posterior leg and anterior hand involvement (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
Autosomal dominant muscular dystrophy with gene located at 5q31 évolution clinique (attribut) True progressif Inferred relationship Some 2
Progressive myoclonic epilepsy type 8 (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 1
Muscular dystrophy with predominantly proximal limb girdle distribution évolution clinique (attribut) True progressif Inferred relationship Some 2
X-linked muscular dystrophy with limb girdle distribution évolution clinique (attribut) True progressif Inferred relationship Some 2
X-linked muscular dystrophy with abnormal dystrophin évolution clinique (attribut) True progressif Inferred relationship Some 2
Intermediate X-linked muscular dystrophy évolution clinique (attribut) True progressif Inferred relationship Some 2
Larsen syndrome évolution clinique (attribut) True progressif Inferred relationship Some 5
Chondrodysplasia with joint dislocations gPAPP type (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
X-linked limb girdle muscular dystrophy with normal dystrophin évolution clinique (attribut) True progressif Inferred relationship Some 2
Ji muscular dystrophy évolution clinique (attribut) False progressif Inferred relationship Some 2
Autosomal recessive muscular dystrophy with limb girdle distribution évolution clinique (attribut) True progressif Inferred relationship Some 2
Autosomal recessive muscular dystrophy with abnormal dystrophin-associated glycoprotein évolution clinique (attribut) True progressif Inferred relationship Some 1
Severe autosomal recessive muscular dystrophy of childhood - North African type évolution clinique (attribut) False progressif Inferred relationship Some 3
Autosomal recessive muscular dystrophy with gene located at 15q évolution clinique (attribut) False progressif Inferred relationship Some 1
Langer mesomelic dysplasia syndrome évolution clinique (attribut) True progressif Inferred relationship Some 2
Autosomal dominant muscular dystrophy not predominantly limb girdle évolution clinique (attribut) True progressif Inferred relationship Some 2
Autosomal dominant limb girdle muscular dystrophy type 1A (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
Western type of congenital muscular dystrophy évolution clinique (attribut) True progressif Inferred relationship Some 2
Autosomal dominant limb girdle muscular dystrophy type 1C (disorder) évolution clinique (attribut) False progressif Inferred relationship Some 2
Congenital muscular dystrophy with arthrogryposis multiplex congenita évolution clinique (attribut) True progressif Inferred relationship Some 2
Autosomal dominant limb girdle muscular dystrophy type 1D (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
Autosomal dominant limb girdle muscular dystrophy type 1E (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
Eichsfeld type congenital muscular dystrophy évolution clinique (attribut) True progressif Inferred relationship Some 2
Autosomal dominant limb girdle muscular dystrophy type 1F (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
Hutterite type of muscular dystrophy évolution clinique (attribut) True progressif Inferred relationship Some 2
Congenital muscular dystrophy with intellectual disability évolution clinique (attribut) True progressif Inferred relationship Some 3
Autosomal dominant limb girdle muscular dystrophy type 1G (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
Adult onset autosomal recessive muscular dystrophy with normal dystrophin évolution clinique (attribut) True progressif Inferred relationship Some 2

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