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255314001: Progressive (qualifier value)

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
380497019 Progressive en Synonym Active Case insensitive SNOMED CT core
646336011 Progressive (qualifier value) en Fully specified name Active Case insensitive SNOMED CT core

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Progressive Is a Behaviour descriptors true Inferred relationship Some
Progressive Is a Chronic true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Steinert myotonic dystrophy syndrome Clinical course True Progressive Inferred relationship Some 2
Reunion Island Larsen-like syndrome Clinical course False Progressive Inferred relationship Some 4
Multiple epiphyseal dysplasia type 1 Clinical course True Progressive Inferred relationship Some 2
Diastrophic dysplasia Clinical course True Progressive Inferred relationship Some 3
Emery-Dreifuss muscular dystrophy Clinical course True Progressive Inferred relationship Some 2
Multiple epiphyseal dysplasia type 5 Clinical course True Progressive Inferred relationship Some 2
Multiple dislocations with dysplasia Clinical course True Progressive Inferred relationship Some 3
Menopausal muscular dystrophy syndrome Clinical course False Progressive Inferred relationship Some 2
Desbuquois syndrome Clinical course True Progressive Inferred relationship Some 3
Spondyloepimetaphyseal dysplasia with joint laxity Clinical course True Progressive Inferred relationship Some 3
Larsen-like osseous dysplasia, short stature syndrome Clinical course True Progressive Inferred relationship Some 3
Multiple epiphyseal dysplasia tarda type IIIa Clinical course True Progressive Inferred relationship Some 2
Progressive systemic sclerosis Clinical course True Progressive Inferred relationship Some 2
Distal myopathy 2 Clinical course True Progressive Inferred relationship Some 3
Eiken syndrome Clinical course True Progressive Inferred relationship Some 3
Ocular muscular dystrophy Clinical course False Progressive Inferred relationship Some 2
Parana hard skin syndrome Clinical course True Progressive Inferred relationship Some 1
Bethlem myopathy Clinical course True Progressive Inferred relationship Some 2
Dementia paralytica juvenilis Clinical course True Progressive Inferred relationship Some 3
Duchenne muscular dystrophy Clinical course True Progressive Inferred relationship Some 3
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome Clinical course True Progressive Inferred relationship Some 6
Brachydactyly, mesomelia, intellectual disability, heart defect syndrome Clinical course True Progressive Inferred relationship Some 5
Osteochondrodysplasia with osteopetrosis Clinical course True Progressive Inferred relationship Some 4
Osteopetrosis - intermediate type Clinical course True Progressive Inferred relationship Some 3
Congenital muscular dystrophy with integrin alpha-7 deficiency Clinical course True Progressive Inferred relationship Some 2
Osteopetrosis with renal tubular acidosis Clinical course True Progressive Inferred relationship Some 3
Atelosteogenesis/diastrophic dysplasia Clinical course False Progressive Inferred relationship Some 4
Scapuloperoneal muscular dystrophy Clinical course True Progressive Inferred relationship Some 2
Progressive myoclonic epilepsy type 5 Clinical course True Progressive Inferred relationship Some 1
Progressive myoclonic epilepsy type 3 Clinical course True Progressive Inferred relationship Some 2
Autosomal recessive limb girdle muscular dystrophy type 2T Clinical course True Progressive Inferred relationship Some 2
Congenital muscular dystrophy due to LMNA mutation Clinical course True Progressive Inferred relationship Some 2
Autosomal recessive limb girdle muscular dystrophy type 2E Clinical course True Progressive Inferred relationship Some 2
Atelosteogenesis type 1 Clinical course True Progressive Inferred relationship Some 3
Atelosteogenesis type 3 Clinical course True Progressive Inferred relationship Some 3
Epidermolysis bullosa simplex with muscular dystrophy Clinical course True Progressive Inferred relationship Some 3
Spondyloepimetaphyseal dysplasia with multiple dislocations Clinical course True Progressive Inferred relationship Some 3
Early onset myopathy with fatal cardiomyopathy Clinical course True Progressive Inferred relationship Some 2
Madelung's deformity Clinical course False Progressive Inferred relationship Some 4
Hereditary progressive muscular dystrophy Clinical course True Progressive Inferred relationship Some 2
Dentin dysplasia with sclerotic bone syndrome Clinical course True Progressive Inferred relationship Some 3
CHST3-related skeletal dysplasia Clinical course True Progressive Inferred relationship Some 3
Craniometadiaphyseal dysplasia Clinical course True Progressive Inferred relationship Some 2
Facioscapulohumeral muscular dystrophy Clinical course True Progressive Inferred relationship Some 2
Congenital myopathy Paradas type Clinical course True Progressive Inferred relationship Some 2
Charcot-Marie-Tooth disease type 2P Clinical course True Progressive Inferred relationship Some 3
Osteomesopycnosis Clinical course False Progressive Inferred relationship Some 2
Multiple epiphyseal dysplasia Lowry type Clinical course True Progressive Inferred relationship Some 2
Mesomelic dysplasia Kantaputra type Clinical course True Progressive Inferred relationship Some 2
Rhizomelic syndrome Urbach type Clinical course True Progressive Inferred relationship Some 2
Juvenile onset Huntington's disease Clinical course True Progressive Inferred relationship Some 2
Autosomal dominant Charcot-Marie-Tooth disease type 2O Clinical course True Progressive Inferred relationship Some 3
Benign autosomal dominant osteopetrosis Clinical course True Progressive Inferred relationship Some 3
Lower motor neuron syndrome with late-adult onset Clinical course True Progressive Inferred relationship Some 2
Reardon Hall Slaney syndrome Clinical course True Progressive Inferred relationship Some 4
Reinhardt Pfeiffer mesomelic dysplasia Clinical course True Progressive Inferred relationship Some 2
Coxoauricular syndrome Clinical course False Progressive Inferred relationship Some 4
Manifesting female carrier of X-linked muscular dystrophy Clinical course True Progressive Inferred relationship Some 2
Osteopetrosis Clinical course True Progressive Inferred relationship Some 3
Hereditary myopathy limited to females Clinical course True Progressive Inferred relationship Some 2
Peripheral neuropathy, myopathy, hoarseness, hearing loss syndrome Clinical course True Progressive Inferred relationship Some 1
Adult-onset distal myopathy due to valosin containing protein mutation Clinical course True Progressive Inferred relationship Some 3
Finnish upper limb onset distal myopathy Clinical course True Progressive Inferred relationship Some 3
Distal nebulin myopathy Clinical course True Progressive Inferred relationship Some 1
Congenital muscular dystrophy with intellectual disability and severe epilepsy Clinical course True Progressive Inferred relationship Some 3
Reunion-Indiana Amish type muscular dystrophy Clinical course True Progressive Inferred relationship Some 2
Multiple epiphyseal dysplasia Beighton type Clinical course True Progressive Inferred relationship Some 2
Segmental progressive overgrowth syndrome with fibroadipose hyperplasia Clinical course True Progressive Inferred relationship Some 3
Ullrich congenital muscular dystrophy Clinical course True Progressive Inferred relationship Some 2
Autosomal dominant limb-girdle muscular dystrophy type 1H Clinical course True Progressive Inferred relationship Some 2
Spondyloepiphyseal dysplasia with congenital joint dislocations Clinical course True Progressive Inferred relationship Some 3
Multiple epiphyseal dysplasia Clinical course True Progressive Inferred relationship Some 2
Distal myopathy with posterior leg and anterior hand involvement Clinical course True Progressive Inferred relationship Some 3
Autosomal dominant muscular dystrophy with gene located at 5q31 Clinical course True Progressive Inferred relationship Some 2
Progressive myoclonic epilepsy type 8 Clinical course True Progressive Inferred relationship Some 1
Muscular dystrophy with predominantly proximal limb girdle distribution Clinical course True Progressive Inferred relationship Some 2
X-linked muscular dystrophy with limb girdle distribution Clinical course True Progressive Inferred relationship Some 2
X-linked muscular dystrophy with abnormal dystrophin Clinical course True Progressive Inferred relationship Some 2
Intermediate X-linked muscular dystrophy Clinical course True Progressive Inferred relationship Some 2
Larsen syndrome Clinical course True Progressive Inferred relationship Some 5
Chondrodysplasia with joint dislocations gPAPP type Clinical course True Progressive Inferred relationship Some 3
X-linked limb girdle muscular dystrophy with normal dystrophin Clinical course True Progressive Inferred relationship Some 2
Ji muscular dystrophy Clinical course False Progressive Inferred relationship Some 2
Autosomal recessive muscular dystrophy with limb girdle distribution Clinical course True Progressive Inferred relationship Some 2
Autosomal recessive muscular dystrophy with abnormal dystrophin-associated glycoprotein Clinical course True Progressive Inferred relationship Some 1
Severe autosomal recessive muscular dystrophy of childhood - North African type Clinical course False Progressive Inferred relationship Some 3
Autosomal recessive muscular dystrophy with gene located at 15q Clinical course False Progressive Inferred relationship Some 1
Langer mesomelic dysplasia syndrome Clinical course True Progressive Inferred relationship Some 2
Autosomal dominant muscular dystrophy not predominantly limb girdle Clinical course True Progressive Inferred relationship Some 2
Autosomal dominant limb girdle muscular dystrophy type 1A Clinical course True Progressive Inferred relationship Some 2
Western type of congenital muscular dystrophy Clinical course True Progressive Inferred relationship Some 2
Autosomal dominant limb girdle muscular dystrophy type 1C Clinical course False Progressive Inferred relationship Some 2
Congenital muscular dystrophy with arthrogryposis multiplex congenita Clinical course True Progressive Inferred relationship Some 2
Autosomal dominant limb girdle muscular dystrophy type 1D Clinical course True Progressive Inferred relationship Some 2
Autosomal dominant limb girdle muscular dystrophy type 1E Clinical course True Progressive Inferred relationship Some 2
Eichsfeld type congenital muscular dystrophy Clinical course True Progressive Inferred relationship Some 2
Autosomal dominant limb girdle muscular dystrophy type 1F Clinical course True Progressive Inferred relationship Some 2
Hutterite type of muscular dystrophy Clinical course True Progressive Inferred relationship Some 2
Congenital muscular dystrophy with intellectual disability Clinical course True Progressive Inferred relationship Some 3
Autosomal dominant limb girdle muscular dystrophy type 1G Clinical course True Progressive Inferred relationship Some 2
Adult onset autosomal recessive muscular dystrophy with normal dystrophin Clinical course True Progressive Inferred relationship Some 2

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Reference Sets

Qualifier value foundation reference set

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