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255314001: Progressive (qualifier value)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

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

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Progressive Is a Behavior descriptors true Inferred relationship Existential restriction modifier
Progressive Is a Chronic true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome Clinical course True Progressive Inferred relationship Existential restriction modifier 6
Brachydactyly, mesomelia, intellectual disability, heart defect syndrome Clinical course True Progressive Inferred relationship Existential restriction modifier 5
Osteochondrodysplasia with osteopetrosis Clinical course True Progressive Inferred relationship Existential restriction modifier 4
Osteopetrosis - intermediate type Clinical course True Progressive Inferred relationship Existential restriction modifier 3
Congenital muscular dystrophy with integrin alpha-7 deficiency Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Osteopetrosis with renal tubular acidosis Clinical course True Progressive Inferred relationship Existential restriction modifier 3
Atelosteogenesis/diastrophic dysplasia Clinical course False Progressive Inferred relationship Existential restriction modifier 4
Scapuloperoneal muscular dystrophy Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Progressive myoclonic epilepsy type 5 Clinical course True Progressive Inferred relationship Existential restriction modifier 1
Progressive myoclonic epilepsy type 3 Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Autosomal recessive limb girdle muscular dystrophy type 2T Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Congenital muscular dystrophy due to lamin A/C mutation Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Autosomal recessive limb girdle muscular dystrophy type 2E Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Atelosteogenesis type 1 Clinical course True Progressive Inferred relationship Existential restriction modifier 3
Atelosteogenesis type 3 Clinical course True Progressive Inferred relationship Existential restriction modifier 3
Epidermolysis bullosa simplex with muscular dystrophy Clinical course True Progressive Inferred relationship Existential restriction modifier 3
Spondyloepimetaphyseal dysplasia with multiple dislocations Clinical course True Progressive Inferred relationship Existential restriction modifier 3
Early onset myopathy with fatal cardiomyopathy Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Madelung's deformity Clinical course False Progressive Inferred relationship Existential restriction modifier 4
Hereditary progressive muscular dystrophy Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Dentin dysplasia with sclerotic bone syndrome Clinical course True Progressive Inferred relationship Existential restriction modifier 3
Carbohydrate sulfotransferase 3 related skeletal dysplasia Clinical course True Progressive Inferred relationship Existential restriction modifier 3
Craniometadiaphyseal dysplasia Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Facioscapulohumeral muscular dystrophy Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Congenital muscular dystrophy Paradas type Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Charcot-Marie-Tooth disease type 2P Clinical course True Progressive Inferred relationship Existential restriction modifier 3
Osteomesopycnosis Clinical course False Progressive Inferred relationship Existential restriction modifier 2
Multiple epiphyseal dysplasia Lowry type Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Mesomelic dysplasia Kantaputra type Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Rhizomelic syndrome Urbach type Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Juvenile onset Huntington's disease Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Autosomal dominant Charcot-Marie-Tooth disease type 2O Clinical course True Progressive Inferred relationship Existential restriction modifier 3
Benign autosomal dominant osteopetrosis Clinical course True Progressive Inferred relationship Existential restriction modifier 3
Lower motor neuron syndrome with late-adult onset Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Mesomelic dysplasia with cleft palate and camptodactyly syndrome Clinical course True Progressive Inferred relationship Existential restriction modifier 4
Mesomelic dysplasia of hypoplastic ulna and fibula type Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Coxoauricular syndrome Clinical course False Progressive Inferred relationship Existential restriction modifier 4
Manifesting female carrier of X-linked muscular dystrophy Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Osteopetrosis Clinical course True Progressive Inferred relationship Existential restriction modifier 3
Hereditary myopathy limited to females Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Peripheral neuropathy, myopathy, hoarseness, hearing loss syndrome Clinical course True Progressive Inferred relationship Existential restriction modifier 1
Adult-onset distal myopathy due to valosin containing protein mutation Clinical course True Progressive Inferred relationship Existential restriction modifier 3
Finnish upper limb onset distal myopathy Clinical course True Progressive Inferred relationship Existential restriction modifier 3
Distal nebulin myopathy Clinical course True Progressive Inferred relationship Existential restriction modifier 1
Congenital muscular dystrophy with intellectual disability and severe epilepsy Clinical course True Progressive Inferred relationship Existential restriction modifier 3
Reunion-Indiana Amish type muscular dystrophy Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Multiple epiphyseal dysplasia Beighton type Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Segmental progressive overgrowth syndrome with fibroadipose hyperplasia Clinical course True Progressive Inferred relationship Existential restriction modifier 3
Ullrich congenital muscular dystrophy Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Autosomal dominant limb-girdle muscular dystrophy type 1H Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Spondyloepiphyseal dysplasia with congenital joint dislocations Clinical course True Progressive Inferred relationship Existential restriction modifier 3
Multiple epiphyseal dysplasia Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Distal myopathy with posterior leg and anterior hand involvement Clinical course True Progressive Inferred relationship Existential restriction modifier 3
Autosomal dominant muscular dystrophy with gene located at 5q31 Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Progressive myoclonic epilepsy type 8 Clinical course True Progressive Inferred relationship Existential restriction modifier 1
Muscular dystrophy with predominantly proximal limb girdle distribution Clinical course True Progressive Inferred relationship Existential restriction modifier 2
X-linked muscular dystrophy with limb girdle distribution Clinical course True Progressive Inferred relationship Existential restriction modifier 2
X-linked muscular dystrophy with abnormal dystrophin Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Intermediate X-linked muscular dystrophy Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Larsen syndrome Clinical course True Progressive Inferred relationship Existential restriction modifier 5
Chondrodysplasia with joint dislocations gPAPP type Clinical course True Progressive Inferred relationship Existential restriction modifier 3
X-linked limb girdle muscular dystrophy with normal dystrophin Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Ji muscular dystrophy Clinical course False Progressive Inferred relationship Existential restriction modifier 2
Autosomal recessive muscular dystrophy with limb girdle distribution Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Autosomal recessive muscular dystrophy with abnormal dystrophin-associated glycoprotein Clinical course True Progressive Inferred relationship Existential restriction modifier 1
Severe autosomal recessive muscular dystrophy of childhood - North African type Clinical course False Progressive Inferred relationship Existential restriction modifier 3
Autosomal recessive muscular dystrophy with gene located at 15q Clinical course False Progressive Inferred relationship Existential restriction modifier 1
Langer mesomelic dysplasia syndrome Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Autosomal dominant muscular dystrophy not predominantly limb girdle Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Autosomal dominant limb girdle muscular dystrophy type 1A Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Western type of congenital muscular dystrophy Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Autosomal dominant limb girdle muscular dystrophy type 1C Clinical course False Progressive Inferred relationship Existential restriction modifier 2
Congenital muscular dystrophy with arthrogryposis multiplex congenita Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Autosomal dominant limb girdle muscular dystrophy type 1D Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Autosomal dominant limb girdle muscular dystrophy type 1E Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Eichsfeld type congenital muscular dystrophy Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Autosomal dominant limb girdle muscular dystrophy type 1F Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Hutterite type of muscular dystrophy Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Congenital muscular dystrophy with intellectual disability Clinical course True Progressive Inferred relationship Existential restriction modifier 3
Autosomal dominant limb girdle muscular dystrophy type 1G Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Adult onset autosomal recessive muscular dystrophy with normal dystrophin Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Autosomal recessive myogenic arthrogryposis multiplex congenita Clinical course True Progressive Inferred relationship Existential restriction modifier 4
Congenital muscular hypertrophy-cerebral syndrome Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Autosomal dominant muscular dystrophy with limb girdle distribution Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Familial dementia British type Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Kelch like family member 9 related early-onset distal myopathy Clinical course True Progressive Inferred relationship Existential restriction modifier 3
Late onset proximal muscular dystrophy with dysarthria Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Multiple epiphyseal dysplasia with miniepiphyses Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Cleidorhizomelic syndrome Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Muscular dystrophy not predominantly limb girdle in distribution Clinical course True Progressive Inferred relationship Existential restriction modifier 2
X-linked muscular dystrophy not predominantly limb girdle Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Mesomelic dysplasia Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Benign scapuloperoneal muscular dystrophy with cardiomyopathy Clinical course False Progressive Inferred relationship Existential restriction modifier 2
Osteopetrosis hypogammaglobulinemia syndrome Clinical course True Progressive Inferred relationship Existential restriction modifier 5
Distal anoctaminopathy Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Autosomal recessive limb girdle muscular dystrophy type 2G Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Late onset Huntington's disease Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Autosomal recessive muscular dystrophy not predominantly limb girdle Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Autosomal recessive limb girdle muscular dystrophy type 2K Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Scapulohumeral muscular dystrophy Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Benign scapuloperoneal muscular dystrophy Clinical course True Progressive Inferred relationship Existential restriction modifier 2

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