255314001: Progressive (qualifier value)

SNOMED CT Concept\Qualifier value\...

\Special atomic mapping values\Special disorder atoms\Courses\Chronic\Progressive (qualifier value)

\Descriptor (qualifier value)\Time patterns\Courses\Chronic\Progressive (qualifier value)
\Descriptor (qualifier value)\Behaviour descriptors\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:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Progressive (qualifier value)	Is a	Behaviour descriptors	true	Inferred relationship	Some
Progressive (qualifier value)	Is a	Chronic	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	6
Brachydactyly, mesomelia, intellectual disability, heart defect syndrome (disorder)	Clinical course	False	Progressive (qualifier value)	Inferred relationship	Some	5
Osteochondrodysplasia with osteopetrosis (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	4
Osteopetrosis - intermediate type	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Congenital muscular dystrophy with integrin alpha-7 deficiency (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Osteopetrosis with renal tubular acidosis	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Atelosteogenesis/diastrophic dysplasia	Clinical course	False	Progressive (qualifier value)	Inferred relationship	Some	4
Scapuloperoneal muscular dystrophy (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Progressive myoclonic epilepsy type 5 (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	1
Progressive myoclonic epilepsy type 3	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Autosomal recessive limb girdle muscular dystrophy type 2T (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Congenital muscular dystrophy due to lamin A/C mutation (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Autosomal recessive limb girdle muscular dystrophy type 2E (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Atelosteogenesis type 1 (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Atelosteogenesis type 3 (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Epidermolysis bullosa simplex with muscular dystrophy (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Spondyloepimetaphyseal dysplasia with multiple dislocations	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Early onset myopathy with fatal cardiomyopathy (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Madelung's deformity	Clinical course	False	Progressive (qualifier value)	Inferred relationship	Some	4
Hereditary progressive muscular dystrophy	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Dentin dysplasia with sclerotic bone syndrome	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Carbohydrate sulfotransferase 3 related skeletal dysplasia (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Craniometadiaphyseal dysplasia	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Facioscapulohumeral muscular dystrophy (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Congenital muscular dystrophy Paradas type (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Charcot-Marie-Tooth disease type 2P (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Osteomesopycnosis	Clinical course	False	Progressive (qualifier value)	Inferred relationship	Some	2
Multiple epiphyseal dysplasia Lowry type (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Mesomelic dysplasia Kantaputra type (disorder)	Clinical course	False	Progressive (qualifier value)	Inferred relationship	Some	2
Rhizomelic syndrome Urbach type	Clinical course	False	Progressive (qualifier value)	Inferred relationship	Some	2
Juvenile onset Huntington's disease	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Autosomal dominant Charcot-Marie-Tooth disease type 2O	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
ostéopétrose autosomique dominante bénigne	Clinical course	False	Progressive (qualifier value)	Inferred relationship	Some	3
Lower motor neuron syndrome with late-adult onset (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Mesomelic dysplasia with cleft palate and camptodactyly syndrome (disorder)	Clinical course	False	Progressive (qualifier value)	Inferred relationship	Some	4
Mesomelic dysplasia of hypoplastic ulna and fibula type (disorder)	Clinical course	False	Progressive (qualifier value)	Inferred relationship	Some	2
Coxoauricular syndrome (disorder)	Clinical course	False	Progressive (qualifier value)	Inferred relationship	Some	4
Manifesting female carrier of X-linked muscular dystrophy	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Osteopetrosis	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Hereditary myopathy limited to females	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Peripheral neuropathy, myopathy, hoarseness, hearing loss syndrome	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	1
Adult-onset distal myopathy due to valosin containing protein mutation (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Finnish upper limb onset distal myopathy	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Distal nebulin myopathy	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	1
Congenital muscular dystrophy with intellectual disability and severe epilepsy	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Reunion-Indiana Amish type muscular dystrophy	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Multiple epiphyseal dysplasia Beighton type (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Segmental progressive overgrowth syndrome with fibroadipose hyperplasia	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Ullrich congenital muscular dystrophy	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Autosomal dominant limb-girdle muscular dystrophy type 1H	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Spondyloepiphyseal dysplasia with congenital joint dislocations (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Multiple epiphyseal dysplasia	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Distal myopathy with posterior leg and anterior hand involvement (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Autosomal dominant muscular dystrophy with gene located at 5q31	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Progressive myoclonic epilepsy type 8 (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	1
Muscular dystrophy with predominantly proximal limb girdle distribution	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
X-linked muscular dystrophy with limb girdle distribution	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
X-linked muscular dystrophy with abnormal dystrophin	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Intermediate X-linked muscular dystrophy	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Larsen syndrome	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	5
Chondrodysplasia with joint dislocations gPAPP type (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
X-linked limb girdle muscular dystrophy with normal dystrophin	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Ji muscular dystrophy	Clinical course	False	Progressive (qualifier value)	Inferred relationship	Some	2
Autosomal recessive muscular dystrophy with limb girdle distribution	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Autosomal recessive muscular dystrophy with abnormal dystrophin-associated glycoprotein	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	1
Severe autosomal recessive muscular dystrophy of childhood - North African type	Clinical course	False	Progressive (qualifier value)	Inferred relationship	Some	3
Autosomal recessive muscular dystrophy with gene located at 15q	Clinical course	False	Progressive (qualifier value)	Inferred relationship	Some	1
Langer mesomelic dysplasia syndrome	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Autosomal dominant muscular dystrophy not predominantly limb girdle	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Autosomal dominant limb girdle muscular dystrophy type 1A (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Western type of congenital muscular dystrophy	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
dystrophie musculaire des ceintures autosomique dominante type 1C	Clinical course	False	Progressive (qualifier value)	Inferred relationship	Some	2
Congenital muscular dystrophy with arthrogryposis multiplex congenita	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Autosomal dominant limb girdle muscular dystrophy type 1D (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Autosomal dominant limb girdle muscular dystrophy type 1E (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Eichsfeld type congenital muscular dystrophy	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Autosomal dominant limb girdle muscular dystrophy type 1F (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Hutterite type of muscular dystrophy	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Congenital muscular dystrophy with intellectual disability	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Autosomal dominant limb girdle muscular dystrophy type 1G (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Adult onset autosomal recessive muscular dystrophy with normal dystrophin	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Autosomal recessive myogenic arthrogryposis multiplex congenita (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	4
Congenital muscular hypertrophy-cerebral syndrome	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Autosomal dominant muscular dystrophy with limb girdle distribution	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Familial dementia British type (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
KLHL9-related early-onset distal myopathy	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Late onset proximal muscular dystrophy with dysarthria	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Multiple epiphyseal dysplasia with miniepiphyses	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Cleidorhizomelic syndrome (disorder)	Clinical course	False	Progressive (qualifier value)	Inferred relationship	Some	2
Muscular dystrophy not predominantly limb girdle in distribution	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
X-linked muscular dystrophy not predominantly limb girdle	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Mesomelic dysplasia	Clinical course	False	Progressive (qualifier value)	Inferred relationship	Some	2
Benign scapuloperoneal muscular dystrophy with cardiomyopathy	Clinical course	False	Progressive (qualifier value)	Inferred relationship	Some	2
Osteopetrosis hypogammaglobulinemia syndrome (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	5
Distal anoctaminopathy	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Autosomal recessive limb girdle muscular dystrophy type 2G (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Late onset Huntington's disease	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Autosomal recessive muscular dystrophy not predominantly limb girdle	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Autosomal recessive limb girdle muscular dystrophy type 2K (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Scapulohumeral muscular dystrophy	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Benign scapuloperoneal muscular dystrophy	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2

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Id	Description	Lang	Type	Status	Case?	Module
380497019	Progressive	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
646336011	Progressive (qualifier value)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
7173101000172117	voortschrijdend	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)
7173111000172119	progressief	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)