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715673002: Multiple epiphyseal dysplasia type 1 (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3303376014 Multiple epiphyseal dysplasia type 1 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3303377017 Multiple epiphyseal dysplasia type 1 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3303378010 Polyepiphyseal dysplasia type 1 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5401035018 Multiple epiphyseal dysplasia type 1 (MED 1) is a form of multiple epiphyseal dysplasia that is characterized by normal or mild short stature, pain in the hips and/or knees, progressive deformity of extremities and early-onset osteoarthrosis. Specific features to MED 1 include a more pronounced involvement of hip joints and gait abnormality and a shorter adult height. MED1 is allelic to pseudoachondroplasia with which it shares clinical and radiological features. The disease follows an autosomal dominant mode of transmission. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401036017 Multiple epiphyseal dysplasia type 1 (MED 1) is a form of multiple epiphyseal dysplasia that is characterised by normal or mild short stature, pain in the hips and/or knees, progressive deformity of extremities and early-onset osteoarthrosis. Specific features to MED 1 include a more pronounced involvement of hip joints and gait abnormality and a shorter adult height. MED1 is allelic to pseudoachondroplasia with which it shares clinical and radiological features. The disease follows an autosomal dominant mode of transmission. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3303376014 Multiple epiphyseal dysplasia type 1 (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3303376014 Multiple epiphyseal dysplasia type 1 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3303377017 Multiple epiphyseal dysplasia type 1 en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3303377017 Multiple epiphyseal dysplasia type 1 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3303378010 Polyepiphyseal dysplasia type 1 en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3303378010 Polyepiphyseal dysplasia type 1 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3303379019 A form of multiple epiphyseal dysplasia manifesting as normal or mild short stature, pain in the hips and/or knees, progressive deformity of extremities and early onset osteoarthrosis. Specific features include a more pronounced involvement of hip joints and gait abnormality and a shorter adult height. The disease follows an autosomal dominant mode of transmission. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401035018 Multiple epiphyseal dysplasia type 1 (MED 1) is a form of multiple epiphyseal dysplasia that is characterized by normal or mild short stature, pain in the hips and/or knees, progressive deformity of extremities and early-onset osteoarthrosis. Specific features to MED 1 include a more pronounced involvement of hip joints and gait abnormality and a shorter adult height. MED1 is allelic to pseudoachondroplasia with which it shares clinical and radiological features. The disease follows an autosomal dominant mode of transmission. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401036017 Multiple epiphyseal dysplasia type 1 (MED 1) is a form of multiple epiphyseal dysplasia that is characterised by normal or mild short stature, pain in the hips and/or knees, progressive deformity of extremities and early-onset osteoarthrosis. Specific features to MED 1 include a more pronounced involvement of hip joints and gait abnormality and a shorter adult height. MED1 is allelic to pseudoachondroplasia with which it shares clinical and radiological features. The disease follows an autosomal dominant mode of transmission. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3411021001000110 Dysplasie, epiphysäre multiple, Typ 1 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
943401000172112 dysplasie polyépiphysaire type 1 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
1000891000172112 dysplasie épiphysaire multiple type 1 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
943401000172112 dysplasie polyépiphysaire type 1 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
1000891000172112 dysplasie épiphysaire multiple type 1 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3411021001000110 Dysplasie, epiphysäre multiple, Typ 1 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Multiple epiphyseal dysplasia type 1 Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Multiple epiphyseal dysplasia type 1 Is a Multiple epiphyseal dysplasia true Inferred relationship Existential restriction modifier (core metadata concept)
Multiple epiphyseal dysplasia type 1 Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 3
Multiple epiphyseal dysplasia type 1 Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
Multiple epiphyseal dysplasia type 1 Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
Multiple epiphyseal dysplasia type 1 Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 4
Multiple epiphyseal dysplasia type 1 Finding site Structure of epiphysis false Inferred relationship Existential restriction modifier (core metadata concept) 4
Multiple epiphyseal dysplasia type 1 Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Multiple epiphyseal dysplasia type 1 Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Multiple epiphyseal dysplasia type 1 Finding site Structure of epiphysis true Inferred relationship Existential restriction modifier (core metadata concept) 1
Multiple epiphyseal dysplasia type 1 Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Multiple epiphyseal dysplasia type 1 Associated morphology Dysplasia true Inferred relationship Existential restriction modifier (core metadata concept) 1
Multiple epiphyseal dysplasia type 1 Clinical course Progressive true Inferred relationship Existential restriction modifier (core metadata concept) 2
Multiple epiphyseal dysplasia type 1 Interprets Height / growth measure (observable entity) true Inferred relationship Existential restriction modifier (core metadata concept) 3

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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