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715672007: Multiple epiphyseal dysplasia type 4 (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
3303372011 Multiple epiphyseal dysplasia type 4 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3303373018 Multiple epiphyseal dysplasia type 4 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3303374012 Autosomal recessive multiple epiphyseal dysplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5401033013 Multiple epiphyseal dysplasia type 4 is a multiple epiphyseal dysplasia with a late-childhood onset, characterized by joint pain involving hips, knees, wrists, and fingers with occasional limitation of joint movements, deformity of hands, feet, and knees (club foot, clinodactyly, brachydactyly), scoliosis and slightly reduced adult height. Radiographs display flat epiphyses with early arthritis of the hip, and double-layered patella. Multiple epiphyseal dysplasia type 4 follows an autosomal recessive mode of transmission. The disease is allelic to diastrophic dwarfism, atelosteogenesis type 2 and achondrogenesis type 1B with whom it forms a clinical continuum. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401034019 Multiple epiphyseal dysplasia type 4 is a multiple epiphyseal dysplasia with a late-childhood onset, characterised by joint pain involving hips, knees, wrists, and fingers with occasional limitation of joint movements, deformity of hands, feet, and knees (club foot, clinodactyly, brachydactyly), scoliosis and slightly reduced adult height. Radiographs display flat epiphyses with early arthritis of the hip, and double-layered patella. Multiple epiphyseal dysplasia type 4 follows an autosomal recessive mode of transmission. The disease is allelic to diastrophic dwarfism, atelosteogenesis type 2 and achondrogenesis type 1B with whom it forms a clinical continuum. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3303372011 Multiple epiphyseal dysplasia type 4 (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3303372011 Multiple epiphyseal dysplasia type 4 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3303373018 Multiple epiphyseal dysplasia type 4 en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3303373018 Multiple epiphyseal dysplasia type 4 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3303374012 Autosomal recessive multiple epiphyseal dysplasia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3303374012 Autosomal recessive multiple epiphyseal dysplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3303375013 A multiple epiphyseal dysplasia with a late-childhood onset manifesting as joint pain involving hips, knees, wrists and fingers with occasional limitation of joint movements, deformity of hands, feet, and knees, scoliosis and slightly reduced adult height. Follows an autosomal recessive mode of transmission en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401033013 Multiple epiphyseal dysplasia type 4 is a multiple epiphyseal dysplasia with a late-childhood onset, characterized by joint pain involving hips, knees, wrists, and fingers with occasional limitation of joint movements, deformity of hands, feet, and knees (club foot, clinodactyly, brachydactyly), scoliosis and slightly reduced adult height. Radiographs display flat epiphyses with early arthritis of the hip, and double-layered patella. Multiple epiphyseal dysplasia type 4 follows an autosomal recessive mode of transmission. The disease is allelic to diastrophic dwarfism, atelosteogenesis type 2 and achondrogenesis type 1B with whom it forms a clinical continuum. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401034019 Multiple epiphyseal dysplasia type 4 is a multiple epiphyseal dysplasia with a late-childhood onset, characterised by joint pain involving hips, knees, wrists, and fingers with occasional limitation of joint movements, deformity of hands, feet, and knees (club foot, clinodactyly, brachydactyly), scoliosis and slightly reduced adult height. Radiographs display flat epiphyses with early arthritis of the hip, and double-layered patella. Multiple epiphyseal dysplasia type 4 follows an autosomal recessive mode of transmission. The disease is allelic to diastrophic dwarfism, atelosteogenesis type 2 and achondrogenesis type 1B with whom it forms a clinical continuum. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3432811001000110 Dysplasie, epiphysäre multiple, Typ 4 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
926331000172119 dysplasie épiphysaire multiple type 4 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
932941000172114 dysplasie polyépiphysaire autosomique récessive fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
926331000172119 dysplasie épiphysaire multiple type 4 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
932941000172114 dysplasie polyépiphysaire autosomique récessive fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3432811001000110 Dysplasie, epiphysäre multiple, Typ 4 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 4 (disorder) Is a Multiple epiphyseal dysplasia true Inferred relationship Existential restriction modifier (core metadata concept)
Multiple epiphyseal dysplasia type 4 (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Multiple epiphyseal dysplasia type 4 (disorder) Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 3
Multiple epiphyseal dysplasia type 4 (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
Multiple epiphyseal dysplasia type 4 (disorder) Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
Multiple epiphyseal dysplasia type 4 (disorder) Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 4
Multiple epiphyseal dysplasia type 4 (disorder) Finding site Structure of epiphysis false Inferred relationship Existential restriction modifier (core metadata concept) 4
Multiple epiphyseal dysplasia type 4 (disorder) Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Multiple epiphyseal dysplasia type 4 (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Multiple epiphyseal dysplasia type 4 (disorder) Finding site Structure of epiphysis true Inferred relationship Existential restriction modifier (core metadata concept) 1
Multiple epiphyseal dysplasia type 4 (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Multiple epiphyseal dysplasia type 4 (disorder) Associated morphology Dysplasia true Inferred relationship Existential restriction modifier (core metadata concept) 1
Multiple epiphyseal dysplasia type 4 (disorder) Clinical course Progressive true Inferred relationship Existential restriction modifier (core metadata concept) 2
Multiple epiphyseal dysplasia type 4 (disorder) 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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