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782821004: Spondyloepimetaphyseal dysplasia Isidor type (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3756065013 Spondyloepimetaphyseal dysplasia Isidor type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3756066014 Spondyloepimetaphyseal dysplasia Isidor type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3756073016 A rare primary bone dysplasia disorder with characteristics of normal birth length with early postnatal growth deficiency resulting in severe disproportionate short stature (with short trunk and limbs), severe genu varum, flexion contractures in the hips and lumbar hyperlordosis. Radiological findings reveal platyspondyly with central indentation of vertebral endplates, progressive and severe epimetaphyseal abnormalities that primarily affect the lower limbs and include very small, irregular proximal femoral and knee epiphyses, severe coxa vara, delayed ossification of proximal femoral epiphyses and irregular distal femoral and proximal tibial metaphyses. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3756065013 Spondyloepimetaphyseal dysplasia Isidor type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3756066014 Spondyloepimetaphyseal dysplasia Isidor type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3756073016 A rare primary bone dysplasia disorder with characteristics of normal birth length with early postnatal growth deficiency resulting in severe disproportionate short stature (with short trunk and limbs), severe genu varum, flexion contractures in the hips and lumbar hyperlordosis. Radiological findings reveal platyspondyly with central indentation of vertebral endplates, progressive and severe epimetaphyseal abnormalities that primarily affect the lower limbs and include very small, irregular proximal femoral and knee epiphyses, severe coxa vara, delayed ossification of proximal femoral epiphyses and irregular distal femoral and proximal tibial metaphyses. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3451411001000116 Dysplasie, spondyloepimetaphysäre, Typ Isidor de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5590781000241112 dysplasie spondyloépimétaphysaire de type Isidor fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5590781000241112 dysplasie spondyloépimétaphysaire de type Isidor fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3451411001000116 Dysplasie, spondyloepimetaphysäre, Typ Isidor 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
Spondyloepimetaphyseal dysplasia Isidor type Associated morphology Dysplasia true Inferred relationship Existential restriction modifier (core metadata concept) 1
Spondyloepimetaphyseal dysplasia Isidor type Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Spondyloepimetaphyseal dysplasia Isidor type Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Spondyloepimetaphyseal dysplasia Isidor type Finding site Bone structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Spondyloepimetaphyseal dysplasia Isidor type Is a Spondyloepimetaphyseal disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Spondyloepimetaphyseal dysplasia Isidor type Interprets Height / growth measure (observable entity) true Inferred relationship Existential restriction modifier (core metadata concept) 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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