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1363114004: Multiple epiphyseal dysplasia type 7 (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Apr 2025. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5447251010 EDM7 - epiphyseal dysplasia multiple 7 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5447252015 Multiple epiphyseal dysplasia type 7 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5447253013 Multiple epiphyseal dysplasia type 7 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5447254019 CANT1-related multiple epiphyseal dysplasia en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5447255018 MED7 - multiple epiphyseal dysplasia type 7 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5447264011 A rare multiple epiphyseal dysplasia characterized by mild short stature, joint pain and early-onset osteoarthropathy, frequently requiring joint replacement. Radiographs from affected individuals may manifest features typical of Desbuquois dysplasia, including irregularly shaped capital femoral epiphyses, a short femoral neck (resembles the Swedish key appearance of the proximal femur) and advanced carpal ossification in the hands. However, some other features typical of Desbuquois dysplasia like joint dislocations, scoliosis, coronal clefts, or other hand anomalies including accessory ossification centers and/or delta phalanx are not observed. Anterior wedging of vertebral bodies, small epiphyses at the knees with metaphyseal flare may be present. Patients have normal metacarpal and phalangeal lengths, no distinctive facies nor neurologic complications. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5447265012 A rare multiple epiphyseal dysplasia characterised by mild short stature, joint pain and early-onset osteoarthropathy, frequently requiring joint replacement. Radiographs from affected individuals may manifest features typical of Desbuquois dysplasia, including irregularly shaped capital femoral epiphyses, a short femoral neck (resembles the Swedish key appearance of the proximal femur) and advanced carpal ossification in the hands. However, some other features typical of Desbuquois dysplasia like joint dislocations, scoliosis, coronal clefts, or other hand anomalies including accessory ossification centres and/or delta phalanx are not observed. Anterior wedging of vertebral bodies, small epiphyses at the knees with metaphyseal flare may be present. Patients have normal metacarpal and phalangeal lengths, no distinctive facies nor neurologic complications. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Multiple epiphyseal dysplasia type 7 (disorder) Is a Multiple epiphyseal dysplasia true Inferred relationship Some
Multiple epiphyseal dysplasia type 7 (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Multiple epiphyseal dysplasia type 7 (disorder) Clinical course Progressive (qualifier value) true Inferred relationship Some 2
Multiple epiphyseal dysplasia type 7 (disorder) Interprets Height / growth measure false Inferred relationship Some 3
Multiple epiphyseal dysplasia type 7 (disorder) Occurrence Congenital true Inferred relationship Some 1
Multiple epiphyseal dysplasia type 7 (disorder) Finding site Structure of epiphysis true Inferred relationship Some 1
Multiple epiphyseal dysplasia type 7 (disorder) Associated morphology Dysplasia true Inferred relationship Some 1
Multiple epiphyseal dysplasia type 7 (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Multiple epiphyseal dysplasia type 7 (disorder) Interprets Body height (observable entity) true Inferred relationship Some 3
Multiple epiphyseal dysplasia type 7 (disorder) Has interpretation Below reference range true Inferred relationship Some 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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