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768935003: Multiple epiphyseal dysplasia Lowry type (disorder)


Status: current, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3687540019 Multiple epiphyseal dysplasia Lowry type (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core
3687541015 Multiple epiphyseal dysplasia Lowry type en Synonym Active Initial character case insensitive SNOMED CT core
3687542010 Multiple epiphyseal dysplasia with Robin phenotype en Synonym Active Initial character case insensitive SNOMED CT core
3687543017 A rare primary bone dysplasia with characteristics of small, flat epiphyses (especially the capital femoral epiphyses), rhizomelic shortening of limbs, cleft of secondary palate, micrognathia, mild joint contractures and facial dysmorphism (including mildly upward-slanting palpebral fissures, hypertelorism, broad nasal tip). Additionally reported features include scoliosis, genu valgum, mild pectus excavatum, platyspondyly, dislocated radial heads, brachydactyly, hypoplastic fibulae and talipes equinovarus. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Multiple epiphyseal dysplasia Lowry type Pathological process Pathological developmental process true Inferred relationship Some 1
Multiple epiphyseal dysplasia Lowry type Associated morphology Dysplasia true Inferred relationship Some 1
Multiple epiphyseal dysplasia Lowry type Clinical course Progressive true Inferred relationship Some 2
Multiple epiphyseal dysplasia Lowry type Interprets Height / growth measure true Inferred relationship Some 3
Multiple epiphyseal dysplasia Lowry type Is a Multiple epiphyseal dysplasia true Inferred relationship Some
Multiple epiphyseal dysplasia Lowry type Finding site Structure of epiphysis true Inferred relationship Some 1
Multiple epiphyseal dysplasia Lowry type Associated morphology Congenital dysplasia false Inferred relationship Some 1
Multiple epiphyseal dysplasia Lowry type Occurrence Congenital true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Musculoskeletal finding reference set

Problem/Diagnosis reference set

Description inactivation indicator reference set

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