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768935003: Multiple epiphyseal dysplasia Lowry type (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). 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 Only initial character case insensitive (core metadata concept) SNOMED CT core
3687541015 Multiple epiphyseal dysplasia Lowry type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3687542010 Multiple epiphyseal dysplasia with Robin phenotype en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5404758010 Multiple epiphyseal dysplasia, Lowry type is a rare primary bone dysplasia characterized by 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 Entire term case sensitive (core metadata concept) SNOMED CT core
5404759019 Multiple epiphyseal dysplasia, Lowry type is a rare primary bone dysplasia characterised by 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 Entire term case sensitive (core metadata concept) SNOMED CT core
3687540019 Multiple epiphyseal dysplasia Lowry type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3687541015 Multiple epiphyseal dysplasia Lowry type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3687542010 Multiple epiphyseal dysplasia with Robin phenotype en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) 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 Entire term case sensitive (core metadata concept) SNOMED CT core
5404758010 Multiple epiphyseal dysplasia, Lowry type is a rare primary bone dysplasia characterized by 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 Entire term case sensitive (core metadata concept) SNOMED CT core
5404759019 Multiple epiphyseal dysplasia, Lowry type is a rare primary bone dysplasia characterised by 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 Entire term case sensitive (core metadata concept) SNOMED CT core
3448781001000110 Dysplasie, epiphysäre multiple, Typ Lowry de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
996561000172112 dysplasie épiphysaire multiple type Lowry fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
1010531000172112 dysplasie épiphysaire multiple avec phénotype de Robin fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
996561000172112 dysplasie épiphysaire multiple type Lowry fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
1010531000172112 dysplasie épiphysaire multiple avec phénotype de Robin fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3448781001000110 Dysplasie, epiphysäre multiple, Typ Lowry 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 Lowry type Is a Multiple epiphyseal dysplasia true Inferred relationship Existential restriction modifier (core metadata concept)
Multiple epiphyseal dysplasia Lowry type Finding site Structure of epiphysis true Inferred relationship Existential restriction modifier (core metadata concept) 1
Multiple epiphyseal dysplasia Lowry type Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Multiple epiphyseal dysplasia Lowry type Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Multiple epiphyseal dysplasia Lowry type Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Multiple epiphyseal dysplasia Lowry type Associated morphology Dysplasia true Inferred relationship Existential restriction modifier (core metadata concept) 1
Multiple epiphyseal dysplasia Lowry type Clinical course Progressive true Inferred relationship Existential restriction modifier (core metadata concept) 2
Multiple epiphyseal dysplasia Lowry type Interprets Height / growth measure (observable entity) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Multiple epiphyseal dysplasia Lowry type Is a Rhizomelic dysplasia (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Multiple epiphyseal dysplasia Lowry type Interprets Limb length true Inferred relationship Existential restriction modifier (core metadata concept) 5
Multiple epiphyseal dysplasia Lowry type Has interpretation Below reference range true Inferred relationship Existential restriction modifier (core metadata concept) 5
Multiple epiphyseal dysplasia Lowry type Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 4
Multiple epiphyseal dysplasia Lowry type Finding site Bone structure of extremity true Inferred relationship Existential restriction modifier (core metadata concept) 4
Multiple epiphyseal dysplasia Lowry type Associated morphology Dysplasia true Inferred relationship Existential restriction modifier (core metadata concept) 4
Multiple epiphyseal dysplasia Lowry type Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 4
Multiple epiphyseal dysplasia Lowry type Is a Multiple malformation syndrome with facial-limb defects as major feature true Inferred relationship Existential restriction modifier (core metadata concept)
Multiple epiphyseal dysplasia Lowry type Has interpretation Below reference range true Inferred relationship Existential restriction modifier (core metadata concept) 3
Multiple epiphyseal dysplasia Lowry type Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 6
Multiple epiphyseal dysplasia Lowry type Finding site Face structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 6
Multiple epiphyseal dysplasia Lowry type Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 6
Multiple epiphyseal dysplasia Lowry type Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 6

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

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

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