FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

51952004: Spondyloepiphyseal dysplasia tarda (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
86484012 Spondyloepiphyseal dysplasia tarda en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
789908012 Spondyloepiphyseal dysplasia tarda (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1231062010 SEDT - Spondyloepiphyseal dysplasia tarda en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
86484012 Spondyloepiphyseal dysplasia tarda en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
86484012 Spondyloepiphyseal dysplasia tarda en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
86485013 X-linked spondyloepiphyseal dysplasia en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
789908012 Spondyloepiphyseal dysplasia tarda (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
789908012 Spondyloepiphyseal dysplasia tarda (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1231061015 X-linked spondyloepiphyseal dysplasia tarda en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1231061015 X-linked spondyloepiphyseal dysplasia tarda en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
1231062010 SEDT - Spondyloepiphyseal dysplasia tarda en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1231062010 SEDT - Spondyloepiphyseal dysplasia tarda en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3434451001000116 Dysplasie, spondyloepiphysäre verzögerte de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
909441000172117 dysplasie spondylo-épiphysaire tardive fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
909441000172117 dysplasie spondylo-épiphysaire tardive fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3434451001000116 Dysplasie, spondyloepiphysäre verzögerte de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


15 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Spondyloepiphyseal dysplasia tarda Is a Osteochondrodysplasia syndrome true Inferred relationship Existential restriction modifier (core metadata concept)
Spondyloepiphyseal dysplasia tarda Is a Spondyloepimetaphyseal disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Spondyloepiphyseal dysplasia tarda Associated morphology Dysplasia true Inferred relationship Existential restriction modifier (core metadata concept) 1
Spondyloepiphyseal dysplasia tarda Finding site Skeletal system structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Spondyloepiphyseal dysplasia tarda Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Spondyloepiphyseal dysplasia tarda Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Spondyloepiphyseal dysplasia tarda Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 2
Spondyloepiphyseal dysplasia tarda Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier (core metadata concept)
Spondyloepiphyseal dysplasia tarda Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Spondyloepiphyseal dysplasia tarda Finding site Bone structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Spondyloepiphyseal dysplasia tarda Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Spondyloepiphyseal dysplasia tarda Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Spondyloepiphyseal dysplasia tarda Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 2
Spondyloepiphyseal dysplasia tarda Is a Connective tissue hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Spondyloepiphyseal dysplasia tarda Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier (core metadata concept)
Spondyloepiphyseal dysplasia tarda Is a X-linked hereditary disease false Inferred relationship Existential restriction modifier (core metadata concept)
Spondyloepiphyseal dysplasia tarda Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Spondyloepiphyseal dysplasia tarda Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Spondyloepiphyseal dysplasia tarda Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Spondyloepiphyseal dysplasia tarda Interprets Height / growth measure (observable entity) true Inferred relationship Existential restriction modifier (core metadata concept) 2

Inbound Relationships Type Active Source Characteristic Refinability Group
Multiple epiphyseal dysplasia Is a True Spondyloepiphyseal dysplasia tarda Inferred relationship Existential restriction modifier (core metadata concept)
Spondyloepiphyseal dysplasia tarda Kohn type (disorder) Is a True Spondyloepiphyseal dysplasia tarda Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

Back to Start