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766820007: Spondyloepimetaphyseal dysplasia with multiple dislocations (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2018. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3662733015 Spondyloepimetaphyseal dysplasia with multiple dislocations en Synonym Active Entire term case insensitive SNOMED CT core module
3662734014 Spondyloepimetaphyseal dysplasia with multiple dislocations (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3662735010 Spondyloepimetaphyseal dysplasia with joint laxity type 2 en Synonym Active Entire term case insensitive SNOMED CT core module
3662736011 Spondyloepimetaphyseal dysplasia with joint laxity leptodactylic type en Synonym Active Entire term case insensitive SNOMED CT core module
3662737019 Spondyloepimetaphyseal dysplasia with joint laxity Hall type en Synonym Active Only initial character case insensitive SNOMED CT core module
3662738012 Spondyloepimetaphyseal dysplasia with multiple dislocations Hall type en Synonym Active Only initial character case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Spondyloepimetaphyseal dysplasia with multiple dislocations Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier
Spondyloepimetaphyseal dysplasia with multiple dislocations Is a Multiple dislocations with dysplasia true Inferred relationship Existential restriction modifier
Spondyloepimetaphyseal dysplasia with multiple dislocations Finding site Bone structure true Inferred relationship Existential restriction modifier 1
Spondyloepimetaphyseal dysplasia with multiple dislocations Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 1
Spondyloepimetaphyseal dysplasia with multiple dislocations Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Spondyloepimetaphyseal dysplasia with multiple dislocations Is a Connective tissue hereditary disorder false Inferred relationship Existential restriction modifier
Spondyloepimetaphyseal dysplasia with multiple dislocations Is a Spondyloepimetaphyseal disorder true Inferred relationship Existential restriction modifier
Spondyloepimetaphyseal dysplasia with multiple dislocations Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Spondyloepimetaphyseal dysplasia with multiple dislocations Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Spondyloepimetaphyseal dysplasia with multiple dislocations Associated morphology Dysplasia true Inferred relationship Existential restriction modifier 1
Spondyloepimetaphyseal dysplasia with multiple dislocations Finding site Joint structure of multiple body sites true Inferred relationship Existential restriction modifier 2
Spondyloepimetaphyseal dysplasia with multiple dislocations Associated morphology Dislocation true Inferred relationship Existential restriction modifier 2
Spondyloepimetaphyseal dysplasia with multiple dislocations Clinical course Progressive true Inferred relationship Existential restriction modifier 3
Spondyloepimetaphyseal dysplasia with multiple dislocations Due to Spontaneous event true Inferred relationship Existential restriction modifier 4
Spondyloepimetaphyseal dysplasia with multiple dislocations Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Spondyloepimetaphyseal dysplasia with multiple dislocations Interprets Height / growth measure true Inferred relationship Existential restriction modifier 5
Spondyloepimetaphyseal dysplasia with multiple dislocations Associated morphology Damage false Inferred relationship Existential restriction modifier 6
Spondyloepimetaphyseal dysplasia with multiple dislocations Is a Bone injury true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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