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719201004: Spondyloepimetaphyseal dysplasia Shohat type (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3315399015 Spondyloepimetaphyseal dysplasia Shohat type (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
3315400010 Spondyloepimetaphyseal dysplasia Shohat 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 Shohat type Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Spondyloepimetaphyseal dysplasia Shohat type Is a Spondyloepimetaphyseal disorder true Inferred relationship Existential restriction modifier
Spondyloepimetaphyseal dysplasia Shohat type Is a Connective tissue hereditary disorder false Inferred relationship Existential restriction modifier
Spondyloepimetaphyseal dysplasia Shohat type Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier
Spondyloepimetaphyseal dysplasia Shohat type Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 2
Spondyloepimetaphyseal dysplasia Shohat type Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Spondyloepimetaphyseal dysplasia Shohat type Finding site Bone structure false Inferred relationship Existential restriction modifier 2
Spondyloepimetaphyseal dysplasia Shohat type Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Spondyloepimetaphyseal dysplasia Shohat type Finding site Bone structure true Inferred relationship Existential restriction modifier 1
Spondyloepimetaphyseal dysplasia Shohat type Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 1
Spondyloepimetaphyseal dysplasia Shohat type Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Spondyloepimetaphyseal dysplasia Shohat type Associated morphology Dysplasia true Inferred relationship Existential restriction modifier 1
Spondyloepimetaphyseal dysplasia Shohat type Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Spondyloepimetaphyseal dysplasia Shohat type Interprets Height / growth measure true Inferred relationship Existential restriction modifier 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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