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770603000: X-linked spondyloepimetaphyseal dysplasia (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3701524011 X-linked spondyloepimetaphyseal dysplasia (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
3701525012 X-linked spondyloepimetaphyseal dysplasia en Synonym Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
X-linked spondyloepimetaphyseal dysplasia Is a X-linked hereditary disease false Inferred relationship Existential restriction modifier
X-linked spondyloepimetaphyseal dysplasia Occurrence Congenital true Inferred relationship Existential restriction modifier 1
X-linked spondyloepimetaphyseal dysplasia Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 1
X-linked spondyloepimetaphyseal dysplasia Finding site Bone structure true Inferred relationship Existential restriction modifier 1
X-linked spondyloepimetaphyseal dysplasia Is a Spondyloepimetaphyseal disorder true Inferred relationship Existential restriction modifier
X-linked spondyloepimetaphyseal dysplasia Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier
X-linked spondyloepimetaphyseal dysplasia Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
X-linked spondyloepimetaphyseal dysplasia Associated morphology Dysplasia true Inferred relationship Existential restriction modifier 1
X-linked spondyloepimetaphyseal dysplasia Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
X-linked spondyloepimetaphyseal dysplasia Interprets Height / growth measure true Inferred relationship Existential restriction modifier 2
X-linked spondyloepimetaphyseal dysplasia Is a X-linked recessive hereditary disease 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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