FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.21  |  FHIR Version n/a  User: [n/a]

763885008: Spondyloepimetaphyseal dysplasia Handigodu type (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
3645133013 Spondyloepimetaphyseal dysplasia Handigodu type en Synonym Active Only initial character case insensitive SNOMED CT core module
3645134019 Spondyloepimetaphyseal dysplasia Handigodu type (disorder) en Fully specified name 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 Handigodu type Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Spondyloepimetaphyseal dysplasia Handigodu type Is a Spondyloepimetaphyseal disorder true Inferred relationship Existential restriction modifier
Spondyloepimetaphyseal dysplasia Handigodu type Is a Connective tissue hereditary disorder false Inferred relationship Existential restriction modifier
Spondyloepimetaphyseal dysplasia Handigodu type Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier
Spondyloepimetaphyseal dysplasia Handigodu type Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 1
Spondyloepimetaphyseal dysplasia Handigodu type Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Spondyloepimetaphyseal dysplasia Handigodu type Finding site Bone structure true Inferred relationship Existential restriction modifier 1
Spondyloepimetaphyseal dysplasia Handigodu type Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Spondyloepimetaphyseal dysplasia Handigodu type Associated morphology Dysplasia true Inferred relationship Existential restriction modifier 1
Spondyloepimetaphyseal dysplasia Handigodu type Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Spondyloepimetaphyseal dysplasia Handigodu 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

Back to Start