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719837003: X-linked dominant chondrodysplasia Chassaing Lacombe 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
3318109015 X-linked dominant chondrodysplasia Chassaing Lacombe type (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
3318110013 X-linked dominant chondrodysplasia Chassaing Lacombe type 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 dominant chondrodysplasia Chassaing Lacombe type Is a X-linked hereditary disease false Inferred relationship Existential restriction modifier
X-linked dominant chondrodysplasia Chassaing Lacombe type Is a Chondrodysplasia true Inferred relationship Existential restriction modifier
X-linked dominant chondrodysplasia Chassaing Lacombe type Is a Connective tissue hereditary disorder false Inferred relationship Existential restriction modifier
X-linked dominant chondrodysplasia Chassaing Lacombe type Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier
X-linked dominant chondrodysplasia Chassaing Lacombe type Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 2
X-linked dominant chondrodysplasia Chassaing Lacombe type Occurrence Congenital false Inferred relationship Existential restriction modifier 2
X-linked dominant chondrodysplasia Chassaing Lacombe type Finding site Bone structure false Inferred relationship Existential restriction modifier 2
X-linked dominant chondrodysplasia Chassaing Lacombe type Finding site Bone structure true Inferred relationship Existential restriction modifier 1
X-linked dominant chondrodysplasia Chassaing Lacombe type Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
X-linked dominant chondrodysplasia Chassaing Lacombe type Occurrence Congenital true Inferred relationship Existential restriction modifier 1
X-linked dominant chondrodysplasia Chassaing Lacombe type Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 1
X-linked dominant chondrodysplasia Chassaing Lacombe type Associated morphology Dysplasia true Inferred relationship Existential restriction modifier 1
X-linked dominant chondrodysplasia Chassaing Lacombe type Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
X-linked dominant chondrodysplasia Chassaing Lacombe type Is a X-linked dominant 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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