FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

389167007: Acromesomelic dysplasia Hunter-Thompson type (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2003. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1483219011 Hunter-Thompson dysplasia en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
4591525019 Acromesomelic dysplasia Hunter-Thompson type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4591527010 Acromesomelic dysplasia Hunter-Thompson type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1463346010 Hunter-Thompson dysplasia (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1463346010 Hunter-Thompson dysplasia (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
1483219011 Hunter-Thompson dysplasia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1483219011 Hunter-Thompson dysplasia en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
4591525019 Acromesomelic dysplasia Hunter-Thompson type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4591527010 Acromesomelic dysplasia Hunter-Thompson type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3429321001000115 Dysplasie, akromesomele, Typ Hunter-Thompson de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5246681000241117 nanisme acromésomélique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5246681000241117 nanisme acromésomélique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3429321001000115 Dysplasie, akromesomele, Typ Hunter-Thompson de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Acromesomelic dysplasia Hunter-Thompson type (disorder) Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Acromesomelic dysplasia Hunter-Thompson type (disorder) Is a Acromesomelic dysplasia group (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Acromesomelic dysplasia Hunter-Thompson type (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Acromesomelic dysplasia Hunter-Thompson type (disorder) Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Acromesomelic dysplasia Hunter-Thompson type (disorder) Finding site Musculoskeletal structure of limb (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Acromesomelic dysplasia Hunter-Thompson type (disorder) Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Acromesomelic dysplasia Hunter-Thompson type (disorder) Finding site Bone structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Acromesomelic dysplasia Hunter-Thompson type (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Acromesomelic dysplasia Hunter-Thompson type (disorder) Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Acromesomelic dysplasia Hunter-Thompson type (disorder) Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 2
Acromesomelic dysplasia Hunter-Thompson type (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Acromesomelic dysplasia Hunter-Thompson type (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Acromesomelic dysplasia Hunter-Thompson type (disorder) Associated morphology Dysplasia true Inferred relationship Existential restriction modifier (core metadata concept) 1
Acromesomelic dysplasia Hunter-Thompson type (disorder) Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Acromesomelic dysplasia Hunter-Thompson type (disorder) Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier (core metadata concept)
Acromesomelic dysplasia Hunter-Thompson type (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start