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

1003862001: Rhizomelic chondrodysplasia punctata type 1 (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4166843010 Rhizomelic chondrodysplasia punctata type 1 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4166844016 Rhizomelic chondrodysplasia punctata type 1 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4166843010 Rhizomelic chondrodysplasia punctata type 1 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4166844016 Rhizomelic chondrodysplasia punctata type 1 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5601241000241111 chondrodysplasie ponctuée rhizomélique de type 1 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5601241000241111 chondrodysplasie ponctuée rhizomélique de type 1 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Rhizomelic chondrodysplasia punctata type 1 (disorder) Is a Rhizomelic chondrodysplasia punctata syndrome true Inferred relationship Existential restriction modifier (core metadata concept)
Rhizomelic chondrodysplasia punctata type 1 (disorder) Associated morphology Dysplasia true Inferred relationship Existential restriction modifier (core metadata concept) 1
Rhizomelic chondrodysplasia punctata type 1 (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Rhizomelic chondrodysplasia punctata type 1 (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Rhizomelic chondrodysplasia punctata type 1 (disorder) Finding site Bone structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Rhizomelic chondrodysplasia punctata type 1 (disorder) Finding site Structure of epiphysis true Inferred relationship Existential restriction modifier (core metadata concept) 2
Rhizomelic chondrodysplasia punctata type 1 (disorder) Associated morphology Deformity (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Rhizomelic chondrodysplasia punctata type 1 (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Rhizomelic chondrodysplasia punctata type 1 (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start