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205465004: Chondrodysplasia (disorder)

SNOMED CT Concept\constatation clinique\...

\Disease\affection d'un système corporel\maladie du système musculosquelettique (trouble)\Disorder of skeletal system\Skeletal dysplasia\Chondrodysplasia
\Disease\affection d'un système corporel\maladie du système musculosquelettique (trouble)\Disorder of skeletal system\Disorder of bone (disorder)\Disorder of bone development (disorder)\Congenital anomaly of skeletal bone\Chondrodysplasia
\Disease\affection d'un système corporel\maladie du système musculosquelettique (trouble)\Congenital anomaly of musculoskeletal system\Skeletal dysplasia\Chondrodysplasia
\Disease\affection d'un système corporel\maladie du système musculosquelettique (trouble)\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Chondrodysplasia
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of musculoskeletal system\Skeletal dysplasia\Chondrodysplasia
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Chondrodysplasia
\Disease\trouble du développement\Disorder of bone development (disorder)\Congenital anomaly of skeletal bone\Chondrodysplasia
\Disease\trouble du développement\Congenital malformation\Congenital anomaly of musculoskeletal system\Skeletal dysplasia\Chondrodysplasia
\Disease\trouble du développement\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Chondrodysplasia

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

315050019 Chondrodysplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

590835013 Chondrodysplasia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Chondrodysplasia	survenue (attribut)	congénital	true	Inferred relationship	Some	1
Chondrodysplasia	Pathological process (attribute)	Pathological developmental process	true	Inferred relationship	Some	1
Chondrodysplasia	est un(e) (attribut)	Congenital anomaly of skeletal bone	true	Inferred relationship	Some
Chondrodysplasia	morphologie associée (attribut)	Congenital dysplasia	false	Inferred relationship	Some	1
Chondrodysplasia	localisation d'une constatation (attribut)	structure osseuse	false	Inferred relationship	Some	1
Chondrodysplasia	morphologie associée (attribut)	Congenital dysplasia	false	Inferred relationship	Some	1
Chondrodysplasia	est un(e) (attribut)	Skeletal dysplasia	true	Inferred relationship	Some
Chondrodysplasia	survenue (attribut)	congénital	false	Inferred relationship	Some	2
Chondrodysplasia	localisation d'une constatation (attribut)	structure osseuse	false	Inferred relationship	Some	2
Chondrodysplasia	morphologie associée (attribut)	Congenital dysplasia	false	Inferred relationship	Some	2
Chondrodysplasia	survenue (attribut)	congénital	false	Inferred relationship	Some
Chondrodysplasia	localisation d'une constatation (attribut)	Skeletal system structure	false	Inferred relationship	Some	1
Chondrodysplasia	morphologie associée (attribut)	dysplasie	true	Inferred relationship	Some	1
Chondrodysplasia	localisation d'une constatation (attribut)	structure osseuse	true	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Chondrodysplasia with joint dislocations gPAPP type (disorder)	est un(e) (attribut)	True	Chondrodysplasia	Inferred relationship	Some
Fibrochondrogenesis	est un(e) (attribut)	True	Chondrodysplasia	Inferred relationship	Some
Achondroplasia	est un(e) (attribut)	True	Chondrodysplasia	Inferred relationship	Some
QRICH1-related intellectual disability, chondrodysplasia syndrome	est un(e) (attribut)	True	Chondrodysplasia	Inferred relationship	Some
Lethal chondrodysplasia with fragmented bone (disorder)	est un(e) (attribut)	True	Chondrodysplasia	Inferred relationship	Some
Lethal retarded ossification syndromes	est un(e) (attribut)	True	Chondrodysplasia	Inferred relationship	Some
Multiple exostosis syndromes	est un(e) (attribut)	False	Chondrodysplasia	Inferred relationship	Some
Chondrodysplasia, unspecified	est un(e) (attribut)	False	Chondrodysplasia	Inferred relationship	Some
Dyschondroplasia NOS	est un(e) (attribut)	False	Chondrodysplasia	Inferred relationship	Some
Brachydactylous dwarfism Mseleni type	est un(e) (attribut)	True	Chondrodysplasia	Inferred relationship	Some
Lethal recessive chondrodysplasia (disorder)	est un(e) (attribut)	True	Chondrodysplasia	Inferred relationship	Some
chondrodysplasie dominante liée à l'X type Chassaing-Lacombe	est un(e) (attribut)	True	Chondrodysplasia	Inferred relationship	Some
Camptodactyly with fibrous tissue hyperplasia and skeletal dysplasia syndrome (disorder)	est un(e) (attribut)	True	Chondrodysplasia	Inferred relationship	Some
Chondrodysplasia with disorder of sex development syndrome (disorder)	est un(e) (attribut)	True	Chondrodysplasia	Inferred relationship	Some
Bone dysplasia lethal Holmgren type (disorder)	est un(e) (attribut)	True	Chondrodysplasia	Inferred relationship	Some

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
315050019	Chondrodysplasia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
590835013	Chondrodysplasia (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core