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205465004: Chondrodysplasia (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

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


16 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Chondrodysplasia Occurrence Congenital true Inferred relationship Some 1
Chondrodysplasia Pathological process Pathological developmental process true Inferred relationship Some 1
Chondrodysplasia Is a Congenital anomaly of skeletal bone true Inferred relationship Some
Chondrodysplasia Associated morphology Congenital dysplasia false Inferred relationship Some 1
Chondrodysplasia Finding site Bone structure false Inferred relationship Some 1
Chondrodysplasia Associated morphology Congenital dysplasia false Inferred relationship Some 1
Chondrodysplasia Is a Congenital skeletal dysplasia true Inferred relationship Some
Chondrodysplasia Occurrence Congenital false Inferred relationship Some 2
Chondrodysplasia Finding site Bone structure false Inferred relationship Some 2
Chondrodysplasia Associated morphology Congenital dysplasia false Inferred relationship Some 2
Chondrodysplasia Occurrence Congenital false Inferred relationship Some
Chondrodysplasia Finding site Skeletal system structure false Inferred relationship Some 1
Chondrodysplasia Associated morphology Dysplasia true Inferred relationship Some 1
Chondrodysplasia Finding site Bone structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Chondrodysplasia with joint dislocations gPAPP type Is a True Chondrodysplasia Inferred relationship Some
Fibrochondrogenesis Is a True Chondrodysplasia Inferred relationship Some
Achondroplasia Is a True Chondrodysplasia Inferred relationship Some
QRICH1-related intellectual disability, chondrodysplasia syndrome Is a True Chondrodysplasia Inferred relationship Some
Lethal chondrodysplasia with fragmented bone Is a True Chondrodysplasia Inferred relationship Some
Lethal retarded ossification syndromes Is a True Chondrodysplasia Inferred relationship Some
Multiple exostosis syndromes Is a False Chondrodysplasia Inferred relationship Some
Chondrodysplasia, unspecified Is a False Chondrodysplasia Inferred relationship Some
Dyschondroplasia NOS Is a False Chondrodysplasia Inferred relationship Some
Brachydactylous dwarfism Mseleni type Is a True Chondrodysplasia Inferred relationship Some
Lethal recessive chondrodysplasia Is a True Chondrodysplasia Inferred relationship Some
X-linked dominant chondrodysplasia Chassaing Lacombe type Is a True Chondrodysplasia Inferred relationship Some
Camptodactyly with fibrous tissue hyperplasia and skeletal dysplasia syndrome Is a True Chondrodysplasia Inferred relationship Some
Chondrodysplasia with disorder of sex development syndrome Is a True Chondrodysplasia Inferred relationship Some
Bone dysplasia lethal Holmgren type Is a True Chondrodysplasia Inferred relationship Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Musculoskeletal finding reference set

Problem/Diagnosis reference set

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