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278715001: Chondrodysplasia punctata (stippled epiphyses) group (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
415720018 Chondrodysplasia punctata en Synonym Active Case insensitive SNOMED CT core
415721019 Chondrodysplasia punctata (stippled epiphyses) group en Synonym Active Case insensitive SNOMED CT core
671906017 Chondrodysplasia punctata (stippled epiphyses) group (disorder) en Fully specified name Active Case insensitive SNOMED CT core


14 descendants. Search Descendants:

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group
Chondrodysplasia punctata congenita Is a True Chondrodysplasia punctata Inferred relationship Some
Brachytelephalangic chondrodysplasia punctata Is a True Chondrodysplasia punctata Inferred relationship Some
Chondrodysplasia punctata due to maternal autoimmune disease Is a True Chondrodysplasia punctata Inferred relationship Some
Chondrodysplasia punctata, Conradi-Hünermann type Is a False Chondrodysplasia punctata Inferred relationship Some
Lymphopenic agammaglobulinaemia - short-limbed dwarfism syndrome Is a False Chondrodysplasia punctata Inferred relationship Some
Chondrodysplasia punctata, Conradi-Hünermann type Is a True Chondrodysplasia punctata Inferred relationship Some
Chondrodysplasia punctata, X-linked dominant type Is a True Chondrodysplasia punctata Inferred relationship Some
X-linked dominant chondrodysplasia punctata of Happle Is a False Chondrodysplasia punctata Inferred relationship Some
Rhizomelic chondrodysplasia punctata syndrome Is a True Chondrodysplasia punctata Inferred relationship Some
Hyperphosphatasia-osteoectasia syndrome Is a True Chondrodysplasia punctata Inferred relationship Some
Chondrodysplasia punctata Is a False Chondrodysplasia punctata Inferred relationship Some
Chondrodysplasia punctata Toriello type Is a True Chondrodysplasia punctata Inferred relationship Some
Lissencephaly type 3 metacarpal bone dysplasia syndrome Is a True Chondrodysplasia punctata Inferred relationship Some
Chondrodysplasia punctata, X-linked recessive type Is a True Chondrodysplasia punctata Inferred relationship Some
Chondrodysplasia punctata, MT type Is a True Chondrodysplasia punctata 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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