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720753002: Cranioosteoarthropathy (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3322004019 Cranioosteoarthropathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3322005018 Cranioosteoarthropathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3322006017 Cranio-osteoarthropathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3322007014 Currarino disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3322008016 Currarino idiopathic osteoarthropathy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3322009012 Reginato Schiapachasse syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3322010019 A form of primary hypertrophic osteoarthropathy with characteristics of delayed closure of the cranial sutures and fontanelles, digital clubbing, arthropathy, and periostosis. To date, about 30 cases have been reported. May also be associated with congenital heart disease. It is caused by mutations in the HPGD gene (4q33-q34) and is inherited as an autosomal recessive trait. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
905941000172111 cranio-ostéo-arthropathie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
911991000172117 maladie de Currarino fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)
970181000172117 cranio-osteoartropathie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
984341000172112 currarino idiopathische osteoartropathie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Cranioosteoarthropathy (disorder) Is a Congenital anomaly of skull true Inferred relationship Some
Cranioosteoarthropathy (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Cranioosteoarthropathy (disorder) Is a Dysplasia with increased bone density (disorder) true Inferred relationship Some
Cranioosteoarthropathy (disorder) Is a Connective tissue hereditary disorder (disorder) false Inferred relationship Some
Cranioosteoarthropathy (disorder) Is a Hereditary disorder of musculoskeletal system true Inferred relationship Some
Cranioosteoarthropathy (disorder) Associated morphology Congenital dysplasia false Inferred relationship Some 2
Cranioosteoarthropathy (disorder) Occurrence Congenital false Inferred relationship Some 2
Cranioosteoarthropathy (disorder) Finding site Bone structure of cranium false Inferred relationship Some 2
Cranioosteoarthropathy (disorder) Occurrence Congenital true Inferred relationship Some 1
Cranioosteoarthropathy (disorder) Associated morphology Congenital dysplasia false Inferred relationship Some 1
Cranioosteoarthropathy (disorder) Finding site Bone structure of cranium true Inferred relationship Some 1
Cranioosteoarthropathy (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Cranioosteoarthropathy (disorder) Associated morphology Dysplasia true Inferred relationship Some 1
Cranioosteoarthropathy (disorder) Interprets Bone density scan true Inferred relationship Some 2
Cranioosteoarthropathy (disorder) Has interpretation Above reference range true Inferred relationship Some 2
Cranioosteoarthropathy (disorder) Is a Developmental hereditary disorder true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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