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720753002: Cranioosteoarthropathy (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3322004019 Cranioosteoarthropathy (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3322005018 Cranioosteoarthropathy en Synonym Active Entire term case insensitive SNOMED CT core module
3322006017 Cranio-osteoarthropathy en Synonym Active Entire term case insensitive SNOMED CT core module
3322007014 Currarino disease en Synonym Active Entire term case sensitive SNOMED CT core module
3322008016 Currarino idiopathic osteoarthropathy en Synonym Active Entire term case sensitive SNOMED CT core module
3322009012 Reginato Schiapachasse syndrome en Synonym Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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