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21086008: Cockayne syndrome (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
35440018 Cockayne syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
35441019 Cokayne syndrome en Synonym Inactive Only initial character case insensitive SNOMED CT core module
213719011 Dwarfism-retinal atrophy-deafness syndrome en Synonym Inactive Only initial character case insensitive SNOMED CT core module
750341017 Cockayne syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module

4 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Cockayne syndrome Is a Multiple malformation syndrome with senile-like appearance true Inferred relationship Existential restriction modifier
Cockayne syndrome Is a Disorder of the central nervous system false Inferred relationship Existential restriction modifier
Cockayne syndrome Is a Congenital anomaly of nervous system false Inferred relationship Existential restriction modifier
Cockayne syndrome Finding site Structure of central nervous system false Inferred relationship Existential restriction modifier 1
Cockayne syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier
Cockayne syndrome Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier 1
Cockayne syndrome Is a Congenital anomaly of central nervous system true Inferred relationship Existential restriction modifier
Cockayne syndrome Finding site Structure of central nervous system false Inferred relationship Existential restriction modifier 1
Cockayne syndrome Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier 1
Cockayne syndrome Is a Hereditary disorder of nervous system true Inferred relationship Existential restriction modifier
Cockayne syndrome Is a Hereditary cancer-predisposing syndrome true Inferred relationship Existential restriction modifier
Cockayne syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Cockayne syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
Cockayne syndrome Finding site Structure of central nervous system false Inferred relationship Existential restriction modifier 2
Cockayne syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Cockayne syndrome Finding site Structure of central nervous system true Inferred relationship Existential restriction modifier 1
Cockayne syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Cockayne syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Cockayne syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
Xeroderma pigmentosum and Cockayne syndrome complex Is a True Cockayne syndrome Inferred relationship Existential restriction modifier
Cockayne syndrome type 3 Is a True Cockayne syndrome Inferred relationship Existential restriction modifier
Cockayne syndrome type 1 Is a True Cockayne syndrome Inferred relationship Existential restriction modifier
Cockayne syndrome type 2 Is a True Cockayne syndrome Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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