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51626007: Werner syndrome (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
1231007018 Pangeria en Synonym Active Case insensitive SNOMED CT core
1231008011 Adult progeria en Synonym Active Case insensitive SNOMED CT core
1783826013 Adult premature ageing syndrome en Synonym Active Case insensitive SNOMED CT core
1784214017 Adult premature aging syndrome en Synonym Active Case insensitive SNOMED CT core
789546011 Werner syndrome (disorder) en Fully specified name Active Case sensitive SNOMED CT core
85980017 Werner syndrome en Synonym Active Case sensitive SNOMED CT core
85981018 Progeria of the adult en Synonym Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Werner syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Some 1
Werner syndrome Pathological process Pathological developmental process true Inferred relationship Some 1
Werner syndrome Finding site Skin structure true Inferred relationship Some 1
Werner syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Werner syndrome Is a Developmental hereditary disorder true Inferred relationship Some
Werner syndrome Interprets Height / growth measure true Inferred relationship Some 2
Werner syndrome Is a Congenital anomaly of skin true Inferred relationship Some
Werner syndrome Is a Premature ageing syndrome true Inferred relationship Some
Werner syndrome Associated morphology Congenital malformation false Inferred relationship Some
Werner syndrome Is a Progeria syndrome false Inferred relationship Some
Werner syndrome Is a Multiple malformation syndrome with senile-like appearance true Inferred relationship Some
Werner syndrome Is a Disorder of stature true Inferred relationship Some
Werner syndrome Is a Hereditary neoplastic syndrome true Inferred relationship Some
Werner syndrome Occurrence Congenital true Inferred relationship Some 1
Werner syndrome Associated morphology Developmental abnormality false Inferred relationship Some 1
Werner syndrome Finding site Skin structure false Inferred relationship Some 2
Werner syndrome Occurrence Congenital false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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