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63247009: Williams syndrome (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
105139014 Williams syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
802509010 Williams syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
1232445010 William syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3791530012 Williams Beuren syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3791531011 Deletion 7q11.23 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3791532016 Monosomy 7q11.23 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
911741000172113 syndrome de Williams fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)
934761000172117 délétion 7q11.23 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
2191481000172112 monosomie 7q11.23 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
2191491000172110 syndrome de Williams-Beuren fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)
949861000172114 syndroom van Williams nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)
954461000172113 Williams-syndroom nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) Belgian module (core metadata concept)
1011941000172117 deletie 7q11.23 nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
2191471000172114 Williams-Beurensyndroom nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) Belgian module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Williams syndrome Is a Familial idiopathic hypercalciuria false Inferred relationship Some
Williams syndrome Is a Anomaly of chromosome pair 7 false Inferred relationship Some
Williams syndrome Is a Multiple malformation syndrome, moderate short stature, facial false Inferred relationship Some
Williams syndrome Finding site Chromosome pair 7 false Inferred relationship Some 1
Williams syndrome Associated morphology Deletion of long arm false Inferred relationship Some 4
Williams syndrome Occurrence Congenital false Inferred relationship Some
Williams syndrome Finding site Sex chromosome false Inferred relationship Some
Williams syndrome Finding site Urinary tract structure false Inferred relationship Some
Williams syndrome Associated morphology Congenital malformation false Inferred relationship Some
Williams syndrome Associated morphology Congenital anomaly false Inferred relationship Some 1
Williams syndrome Finding site Urinary system structure (body structure) false Inferred relationship Some 3
Williams syndrome Occurrence Congenital true Inferred relationship Some 1
Williams syndrome Associated morphology Developmental anomaly false Inferred relationship Some 1
Williams syndrome Occurrence Congenital true Inferred relationship Some 2
Williams syndrome Associated morphology Morphologically abnormal structure (morphologic abnormality) false Inferred relationship Some 1
Williams syndrome Associated morphology Cellular AND/OR subcellular abnormality false Inferred relationship Some 2
Williams syndrome Finding site Chromosome pair 7 true Inferred relationship Some 2
Williams syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Williams syndrome Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 5
Williams syndrome Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 4
Williams syndrome Finding site Face structure true Inferred relationship Some 5
Williams syndrome Is a Congenital connective tissue disorder true Inferred relationship Some
Williams syndrome Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 3
Williams syndrome Finding site Long arm of chromosome true Inferred relationship Some 1
Williams syndrome Associated morphology Partial monosomy (morphologic abnormality) true Inferred relationship Some 2
Williams syndrome Finding site Connective tissue structure true Inferred relationship Some 3
Williams syndrome Associated morphology Partial monosomy (morphologic abnormality) true Inferred relationship Some 1
Williams syndrome Is a Genetic disease true Inferred relationship Some
Williams syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 4
Williams syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 5
Williams syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Williams syndrome Is a 7q partial monosomy true Inferred relationship Some
Williams syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 3
Williams syndrome Is a Congenital heart disease true Inferred relationship Some
Williams syndrome Finding site Heart structure true Inferred relationship Some 4
Williams syndrome Occurrence Congenital true Inferred relationship Some 3
Williams syndrome Occurrence Congenital true Inferred relationship Some 4
Williams syndrome Occurrence Congenital true Inferred relationship Some 5
Williams syndrome Is a Multiple malformation syndrome with facial defects as major feature true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Belgian subset for medical problems in patient health records

Description inactivation indicator reference set

GB English

US English

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