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63247009: Williams syndrome (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
105139014 Williams syndrome en Synonym Active Case sensitive SNOMED CT core
1232445010 William syndrome en Synonym Active Case sensitive SNOMED CT core
3791530012 Williams Beuren syndrome en Synonym Active Case sensitive SNOMED CT core
3791531011 Deletion 7q11.23 en Synonym Active Case insensitive SNOMED CT core
3791532016 Monosomy 7q11.23 en Synonym Active Case insensitive SNOMED CT core
802509010 Williams syndrome (disorder) en Fully specified name Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Williams syndrome Pathological process Pathological developmental process true Inferred relationship Some 1
Williams syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Some 5
Williams syndrome Associated morphology Morphologically abnormal structure 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 true Inferred relationship Some 3
Williams syndrome Finding site Long arm of chromosome true Inferred relationship Some 1
Williams syndrome Associated morphology Partial monosomy true Inferred relationship Some 2
Williams syndrome Finding site Connective tissue structure true Inferred relationship Some 3
Williams syndrome Associated morphology Partial monosomy true Inferred relationship Some 1
Williams syndrome Is a Genetic disease true Inferred relationship Some
Williams syndrome Pathological process Pathological developmental process true Inferred relationship Some 4
Williams syndrome Pathological process Pathological developmental process true Inferred relationship Some 5
Williams syndrome Pathological process Pathological developmental process true Inferred relationship Some 2
Williams syndrome Is a 7q partial monosomy true Inferred relationship Some
Williams syndrome Pathological process Pathological developmental process true Inferred relationship Some 3
Williams syndrome Is a Congenital heart disease true Inferred relationship Some
Williams syndrome Finding site Structure of heart 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
Williams syndrome Associated morphology Congenital malformation false Inferred relationship Some
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 Associated morphology Congenital anomaly false Inferred relationship Some 1
Williams syndrome Finding site Urinary system structure false Inferred relationship Some 3
Williams syndrome Occurrence Congenital true Inferred relationship Some 1
Williams syndrome Associated morphology Developmental abnormality false Inferred relationship Some 1
Williams syndrome Occurrence Congenital true Inferred relationship Some 2
Williams syndrome Associated morphology Morphologically abnormal structure 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 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

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Cardiovascular finding reference set

Problem/Diagnosis reference set

Description inactivation indicator reference set

REPLACED BY association reference set

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