FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.8.2  |  FHIR Version n/a  User: [n/a]

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
2709861000005110 Williams' syndrom da Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Danish 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 (disorder) 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 struktur af urinvejene false Inferred relationship Some
Williams syndrome Associated morphology Kongenit malformation false Inferred relationship Some
Williams syndrome Associated morphology kongenit anomali false Inferred relationship Some 1
Williams syndrome Finding site Urinary tract includes entire kidney and the urinary tract proper which relate to the ureter, bladder and urethra. false Inferred relationship Some 3
Williams syndrome Occurrence Congenital true Inferred relationship Some 1
Williams syndrome Associated morphology dysgenese 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 Pathological process (attribute) 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 (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

This concept is not in any reference sets

Back to Start