FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.21  |  FHIR Version n/a  User: [n/a]

717157006: Trisomy 10p (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2016. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3308544019 Trisomy 10p (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3308545018 Trisomy 10p en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Trisomy 10p Is a Anomaly of chromosome pair 10 false Inferred relationship Existential restriction modifier
Trisomy 10p Is a Multiple malformation syndrome with facial-limb defects as major feature true Inferred relationship Existential restriction modifier
Trisomy 10p Is a Mental retardation false Inferred relationship Existential restriction modifier
Trisomy 10p Is a Trisomy and partial trisomy of autosome false Inferred relationship Existential restriction modifier
Trisomy 10p Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 3
Trisomy 10p Occurrence Congenital true Inferred relationship Existential restriction modifier 3
Trisomy 10p Finding site Limb structure true Inferred relationship Existential restriction modifier 3
Trisomy 10p Associated morphology Trisomy false Inferred relationship Existential restriction modifier 4
Trisomy 10p Occurrence Congenital false Inferred relationship Existential restriction modifier 4
Trisomy 10p Finding site Chromosome pair 10 false Inferred relationship Existential restriction modifier 4
Trisomy 10p Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 5
Trisomy 10p Occurrence Congenital false Inferred relationship Existential restriction modifier 5
Trisomy 10p Finding site Face structure false Inferred relationship Existential restriction modifier 5
Trisomy 10p Is a Intellectual disability true Inferred relationship Existential restriction modifier
Trisomy 10p Is a Trisomy 10 true Inferred relationship Existential restriction modifier
Trisomy 10p Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Trisomy 10p Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Trisomy 10p Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Trisomy 10p Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 3
Trisomy 10p Finding site Chromosome pair 10 true Inferred relationship Existential restriction modifier 1
Trisomy 10p Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 3
Trisomy 10p Associated morphology Trisomy true Inferred relationship Existential restriction modifier 1
Trisomy 10p Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Trisomy 10p Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 2
Trisomy 10p Finding site Face structure true Inferred relationship Existential restriction modifier 2
Trisomy 10p Interprets Intellectual ability true Inferred relationship Existential restriction modifier 4
Trisomy 10p Has interpretation Impaired true Inferred relationship Existential restriction modifier 4
Trisomy 10p Interprets Adaptation behavior true Inferred relationship Existential restriction modifier 5
Trisomy 10p Has interpretation Impaired true Inferred relationship Existential restriction modifier 5

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start