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

699306003: Chromosome 1p36 deletion syndrome (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2014. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
2983611014 Distal monosomy 1p36 en Synonym Active Entire term case insensitive SNOMED CT core module
2983665014 Monosomy 1p36 syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
2983669015 Chromosome 1p36 deletion syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
2983672010 Chromosome 1p36 deletion syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
2983739016 1p36 deletion syndrome 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
Chromosome 1p36 deletion syndrome Is a Anomaly of chromosome pair 1 false Inferred relationship Existential restriction modifier
Chromosome 1p36 deletion syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier
Chromosome 1p36 deletion syndrome Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier
Chromosome 1p36 deletion syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Chromosome 1p36 deletion syndrome Finding site Chromosome pair 1 false Inferred relationship Existential restriction modifier 1
Chromosome 1p36 deletion syndrome Is a Deletion of part of autosome false Inferred relationship Existential restriction modifier
Chromosome 1p36 deletion syndrome Associated morphology Partial monosomy true Inferred relationship Existential restriction modifier 1
Chromosome 1p36 deletion syndrome Is a Deletion of part of chromosome 1 false Inferred relationship Existential restriction modifier
Chromosome 1p36 deletion syndrome Is a 1p partial monosomy true Inferred relationship Existential restriction modifier
Chromosome 1p36 deletion syndrome Associated morphology Deletion of short arm false Inferred relationship Existential restriction modifier 2
Chromosome 1p36 deletion syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Chromosome 1p36 deletion syndrome Finding site Chromosome pair 1 true Inferred relationship Existential restriction modifier 2
Chromosome 1p36 deletion syndrome Finding site Short arm of chromosome true Inferred relationship Existential restriction modifier 1
Chromosome 1p36 deletion syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Chromosome 1p36 deletion syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Chromosome 1p36 deletion syndrome Associated morphology Partial monosomy true Inferred relationship Existential restriction modifier 2
Chromosome 1p36 deletion syndrome Is a Congenital malformation true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start