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

699254009: Microdeletion of chromosome 15q13.3 (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
2983307014 15q13.3 deletion syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
2983429014 15q13.3 microdeletion en Synonym Active Entire term case insensitive SNOMED CT core module
2983673017 Microdeletion of chromosome 15q13.3 (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3015079019 Microdeletion of chromosome 15q13.3 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
Microdeletion of chromosome 15q13.3 Is a Anomaly of chromosome pair 15 false Inferred relationship Existential restriction modifier
Microdeletion of chromosome 15q13.3 Occurrence Congenital false Inferred relationship Existential restriction modifier
Microdeletion of chromosome 15q13.3 Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier
Microdeletion of chromosome 15q13.3 Associated morphology Deletion of long arm false Inferred relationship Existential restriction modifier 2
Microdeletion of chromosome 15q13.3 Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Microdeletion of chromosome 15q13.3 Finding site Chromosome pair 15 false Inferred relationship Existential restriction modifier 1
Microdeletion of chromosome 15q13.3 Associated morphology Cellular AND/OR subcellular abnormality false Inferred relationship Existential restriction modifier 1
Microdeletion of chromosome 15q13.3 Is a Partial deletion of long arm of chromosome 15 true Inferred relationship Existential restriction modifier
Microdeletion of chromosome 15q13.3 Is a Congenital malformation true Inferred relationship Existential restriction modifier
Microdeletion of chromosome 15q13.3 Finding site Long arm of chromosome true Inferred relationship Existential restriction modifier 1
Microdeletion of chromosome 15q13.3 Associated morphology Partial monosomy true Inferred relationship Existential restriction modifier 1
Microdeletion of chromosome 15q13.3 Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Microdeletion of chromosome 15q13.3 Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Microdeletion of chromosome 15q13.3 Finding site Chromosome pair 15 true Inferred relationship Existential restriction modifier 2
Microdeletion of chromosome 15q13.3 Associated morphology Partial monosomy true Inferred relationship Existential restriction modifier 2
Microdeletion of chromosome 15q13.3 Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start