FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 4.0.3  |  FHIR Version n/a  User: [n/a]

1367900004: 3q26q28 deletion syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Jul 2025. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5465595014 Monosomy 3q26q28 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5465596010 Del(3)(q26q28) en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5465597018 3q26q28 deletion syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5465598011 3q26q28 deletion syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
3q26q28 deletion syndrome (disorder) Is a Autosomal dominant hereditary disorder true Inferred relationship Some
3q26q28 deletion syndrome (disorder) Is a Developmental hereditary disorder true Inferred relationship Some
3q26q28 deletion syndrome (disorder) Is a Deletion of part of long arm of chromosome 3 (disorder) true Inferred relationship Some
3q26q28 deletion syndrome (disorder) Is a Multiple system malformation syndrome true Inferred relationship Some
3q26q28 deletion syndrome (disorder) Occurrence Congenital true Inferred relationship Some 1
3q26q28 deletion syndrome (disorder) Finding site Chromosome pair 3 true Inferred relationship Some 1
3q26q28 deletion syndrome (disorder) Associated morphology Partial monosomy (morphologic abnormality) true Inferred relationship Some 1
3q26q28 deletion syndrome (disorder) Occurrence Congenital true Inferred relationship Some 2
3q26q28 deletion syndrome (disorder) Finding site Long arm of chromosome true Inferred relationship Some 2
3q26q28 deletion syndrome (disorder) Associated morphology Partial monosomy (morphologic abnormality) true Inferred relationship Some 2
3q26q28 deletion syndrome (disorder) Occurrence Congenital true Inferred relationship Some 3
3q26q28 deletion syndrome (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 3
3q26q28 deletion syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start