FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.10  |  FHIR Version n/a  User: [n/a]

254273005: Autosomal deletion - mosaicism (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
378507017 Autosomal deletion - mosaicism en Synonym Active Case insensitive SNOMED CT core
645143015 Autosomal deletion - mosaicism (disorder) en Fully specified name Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal deletion - mosaicism Associated morphology Mosaicism true Inferred relationship Some 1
Autosomal deletion - mosaicism Associated morphology Congenital anomaly false Inferred relationship Some 1
Autosomal deletion - mosaicism Finding site Chromosome structure false Inferred relationship Some 1
Autosomal deletion - mosaicism Associated morphology Congenital anomaly false Inferred relationship Some
Autosomal deletion - mosaicism Finding site Chromosome structure false Inferred relationship Some 1
Autosomal deletion - mosaicism Is a Monosomy and deletion from autosome true Inferred relationship Some
Autosomal deletion - mosaicism Occurrence Congenital true Inferred relationship Some 1
Autosomal deletion - mosaicism Associated morphology Cellular AND/OR subcellular abnormality false Inferred relationship Some 1
Autosomal deletion - mosaicism Finding site Chromosome true Inferred relationship Some 1
Autosomal deletion - mosaicism Occurrence Congenital false Inferred relationship Some
Autosomal deletion - mosaicism Associated morphology Alteration of chromosome structure false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start