FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  FHIR Version n/a  User: [n/a]

43353004: Congenital anomaly of inner ear (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3006548010 Congenital malformation of inner ear en Synonym Active Case insensitive SNOMED CT core
3787195019 Congenital abnormality of inner ear en Synonym Active Case insensitive SNOMED CT core
72332012 Congenital anomaly of inner ear en Synonym Active Case insensitive SNOMED CT core
780355017 Congenital anomaly of inner ear (disorder) en Fully specified name Active Case insensitive SNOMED CT core


25 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital anomaly of inner ear Associated morphology Morphologically abnormal structure true Inferred relationship Some 1
Congenital anomaly of inner ear Pathological process Pathological developmental process true Inferred relationship Some 1
Congenital anomaly of inner ear Is a Congenital anomaly of ear false Inferred relationship Some
Congenital anomaly of inner ear Is a Disorder of inner ear true Inferred relationship Some
Congenital anomaly of inner ear Associated morphology Congenital anomaly false Inferred relationship Some 1
Congenital anomaly of inner ear Finding site Inner ear structure false Inferred relationship Some 1
Congenital anomaly of inner ear Associated morphology Congenital anomaly false Inferred relationship Some 1
Congenital anomaly of inner ear Occurrence Congenital false Inferred relationship Some 2
Congenital anomaly of inner ear Associated morphology Developmental abnormality false Inferred relationship Some 2
Congenital anomaly of inner ear Finding site Inner ear structure false Inferred relationship Some 2
Congenital anomaly of inner ear Is a Congenital anomaly of ear true Inferred relationship Some
Congenital anomaly of inner ear Occurrence Congenital true Inferred relationship Some 1
Congenital anomaly of inner ear Finding site Inner ear structure true Inferred relationship Some 1
Congenital anomaly of inner ear Occurrence Congenital false Inferred relationship Some
Congenital anomaly of inner ear Finding site Inner ear structure false Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Deafness, vitiligo, achalasia syndrome Is a True Congenital anomaly of inner ear Inferred relationship Some
Congenital deafness with labyrinthine aplasia, microtia and microdontia Is a True Congenital anomaly of inner ear Inferred relationship Some
Autosomal dominant aplasia and myelodysplasia Is a True Congenital anomaly of inner ear Inferred relationship Some
Neutropenia, monocytopenia, deafness syndrome Is a True Congenital anomaly of inner ear Inferred relationship Some
Sinoatrial node dysfunction and deafness Is a True Congenital anomaly of inner ear Inferred relationship Some
Congenital cochleovestibular malformation Is a True Congenital anomaly of inner ear Inferred relationship Some
Hutchinson's triad Is a False Congenital anomaly of inner ear Inferred relationship Some
Structural anomaly of the cochlea and vestibular labyrinth Is a True Congenital anomaly of inner ear Inferred relationship Some
Vascular malformation of inner ear Is a True Congenital anomaly of inner ear Inferred relationship Some
Congenital anomaly of membranous labyrinth Is a False Congenital anomaly of inner ear Inferred relationship Some
Inner ear anomalies NOS Is a False Congenital anomaly of inner ear Inferred relationship Some
Congenital aplasia of inner ear Is a True Congenital anomaly of inner ear Inferred relationship Some
Neurofibromatosis type 2 Is a False Congenital anomaly of inner ear Inferred relationship Some
Congenital abnormal shape of inner ear Is a True Congenital anomaly of inner ear Inferred relationship Some
Congenital deafness Is a False Congenital anomaly of inner ear Inferred relationship Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start