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95828007: Congenital deafness (disorder)

Status: current, Defined. Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
158711011 Congenital deafness en Synonym Active Case insensitive SNOMED CT core
840063013 Congenital deafness (disorder) en Fully specified name Active Case insensitive SNOMED CT core

6 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital deafness Associated morphology Morphologically abnormal structure false Inferred relationship Some 1
Congenital deafness Pathological process Pathological developmental process false Inferred relationship Some 1
Congenital deafness Finding site Structure of auditory system true Inferred relationship Some 1
Congenital deafness Is a Complete deafness true Inferred relationship Some
Congenital deafness Interprets Hearing true Inferred relationship Some 2
Congenital deafness Associated morphology Congenital anomaly false Inferred relationship Some 1
Congenital deafness Is a Congenital anomaly of inner ear false Inferred relationship Some
Congenital deafness Is a Congenital hearing disorder true Inferred relationship Some
Congenital deafness Associated morphology Congenital anomaly false Inferred relationship Some 1
Congenital deafness Finding site Inner ear structure false Inferred relationship Some 1
Congenital deafness Interprets Hearing false Inferred relationship Some
Congenital deafness Occurrence Congenital false Inferred relationship Some 2
Congenital deafness Associated morphology Developmental abnormality false Inferred relationship Some 2
Congenital deafness Finding site Inner ear structure false Inferred relationship Some 2
Congenital deafness Occurrence Congenital true Inferred relationship Some 1
Congenital deafness Occurrence Congenital false Inferred relationship Some
Congenital deafness Finding site Inner ear structure false Inferred relationship Some 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Autosomal dominant aplasia and myelodysplasia Is a True Congenital deafness Inferred relationship Some
Congenital prelingual deafness Is a True Congenital deafness Inferred relationship Some
Neutropenia, monocytopenia, deafness syndrome Is a True Congenital deafness Inferred relationship Some
Deafness, vitiligo, achalasia syndrome Is a True Congenital deafness Inferred relationship Some
Congenital deafness with labyrinthine aplasia, microtia and microdontia Is a True Congenital deafness Inferred relationship Some
Sinoatrial node dysfunction and deafness Is a True Congenital deafness Inferred relationship Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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