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95828007: Congenital deafness (disorder)

Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
158711011 Congenital deafness en Synonym Active Entire term case insensitive SNOMED CT core module
512317011 Congenital sensorineural deafness en Synonym Inactive Entire term case insensitive SNOMED CT core module
840063013 Congenital deafness (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

6 descendants. Search Descendants:

Expanded Value Set

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

This concept is not in any reference sets

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