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111339003: Congenital anomaly of ear with impairment of hearing (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
178572014 Congenital anomaly of ear with impairment of hearing en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
630484011 Congenital anomaly of ear with impairment of hearing (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
178572014 Congenital anomaly of ear with impairment of hearing en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
178572014 Congenital anomaly of ear with impairment of hearing en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
630484011 Congenital anomaly of ear with impairment of hearing (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
630484011 Congenital anomaly of ear with impairment of hearing (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5970701000241115 anomalie congénitale de l'oreille avec déficience auditive fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5970711000241118 anomalie congénitale de l'oreille avec altération de l'audition fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5970701000241115 anomalie congénitale de l'oreille avec déficience auditive fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5970711000241118 anomalie congénitale de l'oreille avec altération de l'audition fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

28 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital anomaly of ear with impairment of hearing Is a Ear, face and neck congenital anomalies (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of ear with impairment of hearing Is a Congenital anomaly of ear false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of ear with impairment of hearing Associated morphology Congenital impairment false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital anomaly of ear with impairment of hearing Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of ear with impairment of hearing Finding site Ear structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital anomaly of ear with impairment of hearing Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital anomaly of ear with impairment of hearing Finding site Ear structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital anomaly of ear with impairment of hearing Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital anomaly of ear with impairment of hearing Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital anomaly of ear with impairment of hearing Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital anomaly of ear with impairment of hearing Finding site Ear structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital anomaly of ear with impairment of hearing Is a Congenital malformation of ear true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of ear with impairment of hearing Is a Congenital hearing disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of ear with impairment of hearing Is a Hearing loss true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of ear with impairment of hearing Interprets Hearing true Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital anomaly of ear with impairment of hearing Interprets entité observable fonctionnelle false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of ear with impairment of hearing Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital anomaly of ear with impairment of hearing Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital anomaly of ear with impairment of hearing Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital absence of auricle with atresia of auditory canal Is a False Congenital anomaly of ear with impairment of hearing Inferred relationship Existential restriction modifier (core metadata concept)
Congenital absence of auricle with stenosis of auditory canal Is a False Congenital anomaly of ear with impairment of hearing Inferred relationship Existential restriction modifier (core metadata concept)
Congenital absence of external ear Is a False Congenital anomaly of ear with impairment of hearing Inferred relationship Existential restriction modifier (core metadata concept)
Ear pit syndrome Is a True Congenital anomaly of ear with impairment of hearing Inferred relationship Existential restriction modifier (core metadata concept)
Jervell and Lange-Nielsen syndrome (disorder) Is a False Congenital anomaly of ear with impairment of hearing Inferred relationship Existential restriction modifier (core metadata concept)
Jervell and Lange-Nielson syndrome Is a False Congenital anomaly of ear with impairment of hearing Inferred relationship Existential restriction modifier (core metadata concept)
Sellars Beighton syndrome Is a True Congenital anomaly of ear with impairment of hearing Inferred relationship Existential restriction modifier (core metadata concept)
Branchiogenic deafness syndrome (disorder) Is a True Congenital anomaly of ear with impairment of hearing Inferred relationship Existential restriction modifier (core metadata concept)
Bilateral microtia with deafness and cleft palate syndrome (disorder) Is a True Congenital anomaly of ear with impairment of hearing Inferred relationship Existential restriction modifier (core metadata concept)
Thickened earlobe with conductive deafness syndrome (disorder) Is a True Congenital anomaly of ear with impairment of hearing Inferred relationship Existential restriction modifier (core metadata concept)
Congenital conductive hearing loss Is a True Congenital anomaly of ear with impairment of hearing Inferred relationship Existential restriction modifier (core metadata concept)
Postlingual non-syndromic genetic deafness Is a False Congenital anomaly of ear with impairment of hearing Inferred relationship Existential restriction modifier (core metadata concept)
Prelingual non-syndromic genetic deafness (disorder) Is a False Congenital anomaly of ear with impairment of hearing Inferred relationship Existential restriction modifier (core metadata concept)
Congenital malformation of left ear with impairment of hearing Is a True Congenital anomaly of ear with impairment of hearing Inferred relationship Existential restriction modifier (core metadata concept)
Impairment of hearing of right ear co-occurrent and due to congenital ear malformation (disorder) Is a True Congenital anomaly of ear with impairment of hearing Inferred relationship Existential restriction modifier (core metadata concept)
Deafness, vitiligo, achalasia syndrome Is a True Congenital anomaly of ear with impairment of hearing Inferred relationship Existential restriction modifier (core metadata concept)
Congenital deafness with labyrinthine aplasia, microtia and microdontia Is a True Congenital anomaly of ear with impairment of hearing Inferred relationship Existential restriction modifier (core metadata concept)
A rare genetic hematologic disorder characterized by bone marrow failure which manifests with aplastic anemia and/or myelodysplasia, associated with hearing/ear abnormalities (such as deafness, labyrinthitis), inherited in an autosomal dominant manner. Caused by heterozygous mutation in the SRP72 gene on chromosome 4q12. Is a True Congenital anomaly of ear with impairment of hearing Inferred relationship Existential restriction modifier (core metadata concept)
Neutropenia, monocytopenia, deafness syndrome (disorder) Is a True Congenital anomaly of ear with impairment of hearing Inferred relationship Existential restriction modifier (core metadata concept)
Sinoatrial node dysfunction and deafness (disorder) Is a True Congenital anomaly of ear with impairment of hearing Inferred relationship Existential restriction modifier (core metadata concept)
Stapes ankylosis with broad thumb and toe syndrome (disorder) Is a True Congenital anomaly of ear with impairment of hearing Inferred relationship Existential restriction modifier (core metadata concept)
Coxoauricular syndrome (disorder) Is a True Congenital anomaly of ear with impairment of hearing Inferred relationship Existential restriction modifier (core metadata concept)
Branchiootic syndrome Is a True Congenital anomaly of ear with impairment of hearing Inferred relationship Existential restriction modifier (core metadata concept)
Pendred's syndrome Is a True Congenital anomaly of ear with impairment of hearing Inferred relationship Existential restriction modifier (core metadata concept)
X-linked external auditory canal atresia, dilated internal auditory canal, facial dysmorphism syndrome Is a True Congenital anomaly of ear with impairment of hearing Inferred relationship Existential restriction modifier (core metadata concept)
Cardiospondylocarpofacial syndrome (disorder) Is a True Congenital anomaly of ear with impairment of hearing Inferred relationship Existential restriction modifier (core metadata concept)
Congenital cochleovestibular malformation (disorder) Is a True Congenital anomaly of ear with impairment of hearing Inferred relationship Existential restriction modifier (core metadata concept)
Mondini defect (disorder) Is a True Congenital anomaly of ear with impairment of hearing Inferred relationship Existential restriction modifier (core metadata concept)
Choanal atresia, athelia, hypothyroidism, delayed puberty, short stature syndrome (disorder) Is a True Congenital anomaly of ear with impairment of hearing Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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