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717944002: branchiogene doofheidsyndroom (aandoening)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3324418016 Branchiogenic deafness syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3324419012 Branchiogenic deafness syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3324420018 Megarbane Loiselet syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
6055351000146119 branchiogene doofheidsyndroom nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6055361000146116 syndroom van Mégarbané-Loiselet nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6055371000146110 branchiogene doofheidsyndroom (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
3324421019 A multiple congenital anomalies syndrome, described in one family to date, with characteristics of branchial cysts or fistula, ear malformations, congenital hearing loss (conductive, sensorineural, and mixed), internal auditory canal hypoplasia, strabismus, trismus, abnormal fifth fingers, vitiliginous lesions, short stature and mild learning disability. Renal and urethral abnormalities are absent. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Branchiogenic deafness syndrome (disorder) Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Branchiogenic deafness syndrome (disorder) Is a Multiple system malformation syndrome true Inferred relationship Some
Branchiogenic deafness syndrome (disorder) Is a Congenital anomaly of ear with impairment of hearing true Inferred relationship Some
Branchiogenic deafness syndrome (disorder) Is a Auditory system hereditary disorder true Inferred relationship Some
Branchiogenic deafness syndrome (disorder) Interprets Hearing true Inferred relationship Some 2
Branchiogenic deafness syndrome (disorder) Interprets observatie betreffende functioneren false Inferred relationship Some
Branchiogenic deafness syndrome (disorder) Associated morphology gebrekkige ontwikkeling (afwijkende morfologie) false Inferred relationship Some 3
Branchiogenic deafness syndrome (disorder) Occurrence Congenital false Inferred relationship Some 3
Branchiogenic deafness syndrome (disorder) Finding site Ear structure false Inferred relationship Some 3
Branchiogenic deafness syndrome (disorder) Finding site Ear structure true Inferred relationship Some 1
Branchiogenic deafness syndrome (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 1
Branchiogenic deafness syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Branchiogenic deafness syndrome (disorder) Occurrence Congenital true Inferred relationship Some 1
Branchiogenic deafness syndrome (disorder) Is a Developmental hereditary disorder true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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