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1285518004: Wolfram-syndroom type 1 (aandoening)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Jun 2023. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5247892011 Wolfram syndrome type I en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5247893018 Wolfram syndrome type 1 (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
5247894012 Wolfram syndrome type 1 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5247895013 WFS1 - Wolfram syndrome-1 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
14436091000146117 DIDMOAD-syndroom type 1 nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
14436101000146112 syndroom van Wolfram type 1 nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
14436111000146114 Wolfram-syndroom type 1 nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
14436121000146116 Wolfram-syndroom type 1 (aandoening) nl Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
5247902016 A rare genetic endocrine disorder with characteristics of type 1 diabetes mellitus (DM), diabetes insipidus (DI), sensorineural deafness (D), bilateral optical atrophy (OA) and neurological signs. Type 1 has onset in the first decade with diabetes mellitus and optic atrophy manifestations. 50% of patients also develop diabetes insipidus. Additional features may include urinary tract abnormalities, neurological involvement and psychiatric manifestations. Caused by caused by homozygous or compound heterozygous mutation in the gene encoding wolframin (WFS1) on chromosome 4p16. Transmission is autosomal recessive. 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
Wolfram syndrome type 1 (disorder) Is a Wolfram syndrome true Inferred relationship Some
Wolfram syndrome type 1 (disorder) Finding site Structure of auditory system (body structure) true Inferred relationship Some 5
Wolfram syndrome type 1 (disorder) Interprets Hearing true Inferred relationship Some 3
Wolfram syndrome type 1 (disorder) Has interpretation Decreased true Inferred relationship Some 3
Wolfram syndrome type 1 (disorder) Finding site Structure of left optic nerve (body structure) true Inferred relationship Some 1
Wolfram syndrome type 1 (disorder) Associated morphology Atrophy true Inferred relationship Some 1
Wolfram syndrome type 1 (disorder) Finding site Structure of right optic nerve (body structure) true Inferred relationship Some 2
Wolfram syndrome type 1 (disorder) Associated morphology Atrophy true Inferred relationship Some 2
Wolfram syndrome type 1 (disorder) Finding site Structure of endocrine system (body structure) true Inferred relationship Some 4

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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