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1285519007: Wolfram syndrome type 2 (disorder)


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
5247896014 Wolfram syndrome type 2 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5247897017 Wolfram syndrome type II en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5247898010 Wolfram syndrome type 2 (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
5247899019 WFS2 - Wolfram syndrome-2 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5247903014 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 2 patients present early with optic atrophy, diabetes mellitus, deafness and decreased lifespan but without diabetes insipidus. Caused by homozygous mutation in the CISD2 gene on chromosome 4q24. Transmission is autosomal recessive. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5247896014 Wolfram syndrome type 2 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5247897017 Wolfram syndrome type II en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5247898010 Wolfram syndrome type 2 (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
5247899019 WFS2 - Wolfram syndrome-2 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5247903014 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 2 patients present early with optic atrophy, diabetes mellitus, deafness and decreased lifespan but without diabetes insipidus. Caused by homozygous mutation in the CISD2 gene on chromosome 4q24. Transmission is autosomal recessive. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
595461000274119 WFS2 - Wolfram-Syndrom Typ 2 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
595471000274110 Wolfram-Syndrom Typ 2 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
595461000274119 WFS2 - Wolfram-Syndrom Typ 2 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
595471000274110 Wolfram-Syndrom Typ 2 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Wolfram syndrome type 2 Is a Wolfram syndrome (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Wolfram syndrome type 2 Finding site Structure of auditory system (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 5
Wolfram syndrome type 2 Interprets Hearing true Inferred relationship Existential restriction modifier (core metadata concept) 3
Wolfram syndrome type 2 Has interpretation Decreased true Inferred relationship Existential restriction modifier (core metadata concept) 3
Wolfram syndrome type 2 Finding site Structure of left optic nerve (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Wolfram syndrome type 2 Associated morphology Atrophy true Inferred relationship Existential restriction modifier (core metadata concept) 1
Wolfram syndrome type 2 Finding site Structure of right optic nerve (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Wolfram syndrome type 2 Associated morphology Atrophy true Inferred relationship Existential restriction modifier (core metadata concept) 2
Wolfram syndrome type 2 Finding site Structure of endocrine system (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 4

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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