diabetes mellitus and insipidus with optic atrophy and deafness

Preferred Label : diabetes mellitus and insipidus with optic atrophy and deafness;

Details

Origin ID

DB-61790;

UMLS CUI

C0043207;

Automatic exact mappings (from CISMeF team)
- Wolfram syndrome [ICD-11 More detail]
- Wolfram syndrome [MedDRA Preferred Term]
Currated CISMeF NLP mapping
- Diabetes mellitus AND insipidus with optic atrophy AND deafness (disorder) [SNOMED CT concept]
- Wolfram Syndrome [NCIt concept]
- Wolfram syndrome [PASCAL descriptor]
- Wolfram syndrome [DO Concept]
- Wolfram syndrome [ORDO Disease]
- Wolfram syndrome 1 [DO Concept]
- Wolfram syndrome 1 [OMIM Phenotype]
- wolfram syndrome [MeSH Descriptor]
- wolfram syndrome [MeSH concept]
ICD-10 exact mapping(s)
- Other specified endocrine disorders [ICD-10 Sub-category (who)]
Manual NTBT mappings (CISMeF)
- Autosomal recessive syndromic optic atrophy [ORDO Disease]
- Rare diabetes mellitus type 1 [ORDO Disease]
- Rare genetic diabetes mellitus [ORDO Disease]
Metaterm(s)
- endocrinology [CISMeF Metaterm]
- metabolism [CISMeF Metaterm]
SNOMED CT concept
- Diabetes mellitus AND insipidus with optic atrophy AND deafness (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- DIDMOAD syndrome [MedDRA LLT]
- Diabetes mellitus AND insipidus with optic atrophy AND deafness (disorder) [SNOMED CT concept]
- Wolfram Syndrome [NCIt concept]
- Wolfram syndrome [ORDO Disease]
- Wolfram syndrome [Disease (Nov.)]
- Wolfram syndrome [DO Concept]
- Wolfram syndrome [PASCAL descriptor]
- Wolfram syndrome [MedDRA Preferred Term]
- Wolfram syndrome 1 [OMIM Phenotype]
- Wolfram syndrome 1 [DO Concept]
- wolfram syndrome [MeSH Descriptor]
- wolfram syndrome [MeSH concept]

Keyword's position in hierarchy(ies) :

Main resources

You can consult :

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