alstrom syndrome

Preferred Label : alstrom syndrome;

Details

Origin ID

D6-96300;

UMLS CUI

C0268425;

Currated CISMeF NLP mapping
- Alstroem syndrome [MedDRA Preferred Term]
- Alstrom Syndrome [NCIt concept]
- Alstrom syndrome [DO Concept]
- Alstrom syndrome [Disease (Nov.)]
- Alstrom syndrome [OMIM Phenotype]
- Alstrom syndrome [MedDRA LLT]
- Alstrom syndrome (disorder) [SNOMED CT concept]
- Alström syndrome [ICD-11 More detail]
- Alström syndrome [ORDO Disease]
- alstrom syndrome [MeSH Descriptor]
- alstrom syndrome [MeSH concept]
ICD-10 exact mapping(s)
- Other specified congenital malformation syndromes, not elsewhere classified [ICD-10 Sub-category (who)]
Manual NTBT mappings (CISMeF)
- Genetic obesity [ORDO Disease]
- Rare diabetes mellitus type 2 [ORDO Disease]
- Rare genetic diabetes mellitus [ORDO Disease]
- Renal ciliopathy [ORDO Disease]
- Retinal ciliopathy [ORDO Disease]
- Syndrome associated with dilated cardiomyopathy [ORDO Disease]
- Syndromic genetic deafness [ORDO Disease]
- Syndromic rod-cone dystrophy [ORDO Disease]
Metaterm(s)
- metabolism [CISMeF Metaterm]
SNOMED CT concept
- Alstrom syndrome (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Alstroem syndrome [MedDRA Preferred Term]
- Alstrom Syndrome [NCIt concept]
- Alstrom syndrome [MedDRA LLT]
- Alstrom syndrome [OMIM Phenotype]
- Alstrom syndrome [Disease (Nov.)]
- Alstrom syndrome [DO Concept]
- Alstrom syndrome (disorder) [SNOMED CT concept]
- Alström syndrome [ORDO Disease]
- Alström syndrome [ICD-11 More detail]
- alstrom syndrome [MeSH concept]
- alstrom syndrome [MeSH Descriptor]

Keyword's position in hierarchy(ies) :

Main resources

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