herrmann syndrome

Preferred Label : herrmann syndrome;

MeSH note : Hereditary photomyoclonus associated with diabetes mellitus, deafness, nephropathy, and cerebral dysfunction;

MeSH synonym : photomyoclonus, diabetes mellitus, deafness, nephropathy, and cerebral dysfunction;

Détails

Origin ID

C538113;

UMLS CUI

C1809475;

MeSH term(s) associated for indexing
- cerebellar ataxia [MeSH Descriptor]
- deafness [MeSH Descriptor]
- diabetes mellitus [MeSH Descriptor]
- diabetic neuropathies [MeSH Descriptor]
- kidney diseases [MeSH Descriptor]
- myoclonus [MeSH Descriptor]
Record concept(s)
- Herrmann syndrome [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction (disorder) [SNOMED CT concept]
- Photomyoclonus, diabetes mellitus, deafness, nephropathy, and cerebral dysfunction [OMIM Phenotype]

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