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Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction

MedGen UID:
315660
•Concept ID:
C1809475
•
Disease or Syndrome
Synonyms: Hereditary photomyoclonus associated with diabetes mellitus, deafness, nephropathy, and cerebral dysfunction; Herrmann syndrome
SNOMED CT: Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction (237612000); Herrmann syndrome (237612000)
 
Monarch Initiative: MONDO:0008242
OMIM®: 172500

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