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PEHO syndrome

^ http://www.orpha.net/ORDO/Orphanet_2836


PEHO (Progressive encephalopathy with Edema, Hypsarrhythmia and Optic atrophy) syndrome is a rare neurodegenerative disorder belonging to the group of infantile progressive encephalopathies.

Synonyms: Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy, Progressive encephalopathy-optic atrophy syndrome

Term info

database cross reference
  • UMLS:C0796122 (E (exact mapping (the terms and the concepts are equivalent)))
  • UMLS:C1850055 (E (exact mapping (the terms and the concepts are equivalent)))
  • OMIM:260565 (E (exact mapping (the terms and the concepts are equivalent)))
  • MeSH:C536317 (E (exact mapping (the terms and the concepts are equivalent)))
  • ICD-10:G31.8 (NTBT (narrower term maps to a broader term))
  • ICD-10:G31.8 (Attributed)
hasDbXref

UMLS:C1850055, MeSH:C536317, UMLS:C0796122, OMIM:260565, ICD-10:G31.8

notation

ORPHA:2836