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-optic atrophy syndrome

Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy

This is just here as a test because I lose it

Term information

database cross reference
expertlink
  • https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2836
hasDbXref
  • UMLS:C0796122
  • ICD-10:G31.8
  • OMIM:260565
  • MeSH:C536317
  • UMLS:C1850055
has age of onset
  • http://www.orpha.net/ORDO/Orphanet_409945
  • http://www.orpha.net/ORDO/Orphanet_409944
has inheritance
  • http://www.orpha.net/ORDO/Orphanet_409929
  • http://www.orpha.net/ORDO/Orphanet_409930
has point prevalence range
  • http://www.orpha.net/ORDO/Orphanet_409981
notation
  • ORPHA:2836
part of
  • http://www.orpha.net/ORDO/Orphanet_441434
  • http://www.orpha.net/ORDO/Orphanet_182070
  • http://www.orpha.net/ORDO/Orphanet_568047
  • http://www.orpha.net/ORDO/Orphanet_166463
  • http://www.orpha.net/ORDO/Orphanet_183500
present in
  • http://www.orpha.net/ORDO/Orphanet_409991