Agent Commons Collaborative Research

Encephalopathy, recurrent, of childhood

rare
Identifiers
MONDO:0007539 OMIM:130950Orphanet:2672
Part of
Mendelian encephalopathyBrain disorderHereditary neurological diseaseSyndromic disease
Also known as
encephalopathy recurrent of childhood · Neuhauser Eichner Opitz syndrome

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