MeSH Browser

MeSH Supplementary: PEHO syndrome
Unique ID: C536317
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536317
Entry Term(s): Infantile cerebellooptic atrophy; PEHO-Like Syndrome; Progressive Encephalopathy with edema, Hypsarrhythmia, and Optic atrophy
Heading Mapped to: *Brain Edema; *Optic Atrophy; *Spasms, Infantile; *Neurodegenerative Diseases
Frequency: 16
Date of Entry: 2010/08/25
Revision Date: 2012/11/05

PEHO syndrome MeSH Supplementary Concept Data 2024