MeSH Browser

MeSH Supplementary: Fryns-Aftimos Syndrome
Unique ID: C565258
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C565258
Entry Term(s): Cerebrooculofacial Lymphatic Syndrome; Mental Retardation with Epilepsy and Characteristic Facies; Pachygyria, Mental Retardation, Epilepsy, and Characteristic Facies
Registry Number: 0
Heading Mapped to: *Epilepsy; *Intellectual Disability; *Facies; *Craniofacial Abnormalities; *Lissencephaly
Frequency: 6
Date of Entry: 2012/11/05

Fryns-Aftimos Syndrome MeSH Supplementary Concept Data 2024