MeSH Browser

MeSH Supplementary: O'Donnell-Luria-Rodan syndrome
Unique ID: C000730747
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C000730747
Entry Term(s): ODLURO syndrome
Heading Mapped to: *Autistic Disorder; *Developmental Disabilities; *Epilepsy; *Facies
Note: Disorder characterized by global developmental delay, autism, epilepsy, hypotonia, and mild facies. It is caused by mutations in the KMT2E gene. OMIM: 618512
Date of Entry: 2024/05/23
Revision Date: 2024/05/23

O'Donnell-Luria-Rodan syndrome MeSH Supplementary Concept Data 2025