MeSH Browser

MeSH Supplementary: Wittwer syndrome
Unique ID: C536737
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536737
Registry Numbers: 0
Heading Mapped to: *Epilepsy; *Growth Disorders; *X-Linked Intellectual Disability; *Deaf-Blind Disorders
Frequency: 1
Note: Prenatal and postnatal growth retardation, blindness, hearing loss, dysmorphic features, epilepsy, mental retardation and absence of speech
Date of Entry: 2010/08/25
Revision Date: 2012/11/05

Wittwer syndrome MeSH Supplementary Concept Data 2025