MRT18 is an autosomal recessive disorder characterized by impaired intellectual development with or without epilepsy. Other features may include spasticity, congenital heart disease, brain abnormalities, and atypical electroencephalography (summary by Trehan et al., 2015). [from OMIM]
- MedGen UID:
- 481895
- •Concept ID:
- C3280265
- •
- Mental or Behavioral Dysfunction