Conditions / Genetic
non-syndromic X-linked intellectual disability 101
info · Genetic
A non-syndromic X-linked intellectual disability characterized by global developmental delay that has_material_basis_in hemizygous mutation in the MID2 gene on chromosome Xq22.3.
Signs and symptoms
- Global developmental delay
- Hyperactivity
- Intellectual disability
- Poor speech
- Strabismus
- Long face
- Seizure
- Macrotia
- Optic atrophy
- Clinodactyly
Also known as: MRX101; X-linked mental retardation 101