DISEASES

Disease-gene associations mined from literature

Human genes for lissencephaly 10

Lissencephaly 10 [DOID:0112229]

A lissencephaly characterized by variably delayed development, mildly to moderately impaired intellectual development and language delay, seizures, brain features consistent with neuronal migration defects that has_material_basis_in heterozygous mutation in CEP85L on chromosome 6q22.31.

Synonyms:  lissencephaly 10,  DOID:0112229,  LIS10