DISEASES

Disease-gene associations mined from literature

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Human genes for X-linked lissencephaly 1

X-linked lissencephaly 1 [DOID:0112239]

A lissencephaly characterized by classic lissencephaly and intellectual disability in males that has_material_basis_in mutation in DCX on chromosome Xq23.

Synonyms:  X-linked lissencephaly 1,  DOID:0112239,  Xlinked lissencephaly 1,  lissencephaly type 1 due to doublecortin gene mutation,  XLIS1

The disease-gene associations are derived from automatic text mining of the biomedical literature, manually curated database annotations, cancer mutation data, and genome-wide association studies. The confidence of each association is signified by stars, where ★★★★★ is the highest confidence and ★☆☆☆☆ is the lowest.

Developed by Sune Frankild, Alexander Junge, Albert Pallejà, Dhouha Grissa, Kalliopi Tsafou, and Lars Juhl Jensen from the Novo Nordisk Foundation Center for Protein Research.