LHX5

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Description

The LHX5 (LIM homeobox 5) is a protein-coding gene located on chromosome 12.

LHX5 is also known as -.

Associated Diseases

• type 2 diabetes mellitus
• Chudley-McCullough syndrome
• subcortical band heterotopia
• amelogenesis imperfecta
• lissencephaly due to TUBA1A mutation
• idiopathic hypereosinophilic syndrome
• microcephaly-polymicrogyria-corpus callosum agenesis syndrome
• lissencephaly type 1 due to doublecortin gene mutation
• sub-cortical nodular heterotopia
• polymicrogyria with optic nerve hypoplasia