Disease-gene associations mined from literature

Human genes for Aicardi syndrome

Aicardi syndrome [DOID:8461]

A syndrome that is characterized by absence or underdeveloped tissue connecting the left and right halves of the brain, infantile spasms and chorioretinal lacunae, which are defects in the light-sensitive tissue at the back of the eye.

Synonyms:  Aicardi syndrome,  Aicardi disease,  Aicardi disorder,  DOID:8461

Linkouts:  OMIM