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, Aicardi syndromes, DOID:8461
Linkouts: OMIM