D2I2.
congenital

Sturge–Weber syndrome

Sturge–Weber , sometimes referred to as encephalotrigeminal angiomatosis, is a rare type of phakomatosis, a disorder that affects the central nervous system, skin, and eyes. It is often associated with port-wine stains of the face. manifestations include glaucoma, choroidal , , intellectual disability, and of the blood of the leptomeninges.

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Plain-language summary adapted from Wikipedia. Not medical advice.