Sturge-Weber syndrome

A vascular disease characterized by intracranial vascular anomaly, leptomeningeal angiomatosis, facial cutaneous vascular malformations, and glaucoma that has_material_basis_in somatic mutation in the GNAQ gene on chromosome 9q21.2.

hereditary hemorrhagic telangiectasia

A vascular disease characterized by the presence of multiple arteriovenous malformations that lack intervening capillaries and result in direct connections between arteries and veins.

nodular nonsuppurative panniculitis

Klippel-Trenaunay syndrome

A syndrome that is characterized by large cutaneous hemangiomata with hypertrophy of the related bones and soft tissues.

epidermolysis bullosa simplex localized type

An epidermolysis bullosa simplex that is characterized by skin blistering that begins anytime between childhood and adulthood and is usually limited to the hands and feet.

acute eustachian salpingitis

A otosalpingitis with a sudden onset and a short course.

acute perichondritis of pinna

A perichondritis of auricle with a sudden onset and a short course.

frontonasal dysplasia

A syndrome that is a cleft in thes nose, a broad nose, wide spaced eyes and a widow's peak.

cartilage cancer

A connective tissue tumor that can be a benign chondroma or a maligannt chondrosarcoma.

dental abscess

A tooth disease characterized by a localized collection of pus associated with a tooth.