Miller-Dieker lissencephaly syndrome

A syndrome characterized by classical lissencephaly and distinct facial features and has_material_basis_in submicroscopic deletions of 17p13.3, including the LIS1 gene.

Miller Fisher syndrome

A Guillain-Barre syndrome that manifests as a descending paralysis. It usually affects the eye muscles first and presents with the triad of ophthalmoplegia, ataxia, and areflexia.

postaxial acrofacial dysostosis

A syndrome characterized by severe micrognathia, cleft lip and/or palate, hypoplasia or aplasia of the postaxial elements of the limbs, coloboma of the eyelids, cup-shaped ears, and supernumerary nipples that has_material_basis_in homozygous or compound heterozygous mutation in DHODH on 16q22.2.

3-M syndrome

A syndrome characterized by dwarfism, facial dysmorphia and skeletal abnormalities.

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.

viral meningitis

A meningitis that has_material_basis_in a viral infection.