Bell's palsy

A facial paralysis resulting from dysfunction in the cranial nerve VII (facial nerve).

fragile X syndrome

A syndrome that is characterized by moderate to severe mental retardation, macroorchidism, and distinct facial features, including long face, large ears, and prominent jaw, and has_material_basis_in X-linked inheritance and a loss of FMR1 function.

fibrochondrogenesis 1

A fibrochondrogenesis that is characterized by a flat midface with a small nose and anteverted nares, significant shortening of all limb segments but relatively normal hands and feet, and a small bell-shaped thorax with a protuberant abdomen and that has_material_basis_in compound heterozygous mutation in the COL11A1 gene on chromosome 1p21.

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.

bacterial meningitis

A meningitis that has_material_basis_in a bacterial infection.