Saul-Wilson syndrome

A bone development disease characterized by early developmental delay primarily involving speech, distinct facial features, short stature, brachydactyly, clubfoot deformities, cataracts, and microcephaly that has_material_basis_in heterozygous mutation in the COG4 gene on chromosome 16q22.1.

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.

bile duct mucoepidermoid carcinoma

A mucoepidermoid carcinoma located_in a bile duct.

fungal meningitis

A meningitis that has_material_basis_in a fungal infection.