Amelogenesis imperfecta

Orpha code: 88661OMIM code: 617217

Definicja

A rare genetic odontal or periodontal disorder that represents a group of developmental conditions affecting the structure and clinical appearance of the enamel of all or nearly all the teeth in a more or less equal manner, and which may be associated with morphologic or biochemical changes elsewhere in the body.

Disease data
Klasyfikacja

Disease

Kod ORPHA
88661
Kod OMIM
617217
Kod ICD10
K00.5
Kod ICD11
LA30.6

No additional description.

Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl