Amelogenesis imperfecta (disorder)
| Code | 78494001 |
|---|---|
| Semantic tag | disorder |
| Module | international |
| Definition | defined |
| Effective time | 20190731 |
422977003Congenital anomaly of tooth
disorder
363070008Developmental hereditary disorder
disorder
46557008Disorder of hard tissues of teeth
disorder
1148766007Hereditary disorder of tooth
disorder
699382004Agenesis of enamel
disorder
109478007Amelocerebrohypohidrotic syndrome
disorder
707607008Amelogenesis imperfecta and gingival hyperplasia syndrome
disorder
707608003Amelogenesis imperfecta co-occurrent with cone rod dystrophy
disorder
109471001Amelogenesis imperfecta, hypocalcification type
disorder
109475005Amelogenesis imperfecta, hypomaturation type
disorder
109476006Amelogenesis imperfecta, hypoplastic type
disorder
1279835008Ectodermal dysplasia, hyperhidrosis, cutaneous syndactyly syndrome
disorder
109477002Enamel-renal syndrome
disorder
773692000Late-onset localised junctional epidermolysis bullosa, intellectual disability syndrome
disorder
726672000Short stature, unique facies, enamel hypoplasia, progressive joint stiffness, high-pitched voice syndrome
disorder
733072002Stimmler syndrome
disorder
719911000Trichodysplasia with amelogenesis imperfecta syndrome
disorder
716195006Verloes Bourguignon syndrome
disorder