amelogenesis imperfecta
(redirected from Congenital enamel hypoplasia)Also found in: Medical.
amelogenesis imperfecta
[‚am·ə·lō‚jen·ə·səs ‚im·pər′fek·tə] (medicine)
An inherited dental disorder that causes defective formation of tooth enamel.
Also found in: Medical.
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- congenital disorder
- congenital disorder
- congenital disorder
- congenital disorder
- Congenital disorder of glycosylation
- Congenital Disorder of Glycosylation Syndrome
- congenital disorder of glycosylation type 1Q
- Congenital Disorder of Glycosylation Type Ia
- Congenital Disorders of the Peripheral Visual System
- Congenital Dyserythropoietic Anaemia Type I
- congenital dyserythropoietic anemia
- Congenital Dyserythropoietic Anemia, type I
- Congenital Dyserythropoietic Anemia, Type II
- Congenital Dyserythropoietic Anemia, Type III
- Congenital Dyserythropoietic Anemias
- congenital dysphagocytosis
- congenital dysphagocytosis
- Congenital Dysplasia of the Hip
- congenital dysplastic angiectasia
- congenital dysplastic angiomatosis
- congenital ectodermal defect
- congenital ectodermal defect
- congenital ectodermal defect
- congenital ectodermal defect
- congenital ectodermal defect
- congenital ectodermal dysplasia
- congenital ectropion
- congenital ectropion
- congenital elephantiasis
- Congenital Elevation of the Fifth Toe
- Congenital enamel hypoplasia
- Congenital Encephalo-Ophthalmic Dysplasia
- Congenital End-Plate Acetylcholinesterase Deficiency
- congenital enzyme deficiency
- congenital enzyme deficiency
- congenital enzyme deficiency
- Congenital epulis
- congenital epulis of newborn
- Congenital erythropoetic porphyria
- Congenital erythropoetic porphyria
- Congenital erythropoetic porphyria
- congenital erythropoietic porphyria
- congenital erythropoietic porphyria
- congenital erythropoietic porphyria
- congenital erythropoietic porphyria
- congenital erythropoietic porphyria
- congenital euryblepharon
- congenital exophthalmos
- congenital exophthalmos
- congenital exophthalmos
- Congenital facial diplegia
- Congenital Factor Transport Deficiency
- congenital familial cholaemia
- Congenital Familial Long QT Syndrome
- Congenital Fiber-Type Disproportion
- Congenital Fiber-Type Disproportion Myopathy
- Congenital Fibrosis of Extraocular Muscles
- congenital fibrosis of extraocular muscles type 3A
- congenital fibrosis of the extraocular muscles
- congenital generalised lipodystrophy
- congenital generalised lipodystrophy of Berardinelli-Seip
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