Congenital enamel hypoplasia | Article about Congenital enamel hypoplasia by The Free Dictionary
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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.
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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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