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Google OMIM PubMed Wikipedia [AI, hypoplastic/hypomaturation, X-linked] [AI, pigmented hypomaturation type] [AI1B] [AI1G] [AIH and openbite malocclusion, autosomal recessive] [AIH1] [AIH2] [Cone-rod dystrophy and AI] Amelogenesis imperfecta [Clinical features: defect of dental enamel formation; yellow, brown or grey teeth] |
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Amelogenesis imperfecta |
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Orphanet Journal of Rare Diseases |