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| Term | amelogenesis imperfecta type 2A6 | ID (Ontology) | DOID:0080960 (Human Disease) |
| Definition | An amelogenesis imperfecta that is characterized by enamel of normal thickness that is hypomineralized and has a mottled appearance and that has_material_basis_in homozygous mutation in the G protein-coupled receptor-68 (GPR68) on chromosome 14q32. | ||
| Also Known As | "Amelogenesis imperfecta, hypomaturation type, IIA6" | ||
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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autosomal genetic disease |__autosomal recessive disease__ dental enamel hypoplasia | |__amelogenesis imperfecta______| amelogenesis imperfecta type 2A6 |
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| Is a |
autosomal recessive disease amelogenesis imperfecta |
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| MIM:617217 | |||