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| Term | amelogenesis imperfecta | ID (Ontology) | DOID:2187 (Human Disease) |
| Definition | A dental enamel hypoplasia characterized by abnormal enamel formation. | ||
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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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teeth hard tissue disease |__dental enamel hypoplasia |__amelogenesis imperfecta 20 rec. |__amelogenesis imperfecta hypomaturation type 2A2 1 rec. |__amelogenesis imperfecta hypomaturation type 2A3 1 rec. |__amelogenesis imperfecta hypomaturation type 2A4 |__amelogenesis imperfecta hypomaturation type 2A5 3 rec. |__amelogenesis imperfecta type 1A 1 rec. |__amelogenesis imperfecta type 1B |__amelogenesis imperfecta type 1C |__amelogenesis imperfecta type 1E |__amelogenesis imperfecta type 1F |__amelogenesis imperfecta type 1G 1 rec. |__amelogenesis imperfecta type 1H 2 rec. |__amelogenesis imperfecta type 1J 3 rec. |__amelogenesis imperfecta type 1K 2 rec. |__amelogenesis imperfecta type 2A1 5 rec. |__amelogenesis imperfecta type 2A6 |__amelogenesis imperfecta type 3 | |__amelogenesis imperfecta type 3A | |__amelogenesis imperfecta type 3B | |__amelogenesis imperfecta type 3C |__amelogenesis imperfecta type 4 1 rec. |__X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2 |
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| Is a | dental enamel hypoplasia | ||
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External Crossreferences & Linkouts
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GARD:5791 ICD10CM:K00.5 MESH:D000567 MIM:PS104500 ORDO:88661 SNOMEDCT_US_2023_03_01:78494001 UMLS_CUI:C0002452 |
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