ALZHEIMER DISEASE; AD |
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AMEGAKARYOCYTIC THROMBOCYTOPENIA, CONGENITAL; CAMT |
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AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA1; AI2A1 |
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AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA2; AI2A2 |
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AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA5; AI2A5 |
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AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA6; AI2A6 |
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AMELOGENESIS IMPERFECTA, TYPE IA; AI1A |
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AMELOGENESIS IMPERFECTA, TYPE IG; AI1G |
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AMELOGENESIS IMPERFECTA, TYPE IIIA; AI3A |
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AMELOGENESIS IMPERFECTA, TYPE IJ; AI1J |
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AMELOGENESIS IMPERFECTA, TYPE IV; AI4 |
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AMELOGENESIS IMPERFECTA-GINGIVAL HYPERPLASIA SYNDROME |
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AMINOACYLASE 1 DEFICIENCY; ACY1D |
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AMYLOIDOSIS, FINNISH TYPE |
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AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED |
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AMYOTROPHIC LATERAL SCLEROSIS 11; ALS11 |
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AMYOTROPHIC LATERAL SCLEROSIS 12; ALS12 |
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AMYOTROPHIC LATERAL SCLEROSIS 14 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA; ALS14 |
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AMYOTROPHIC LATERAL SCLEROSIS 16, JUVENILE; ALS16 |
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AMYOTROPHIC LATERAL SCLEROSIS 17; ALS17 |
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