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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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