ALPHA-METHYLACYL-CoA RACEMASE DEFICIENCY; AMACRD |
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ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY TYPE 1 |
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ALPHA-THALASSEMIA |
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ALPHA-THALASSEMIA MYELODYSPLASIA SYNDROME; ATMDS |
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ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, CHROMOSOME 16-RELATED |
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ALPHA/BETA T-CELL LYMPHOPENIA WITH GAMMA/DELTA T-CELL EXPANSION, SEVERE CYTOMEGALOVIRUS INFECTION, AND AUTOIMMUNITY |
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ALPORT SYNDROME, AUTOSOMAL DOMINANT |
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ALPORT SYNDROME, X-LINKED; ATS |
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ALSTROM SYNDROME; ALMS |
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ALTERNATING HEMIPLEGIA OF CHILDHOOD 1; AHC1 |
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ALTERNATING HEMIPLEGIA OF CHILDHOOD 2; AHC2 |
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ALVEOLAR CAPILLARY DYSPLASIA WITH MISALIGNMENT OF PULMONARY VEINS; ACDMPV |
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ALVEOLAR SOFT PART SARCOMA; ASPS |
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ALZHEIMER DISEASE 2; AD2 |
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ALZHEIMER DISEASE 4 |
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ALZHEIMER DISEASE; AD |
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AMEGAKARYOCYTIC THROMBOCYTOPENIA, CONGENITAL; CAMT |
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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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