ACROMESOMELIC DYSPLASIA, HUNTER-THOMPSON TYPE; AMDH |
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ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE; AMDM |
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ACROMICRIC DYSPLASIA; ACMICD |
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ACROOSTEOLYSIS DOMINANT TYPE |
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ACTH DEFICIENCY, ISOLATED; IAD |
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ACTH-INDEPENDENT MACRONODULAR ADRENAL HYPERPLASIA 2; AIMAH2 |
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ACTH-INDEPENDENT MACRONODULAR ADRENAL HYPERPLASIA; AIMAH1 |
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ACUTE PROMYELOCYTIC LEUKEMIA; APL |
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ACYL-CoA DEHYDROGENASE, SHORT-CHAIN, DEFICIENCY OF; ACADSD |
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ACYL-CoA DEHYDROGENASE, VERY LONG-CHAIN, DEFICIENCY OF; ACADVLD |
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ADAMS-OLIVER SYNDROME 1; AOS1 |
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ADAMS-OLIVER SYNDROME 2; AOS2 |
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ADAMS-OLIVER SYNDROME 5; AOS5 |
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ADENINE PHOSPHORIBOSYLTRANSFERASE DEFICIENCY; APRTD |
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ADENYLATE KINASE DEFICIENCY, HEMOLYTIC ANEMIA DUE TO |
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ADENYLOSUCCINASE DEFICIENCY; ADSLD |
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ADERMATOGLYPHIA; ADERM |
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ADIPONECTIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 1; ADIPQTL1 |
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ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 17-ALPHA-HYDROXYLASE DEFICIENCY |
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ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 3-BETA-HYDROXYSTEROID DEHYDROGENASE 2 DEFICIENCY |
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