Achalasia-addisonianism-alacrimia syndromeAchromatopsia-4Acrodermatitis enteropathicaAdenomas, multiple colorectalAdrenal hyperplasia, congenital, due to 21-hydroxylase deficiencyAdrenoleukodystrophy Afibrinogenemia, congenitalAlkaptonuriaAlport syndrome, autosomal recessiveAlzheimer disease 1, familialAlzheimer disease, type 3Amyloidosis, hereditary, transthyretin-relatedAmyotrophic lateral sclerosis 1Amyotrophic lateral sclerosis and/or frontotemporal dementia Angioedema, hereditary, type IIIArthropathy, progressive pseudorheumatoid, of childhood Ataxia with isolated vitamin E deficiencyAtaxia-telangiectasiaAutoimmune polyendocrinopathy syndrome , type I