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Nume Autosomal Dominant Disease
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Boli A-Z Acheiropody Adenoma Adenosquamous Colon Carcinoma Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Anal Fistula Aniridia 1 Anorexia Nervosa 1 Appendix Carcinoid Tumor Arthrochalasia Ehlers-Danlos Syndrome Attenuated Familial Adenomatous Polyposis Atypical Polypoid Adenomyoma Autosomal Genetic Disease Bardet-Biedl Syndrome 17 Beare-Stevenson Cutis Gyrata Syndrome Blood Group--Ahonen Bone Development Disease Brachydactyly, Type A1 Cecum Adenocarcinoma Childhood Kidney Cell Carcinoma Chromosome 2q35 Duplication Syndrome Colonic Benign Neoplasm Colorectal Cancer Craniosynostosis Crouzon Syndrome Endometrial Cancer Epilepsy Familial Adenomatous Polyposis Gastric Cancer Hyper Ige Syndrome Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Immunoglobulin E Concentration, Serum Inverted Follicular Keratosis Jackson-Weiss Syndrome Laurin-Sandrow Syndrome Legius Syndrome Lower Lip Cancer Luteoma Lynch Syndrome Lynch Syndrome I Mismatch Repair Cancer Syndrome Muenke Syndrome Muir-Torre Syndrome Neurofibromatosis, Familial Spinal Neurofibromatosis, Type Iv, of Riccardi Neurofibrosarcoma Osteoglophonic Dysplasia Plagiocephaly Plexiform Neurofibroma Polycystic Kidney Disease 3 Polydactyly of a Triphalangeal Thumb, Bilateral Polydactyly of a Triphalangeal Thumb, Unilateral Polydactyly, Preaxial Ii Polyneuropathy Porphyria Radial Hemimelia, Bilateral Radial Hemimelia, Unilateral Retinitis Retinitis Pigmentosa Saethre-Chotzen Syndrome Sebaceous Adenocarcinoma Sebaceous Adenoma Skin Benign Neoplasm Small Intestine Cancer Spinal Cord Ependymoma Subclavian Artery Aneurysm Syndactyly, Type Iv Synostosis Tibia, Hypoplasia or Aplasia of, with Polydactyly
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