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Informaţii despre
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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