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Nume Autosomal Genetic Disease
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Boli A-Z Acrofacial Dysostosis Actinic Cheilitis Adenoma Adenosquamous Colon Carcinoma Aging Alpha-Thalassemia Amyloid Tumor Anal Fistula Appendix Carcinoid Tumor Arthrochalasia Ehlers-Danlos Syndrome Astrocytoma Attenuated Familial Adenomatous Polyposis Atypical Polypoid Adenomyoma Atypical Werner Syndrome Autosomal Dominant Disease Autosomal Dominant Limb-Girdle Muscular Dystrophy Autosomal Dominant Polycystic Kidney Disease Bardet-Biedl Syndrome 17 Beta-Thalassemia Birt-Hogg-Dube Syndrome Brain Cancer Breast Papillary Carcinoma Calcifying Epithelial Odontogenic Tumor Caroli Disease Cecal Benign Neoplasm Cecum Adenocarcinoma Cell Type Benign Neoplasm Cellular Schwannoma Cerebral Aneurysms Cerebral Convexity Meningioma Cerebro-Oculo-Facio-Skeletal Syndrome Childhood Kidney Cell Carcinoma Choroid Plexus Cancer Cockayne Syndrome Cockayne Syndrome B Colonic Benign Neoplasm Colorectal Adenocarcinoma Colorectal Adenoma Colorectal Cancer Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly Congenital Hemolytic Anemia Congenital Hepatic Fibrosis Cowden Disease Cystic Fibrosis Cystic Kidney Disease Deafness, Autosomal Dominant 13 Deafness, Autosomal Dominant 6 Deafness, Autosomal Recessive 12 Deafness, Autosomal Recessive 16 Deafness, Autosomal Recessive 23 Deafness, Autosomal Recessive 4, with Enlarged Vestibular Aqueduct Diffuse Gastric Cancer Elephantiasis Endometrial Adenocarcinoma Endometrial Cancer Familial Adenomatous Polyposis Familial Colorectal Cancer Familial Renal Oncocytoma Familial Renal Papillary Carcinoma Female Reproductive Organ Cancer Fetal Hemoglobin Quantitative Trait Locus 1 Gastric Cancer Gastric Leiomyoma Gastrointestinal System Benign Neoplasm Gastrointestinal System Cancer Gliofibroma Hemoglobin C Disease Hemoglobin D Disease Hemoglobin E Disease Hemoglobin H Disease Hemoglobin Lepore-Beta-Thalassemia Syndrome Hemoglobinopathy Hepatic Adenomas, Familial Hereditary Breast Ovarian Cancer Syndrome Hereditary Persistence of Fetal Hemoglobin-Beta-Thalassemia Syndrome Hereditary Persistence of Fetal Hemoglobin-Sickle Cell Disease Syndrome Hereditary Renal Cell Carcinoma Hormone Producing Pituitary Cancer Hyperparathyroidism Hyperparathyroidism 2 with Jaw Tumors Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertension, Essential Hypophosphatemic Bone Disease Integumentary System Cancer Intestinal Benign Neoplasm Jejunal Cancer Keratoacanthoma Kidney Angiomyolipoma Kidney Cancer Legius Syndrome Li-Fraumeni Syndrome Lip Cancer Lipomatosis Lower Lip Cancer Lung Disease Lung Papillary Adenocarcinoma Lymphatic Malformations Lynch Syndrome Lynch Syndrome I Malignant Peripheral Nerve Sheath Tumor Malignant Secondary Hypertension Melanocytic Nevus Syndrome, Congenital Melanotic Neurilemmoma Meningioma, Radiation-Induced Mid-Dermal Elastolysis Mismatch Repair Cancer Syndrome Muir-Torre Syndrome Multiple Endocrine Neoplasia Multiple Endocrine Neoplasia Type 1 and Type 2 Multiple Endocrine Neoplasia, Type I Multiple Endocrine Neoplasia, Type Iia Multiple Endocrine Neoplasia, Type Iib Multiple Endocrine Neoplasia, Type Iv Multiple Self-Healing Squamous Epithelioma Mutagen Sensitivity Mutyh-Associated Polyposis Nervous System Cancer Neurilemmoma Neurilemmomatosis Neurofibromatosis, Familial Spinal Neurofibromatosis, Type Iv, of Riccardi Neurofibrosarcoma Olfactory Groove Meningioma Optic Nerve Neoplasm Organ System Benign Neoplasm Osgood-Schlatter's Disease Pancreatic Islet Cell Tumors Peutz-Jeghers Syndrome Pheochromocytoma Plexiform Neurofibroma Polycystic Kidney Disease Polycystic Kidney Disease 1 Polycystic Kidney Disease 2 Polycystic Kidney Disease 3 Polycystic Kidney Disease 4 with or Without Hepatic Disease Polycystic Kidney Disease 5 Polycystic Kidney Disease, Infantile Severe, with Tuberous Sclerosis Polycystic Liver Disease Polycystic Liver Disease 1 Polyposis Syndrome, Hereditary Mixed, 1 Primary Hyperparathyroidism Primary Peritoneal Carcinoma Pseudoxanthoma Elasticum Pten Hamartoma Tumor Syndrome Rectal Neoplasm Renal-Hepatic-Pancreatic Dysplasia Sebaceous Adenocarcinoma Sebaceous Adenoma Sensorineural Hearing Loss Sickle Cell Disease Skin Benign Neoplasm Small Intestine Cancer Spinal Cancer Spinal Cord Ependymoma Spinal Meningioma Sporadic Breast Cancer Thalassemia Thyroid Cancer, Nonmedullary, 1 Trichothiodystrophy 1, Photosensitive Tricuspid Valve Prolapse Tuberous Sclerosis Usher Syndrome, Type Id Von Hippel-Lindau Syndrome Xeroderma Pigmentosum, Complementation Group B Xeroderma Pigmentosum, Complementation Group D Xeroderma Pigmentosum, Complementation Group F Xeroderma Pigmentosum, Complementation Group G Xeroderma Pigmentosum, Variant Type Xfe Progeroid Syndrome