Informaţii despre

Nume Fabry Disease
Pagina Web www.malacards.org
Clasificare globală Malacards Fetal diseases; Genetic diseases; Metabolic diseases; Rare diseases
Clasificari ICD10 Other sphingolipidosis
Clasificare anatomică Malacards Eye diseases; Nephrological diseases; Neuronal diseases; Skin diseases

Vezi şi

Boli A-Z 3-Hydroxyacyl-Coa Dehydrogenase Deficiency Acrocallosal Syndrome Adie Pupil Aganglionosis, Total Intestinal Aging Alopecia, Androgenetic, 1 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Al-Raqad Syndrome Amyloidosis Aneurysm Angioedema Angiokeratoma Angiokeratoma of Fordyce Anhidrosis Aniridia 1 Anorexia Nervosa 1 Arthrochalasia Ehlers-Danlos Syndrome Aseptic Meningitis Aspartylglucosaminuria Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Ataxia Neuropathy Spectrum Atrial Fibrillation Atrioventricular Block Autonomic Neuropathy Azoospermia Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Burns Carpal Tunnel Syndrome Central Retinal Artery Occlusion Cerebral Hemorrhage Cerebritis Cerebrovascular Disease Cheilitis Cholestasis-Lymphedema Syndrome Chronic Meningitis Cleft Larynx, Posterior Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Corneal Deposit Cramp-Fasciculation Syndrome Cutaneous Polyarteritis Nodosa Cutis Laxa, Autosomal Recessive, Type Iiia Cystinosis Danon Disease Diabetes Insipidus Diffuse Lymphatic Malformation Ectodermal Dysplasia Encephalopathy Endocarditis Endotheliitis End Stage Renal Failure Erythermalgia, Primary Erythromelalgia Exocrine Pancreatic Insufficiency Familial Mediterranean Fever Fanconi Anemia, Complementation Group E Farber Lipogranulomatosis First-Degree Atrioventricular Block Fucosidosis Gingivitis Glossitis Glycogen Storage Disease Ii Glycogen Storage Disease Vi Glycoproteinosis Guillain-Barre Syndrome, Familial Hashimoto Thyroiditis Hepatic Adenomas, Familial Hereditary Angioedema Hypersplenism Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertensive Heart Disease Hypertrophic Cardiomyopathy Hypohidrosis Ichthyosis Prematurity Syndrome Ileitis Immunoglobulin E Concentration, Serum Incontinentia Pigmenti Inherited Metabolic Disorder Keratopathy Lactic Acidosis Lateral Sclerosis Left Ventricular Noncompaction Lipid Storage Disease Lupus Erythematosus Lymphoma Meningitis Migraine with Aura Mitochondrial Myopathy Mononeuropathy of the Median Nerve, Mild Mucolipidosis Iv Mucopolysaccharidosis-Plus Syndrome Multiple Sclerosis Myoclonic Epilepsy, Familial Infantile Myopathy Neuronitis Neuropathy Neuropathy, Hereditary Sensory and Autonomic, Type Iii Nondisjunction Otosclerosis Pancreatitis Phenylketonuria Polyarteritis Nodosa Priapism Purpura Refsum Disease, Classic Renal Artery Atheroma Retinal Artery Occlusion Retinitis Retinoschisis 1, X-Linked, Juvenile Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Skin Hemangioma Sphingolipidosis Splenomegaly Spondyloocular Syndrome Syringomyelia Systemic Lupus Erythematosus Tay-Sachs Disease T Cell Deficiency Tetrahydrobiopterin Deficiency Thrombosis Thyroiditis Turner Syndrome Undifferentiated Pleomorphic Sarcoma Vascular Disease Vitamin E, Familial Isolated Deficiency of Weber Syndrome