Informaţii despre

Nume Alport Syndrome, X-Linked
Pagina Web
Clasificare globală Malacards Fetal diseases; Genetic diseases; Rare diseases
Clasificari ICD10 Other specified congenital malformation syndromes, not elsewhere classified
Clasificare anatomică Malacards Ear diseases; Eye diseases; Nephrological diseases

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Boli A-Z Ablepharon-Macrostomia Syndrome Acrocallosal Syndrome Aging Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome and Thin Basement Membrane Nephropathy Alport Syndrome, Autosomal Dominant Alport Syndrome, Autosomal Recessive Alport Syndrome-Intellectual Disability-Midface Hypoplasia-Elliptocytosis Syndrome Al-Raqad Syndrome Andersen Cardiodysrhythmic Periodic Paralysis Aniridia 1 Anorexia Nervosa 1 Arterial Tortuosity Syndrome Arteriolosclerosis Arthrochalasia Ehlers-Danlos Syndrome Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, I System Branchiootic Syndrome 1 Cataract Choroiditis Cole Disease Collagen Disease Congenital Syphilis Corneal Dystrophy Corneal Dystrophy, Posterior Polymorphous, 3 Coronary Artery Dissection, Spontaneous Craniopharyngioma Danubian Endemic Familial Nephropathy End Stage Renal Failure Epstein Syndrome Fanconi Anemia, Complementation Group E Fechtner Syndrome Focal Segmental Glomerulosclerosis Frasier Syndrome Gingivitis Glomerulonephritis Goodpasture Syndrome Hematuria, Benign Familial Hemorrhagic Fever Hemorrhagic Fever with Renal Syndrome Hepatic Adenomas, Familial Herpes Simplex Herpes Simplex Virus Keratitis Hydrocephalus Due to Congenital Stenosis of Aqueduct of Sylvius Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hypotonia Kidney Disease Leiomyomatosis Leiomyomatosis, Diffuse, with Alport Syndrome Lutheran Suppressor, X-Linked Macular Holes Malignant Cylindroma Membranoproliferative Glomerulonephritis Membranous Nephropathy Myh9 Related Thrombocytopenia Neurofibromatosis, Type I Neurofibromatosis, Type Iv, of Riccardi Orthostatic Proteinuria Periodontitis Peritonitis Polycystic Kidney Disease Pyelitis Pyelonephritis Renal Fibrosis Retinal Detachment Retinitis Sensorineural Hearing Loss Smooth Muscle Tumor Tetraamelia Syndrome, Autosomal Recessive Thalassemia Urinary System Disease Vasculitis Ventricular Septal Defect Vitreoretinal Degeneration X-Linked Diffuse Leiomyomatosis-Alport Syndrome