Informaţii despre

Nume Leber Congenital Amaurosis
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificari ICD10 Hereditary retinal dystrophy
Clasificare anatomică Malacards Boli ale ochiului; Boli neuronale
Boli din aceeaşi familie Leber Congenital Amaurosis 1; Leber Congenital Amaurosis 10; Leber Congenital Amaurosis 11; Leber Congenital Amaurosis 12; Leber Congenital Amaurosis 13; Leber Congenital Amaurosis 14; Leber Congenital Amaurosis 15; Leber Congenital Amaurosis 16; Leber Congenital Amaurosis 17; Leber Congenital Amaurosis 2; Leber Congenital Amaurosis 3; Leber Congenital Amaurosis 4; Leber Congenital Amaurosis 5; Leber Congenital Amaurosis 6; Leber Congenital Amaurosis 7; Leber Congenital Amaurosis 8; Leber Congenital Amaurosis 9

Vezi şi

Boli A-Z 3-Methylglutaconic Aciduria, Type Iii Ablepharon-Macrostomia Syndrome Achromatopsia Achromatopsia 2 Achromatopsia 3 Achromatopsia 4 Adult Xanthogranuloma Aging Aleukemic Leukemia Cutis Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Aniridia 1 Anorexia Nervosa 1 Arthrochalasia Ehlers-Danlos Syndrome Atp8b1 Deficiency Autosomal Recessive Congenital Ichthyosis Bile Duct Disease Biliary Tract Disease Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Blue Cone Monochromacy Cancer-Associated Retinopathy Cataract Cerebrotendinous Xanthomatosis Cholestasis Choroidal Dystrophy, Central Areolar, 1 Choroideremia Choroiditis Color Blindness Cone Dystrophy Cone-Rod Dystrophy 2 Cone-Rod Dystrophy 6 Congenital Epulis Congenital Granular Cell Tumor Congenital Stationary Night Blindness Conventional Fibrosarcoma Cowden Syndrome 1 Degeneration of Macula and Posterior Pole Diffuse Meningeal Melanocytosis Down Syndrome Enhanced S-Cone Syndrome Ewing Sarcoma Extracutaneous Mastocytoma Extraosseous Osteosarcoma Eye Degenerative Disease Feingold Syndrome 1 Fundus Albipunctatus Fundus Dystrophy Gastric Small Cell Carcinoma Glomeruloid Hemangioma Granular Cell Tumor Granulomatous Myositis Hemangioma of Intra-Abdominal Structure Hemangioma of Liver Hepatic Adenomas, Familial Hepatitis Hereditary Choroidal Atrophy Hereditary Retinal Dystrophy Hodgkin's Lymphoma, Lymphocytic Depletion Hodgkin's Lymphoma, Mixed Cellularity Ichthyosis Keratoconus Leber Congenital Amaurosis 1 Leber Congenital Amaurosis 10 Leber Congenital Amaurosis 12 Leber Congenital Amaurosis 14 Leber Congenital Amaurosis 16 Leber Congenital Amaurosis 2 Leber Congenital Amaurosis 3 Leber Congenital Amaurosis 4 Leber Congenital Amaurosis 5 Leber Congenital Amaurosis 6 Leber Congenital Amaurosis 8 Leber Congenital Amaurosis 9 Leber Hereditary Optic Neuropathy Lichen Nitidus Liver Inflammatory Pseudotumor Lung Meningioma Lymphatic System Cancer Macular Degeneration, Age-Related, 1 Macular Dystrophy, Dominant Cystoid Macular Dystrophy, Vitelliform, 3 Macular Retinal Edema Malignant Epithelial Mesothelioma Malignant Giant Cell Tumor of Soft Parts Melanotic Neurilemmoma Metabolic Acidosis Multiple Mucosal Neuroma Nephronophthisis Neuropathy Night Blindness Nodular Tenosynovitis Oligocone Trichromacy Optic Nerve Disease Ovarian Solid Teratoma Partial Central Choroid Dystrophy Peripheral Retinal Degeneration Prolonged Electroretinal Response Suppression Ptosis Red-Green Color Blindness Reticulohistiocytic Granuloma Retinal Aplasia Retinal Degeneration Retinal Disease Retina Lymphoma Retinitis Retinitis Pigmentosa Retinitis Pigmentosa 1 Retinitis Pigmentosa 10 Retinitis Pigmentosa 26 Retinitis Pigmentosa 3 Retinitis Pigmentosa 43 Retinitis Pigmentosa 44 Retinitis Pigmentosa 7 Retinoschisis 1, X-Linked, Juvenile Rhinoscleroma Rhyns Syndrome Sarcomatoid Squamous Cell Skin Carcinoma Senior-Løken Syndrome Senior-Loken Syndrome 1 Severe Early-Childhood-Onset Retinal Dystrophy Small Cell Carcinoma Stargardt Disease Stargardt Disease 1 Stargardt Macular Degeneration Sternum Cancer Testicular Infarct Trichohepatoenteric Syndrome 1 Usher Syndrome Usher Syndrome, Type I Usher Syndrome, Type Iic Usher Syndrome, Type Iid Verruciform Xanthoma of Skin Xanthomatosis Yemenite Deaf-Blind Hypopigmentation Syndrome