Informaţii despre

Nume Albinism
Pagina Web www.malacards.org
Clasificare globală Malacards Boli metabolice; Boli rare
Clasificari ICD10 Albinism

Vezi şi

Boli A-Z Abcd Syndrome Actinic Cheilitis Actinic Keratosis Aging Aland Island Eye Disease Albinism-Deafness Syndrome Albinism Immunodeficiency Albinism, Ocular, Type I Albinism, Ocular, with Late-Onset Sensorineural Deafness Albinism, Ocular, with Sensorineural Deafness Albinism, Oculocutaneous, Type Ia Albinism, Oculocutaneous, Type Ib Albinism, Oculocutaneous, Type Ii Albinism, Oculocutaneous, Type Iii Albinism, Oculocutaneous, Type Iv Albinism, Oculocutaneous, Type V Albinism, Oculocutaneous, Type Vi Alkaptonuria Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha-Methylacyl-Coa Racemase Deficiency Alport Syndrome, X-Linked Al-Raqad Syndrome Amelanotic Melanoma Amelogenesis Imperfecta Aneurysm Aneurysm of Sinus of Valsalva Angelman Syndrome Aniridia 1 Anorexia Nervosa 1 Arthrochalasia Ehlers-Danlos Syndrome Ataxia and Polyneuropathy, Adult-Onset Ataxia-Oculomotor Apraxia 3 Attention Deficit-Hyperactivity Disorder Audiogenic Seizures Autism Ayme-Gripp Syndrome Basal Cell Carcinoma Bipolar Disorder Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Branchiootic Syndrome 1 Burns Cataract Chediak-Higashi Syndrome Cheilitis Chondrodysplasia Punctata Syndrome Choroiditis Colitis Coloboma, Osteopetrosis, Microphthalmia, Macrocephaly, Albinism, and Deafness Color Blindness Colorblindness, Partial, Protan Series Complement Component 6 Deficiency Congenital Ichthyosiform Erythroderma Congenital Nystagmus Crest Syndrome Cryptophthalmos Cyclic Neutropenia Cyclic Vomiting Syndrome Cystinuria Diabetes Mellitus Dilution, Pigmentary Dowling-Degos Disease 1 Duane Retraction Syndrome Dyschromatosis Symmetrica Hereditaria Dyskeratosis Congenita Dysplastic Nevus Syndrome Ectropion Epithelial Recurrent Erosion Dystrophy Epithelioid Cell Melanoma Esotropia Glutathione Synthetase Deficiency Glycerol Kinase Deficiency Griscelli Syndrome Hansen's Disease Hemolytic Anemia Hemophagocytic Lymphohistiocytosis Hemophilia Hemophilia B Hermansky-Pudlak Syndrome Hermansky-Pudlak Syndrome 1 Hermansky-Pudlak Syndrome 3 Hermansky-Pudlak Syndrome 4 Hermansky-Pudlak Syndrome with Pulmonary Fibrosis Human Coronavirus Sensitivity Hydrocephalus Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hypoadrenocorticism, Familial Hypomelanotic Disorder Ichthyosis Isolated Duane Retraction Syndrome Kallmann Syndrome Keloids Keratoconjunctivitis Keratoconjunctivitis Sicca Keratoconus Keratosis Knobloch Syndrome Kotzot-Richter Syndrome Laryngeal Cleft Linear Skin Defects with Multiple Congenital Anomalies 1 Malignant Spindle Cell Melanoma Maple Syrup Urine Disease Marcus Gunn Phenomenon Megalocornea Melanoma Meningitis Menkes Disease Metabolic Acidosis Microphthalmia Motor Neuron Disease Multiple Sulfatase Deficiency Muscular Dystrophy Mutism Neuritis Neurofibroma Neuronitis Neutropenia Ocular Albinism Ocular Albinism, X-Linked Oculocutaneous Albinism Optic Neuritis Osteopetrosis Pancreatitis, Hereditary Pentosuria Periodontal Disease Periodontitis Piebald Trait Pigmented Basal Cell Carcinoma Plexiform Neurofibroma Prader-Willi Syndrome Pulmonary Fibrosis Refractive Error Retinal Degeneration Retinal Detachment Retinitis Retinitis Pigmentosa Schizophrenia Sickle Cell Disease Skin/hair/eye Pigmentation, Variation in, 3 Spastic Ataxia, Charlevoix-Saguenay Type Spondyloocular Syndrome Squamous Cell Carcinoma Storage Pool Platelet Disease Strabismus Supravalvular Aortic Stenosis Tetraamelia Syndrome, Autosomal Recessive Tièche-Jadassohn Nevus Tietz Albinism-Deafness Syndrome Trichomegaly Tyrosinase-Like Vici Syndrome Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 Waardenburg's Syndrome Waardenburg Syndrome, Type 2e