Informaţii despre

Nume Cerebral Amyloid Angiopathy, Cst3-Related
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli metabolice; Boli rare
Clasificari ICD10 Cerebral amyloid angiopathy
Clasificare anatomică Malacards Boli cardiovasculare; Boli neuronale; Boli osoase

Vezi şi

Boli A-Z Aganglionosis, Total Intestinal Aging Agraphia Akinetic Mutism Aland Island Eye Disease Alexia Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Al-Raqad Syndrome Alzheimer Disease Alzheimer Disease 2 Alzheimer Disease 3 Alzheimer Disease 4 Alzheimer Disease Mitochondrial Amyloidosis Amyloidosis, Finnish Type Anauxetic Dysplasia 1 Aniridia 1 Anorexia Nervosa 1 Aphasia Apnea, Obstructive Sleep Arteriosclerosis Arthrochalasia Ehlers-Danlos Syndrome Atrial Fibrillation Aural Atresia, Congenital B-Cell Lymphomas Behavioral Variant of Frontotemporal Dementia Benign Meningioma Binswanger's Disease Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Body Mass Index Quantitative Trait Locus 10 Body Mass Index Quantitative Trait Locus 11 Body Mass Index Quantitative Trait Locus 12 Body Mass Index Quantitative Trait Locus 14 Body Mass Index Quantitative Trait Locus 18 Body Mass Index Quantitative Trait Locus 4 Body Mass Index Quantitative Trait Locus 7 Body Mass Index Quantitative Trait Locus 8 Body Mass Index Quantitative Trait Locus 9 Brain Injury Breast Cancer Central Nervous System Disease Central Nervous System Vasculitis Cerebral Amyloid Angiopathy, Itm2b-Related, 1 Cerebral Amyloid Angiopathy, Itm2b-Related, 2 Cerebral Artery Occlusion Cerebral Hemorrhage Cerebritis Cerebrovascular Disease Childhood Disintegrative Disease Choroiditis Communicating Hydrocephalus Creutzfeldt-Jakob Disease Dementia Dementia, Lewy Body Dementia Pugilistica Down Syndrome Early-Onset, Autosomal Dominant Alzheimer Disease Early-Onset Familial Alzheimer Disease Encephalopathy Endotheliitis Factor Xiii Deficiency Familial Idiopathic Basal Ganglia Calcification Farber Lipogranulomatosis Frontotemporal Dementia Gait Apraxia Genetic Prion Diseases Gerstmann-Straussler Disease Granulomatous Angiitis Head Injury Hemorrhage, Intracerebral Hemosiderosis Hepatic Adenomas, Familial Hereditary Cerebral Amyloid Angiopathy Hydrocephalus, Normal-Pressure Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypoxia Ichthyosis Vulgaris Inclusion Body Myositis Intravascular Large B-Cell Lymphoma Ischemia Kluver-Bucy Syndrome Leukoencephalopathy, Hereditary Diffuse, with Spheroids Lymphoma Meningitis Migraine with or Without Aura 1 Motor Neuron Disease Nervous System Disease Neuronitis Paresthesia Parkinson Disease 15, Autosomal Recessive Early-Onset Pick Disease of Brain Polyneuropathy Posterior Cortical Atrophy Primary Angiitis of the Central Nervous System Prion Disease Progressive Non-Fluent Aphasia Prosopagnosia Retinitis Rheumatoid Vasculitis Salt and Pepper Developmental Regression Syndrome Scoliosis, Isolated 1 Semantic Dementia Senile Plaque Formation Siderosis Speech and Communication Disorders Status Epilepticus Subcortical Arteriosclerotic Encephalopathy Superficial Siderosis Supranuclear Palsy, Progressive, 1 Toxic Encephalopathy Traumatic Brain Injury Treacher Collins Syndrome 1 Undifferentiated Pleomorphic Sarcoma Vascular Dementia Vascular Disease Vasculitis