Informaţii despre

Nume Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificari ICD10 Multi-infarct dementia
Clasificare anatomică Malacards Boli ale ochiului; Boli cardiovasculare; Boli de piele; Boli neuronale; Boli psihice
Boli din aceeaşi familie Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 2

Vezi şi

Boli A-Z Adams-Oliver Syndrome Aging Alagille Syndrome 1 Aland Island Eye Disease Alopecia Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alport Syndrome, X-Linked Al-Raqad Syndrome Amyloidosis Androgen Insensitivity Syndrome, Mild Aneurysm Aniridia 1 Anorexia Nervosa 1 Arteries, Anomalies of Arteriovenous Malformation Arthrochalasia Ehlers-Danlos Syndrome Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Ataxia Neuropathy Spectrum Atypical Choroid Plexus Papilloma Balo Concentric Sclerosis Binswanger's Disease Bipolar Disorder Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Blood Group--Kidd System Brain Small Vessel Disease with or Without Ocular Anomalies Central Nervous System Origin Vertigo Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 2 Cerebral Arteriopathy, Autosomal Recessive, with Subcortical Infarcts and Leukoencephalopathy Cerebral Hemorrhage Cerebritis Cerebroretinal Microangiopathy with Calcifications and Cysts 1 Cerebrovascular Disease Cervicitis Chorioretinal Scar Complement Factor B Deficiency Dementia Encephalopathy Endotheliitis Epilepsy Fabry Disease Factor Xii Deficiency Familial Hemiplegic Migraine Fetal Akinesia Deformation Sequence Focal Epilepsy Frontotemporal Dementia Hajdu-Cheney Syndrome Headache Hemiplegia Hemiplegic Migraine Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertensive Retinopathy Ischemia Ischemic Retinopathy Lateral Sclerosis Lung Adenoma Migraine with Aura Mood Disorder Multiple Sclerosis Multiple System Atrophy 1 Myocardial Infarction Myopathy Neuronitis Neuropathy Nodular Regenerative Hyperplasia Ocular Motor Apraxia Ossifying Fibroma Papillomatosis, Confluent and Reticulated Parametritis Pathological Gambling Periodontal Disease Periodontitis Peripheral Artery Disease Primary Angiitis of the Central Nervous System Pseudobulbar Palsy Retinitis Salt and Pepper Developmental Regression Syndrome Schizophrenia Sensorineural Hearing Loss Siderosis Spinal Cord Infarction Split-Hand/foot Malformation 1 Sporadic Hemiplegic Migraine Status Epilepticus Subcortical Arteriosclerotic Encephalopathy Sudden Sensorineural Hearing Loss Superficial Siderosis Thrombocytopenia Thrombocytopenia Due to Platelet Alloimmunization Transient Global Amnesia Varicose Veins Vascular Dementia Vascular Disease