Informaţii despre

Nume Apraxia
Pagina Web www.malacards.org
Clasificare globală Malacards Boli rare
Clasificari ICD10 Apraxia
Clasificare anatomică Malacards Boli psihice

Vezi şi

Boli A-Z Adie Pupil Aging Agnosia Agraphia Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha-Fetoprotein Deficiency Al-Raqad Syndrome Amyotrophic Lateral Sclerosis 21 Analbuminemia Androgen Insensitivity Syndrome, Mild Aniridia 1 Anorexia Nervosa 1 Anosognosia Anterior Cerebral Artery Infarction Aphasia Apraxia of Eyelid Opening Arachnoid Cysts Arachnoiditis Arthrochalasia Ehlers-Danlos Syndrome Articulation Disorder Ataxia and Polyneuropathy, Adult-Onset Ataxia, Early-Onset, with Oculomotor Apraxia and Hypoalbuminemia Ataxia-Oculomotor Apraxia 3 Ataxia-Oculomotor Apraxia 4 Ataxia-Telangiectasia Autism Autism Spectrum Disorder Autosomal Recessive Cerebellar Ataxia Axonal Neuropathy Basal Ganglia Disease Behavioral Variant of Frontotemporal Dementia Bleeding Disorder, Platelet-Type, 11 Blepharospasm Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Brain Injury Cerebellar Disease Cerebral Degeneration Cerebritis Cerebrovascular Disease Cervical Dystonia Cervicitis Childhood Apraxia of Speech Communicating Hydrocephalus Congenital Contractures Corticobasal Degeneration Creutzfeldt-Jakob Disease Cri-Du-Chat Syndrome Dementia Developmental Dyspraxia Dilated Cardiomyopathy Down Syndrome Duane Retraction Syndrome 1 Dysgraphia Dyslexia Dysphasia, Familial Developmental Dystonia Encephalitis Epilepsy Essential Tremor Fanconi Anemia, Complementation Group E Foxp2-Related Speech and Language Disorders Frontotemporal Dementia Frontotemporal Lobar Degeneration with Tdp43 Inclusions, Grn-Related Gait Apraxia Galactosemia Headache Hemiplegia Hepatic Adenomas, Familial Hydrocephalus Hyperparathyroidism Hypotonia Ideomotor Apraxia Japanese Encephalitis Joubert Syndrome with Ocular Anomalies Kleefstra Syndrome Lateral Sclerosis Lipoid Proteinosis of Urbach and Wiethe Loeys-Dietz Syndrome 3 Lymphoid Interstitial Pneumonia Macs Syndrome Mast Cell Activation Syndrome Meckel Syndrome, Type 1 Microcephaly Motor Neuron Disease Multiple Acyl-Coa Dehydrogenase Deficiency Multiple Sclerosis Multiple System Atrophy 1 Mutism Myotonia Nephronophthisis Neurodegeneration with Brain Iron Accumulation 2a Neuromyelitis Optica Neuromyelitis Optica Spectrum Disorder Neuronal Ceroid Lipofuscinosis Neuronitis Neuropathy Nominal Aphasia Ocular Motor Apraxia Parkinson-Dementia Syndrome Pedophilia Pervasive Developmental Disorder Pharyngitis Primary Progressive Apraxia of Speech Progressive Non-Fluent Aphasia Ptosis Pyruvate Carboxylase Deficiency Segmental Dystonia Semantic Dementia Simultanagnosia Sleep Apnea Spasmus Nutans Spastic Ataxia, Charlevoix-Saguenay Type Specific Language Impairment Speech and Communication Disorders Speech Disorder Spinal Cord Injury Spinocerebellar Ataxia, Autosomal Recessive 1 Spinocerebellar Ataxia with Axonal Neuropathy Type 2 Stiff-Person Syndrome Stuttering Sveinsson Chorioretinal Atrophy Takayasu Arteritis Traumatic Brain Injury Tremor Vascular Dementia Velocardiofacial Syndrome Visual Agnosia