Informaţii despre

Nume Rett Syndrome
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificari ICD10 Rett syndrome
Clasificare anatomică Malacards Boli neuronale; Boli psihice
Boli din aceeaşi familie Rett Syndrome, Congenital Variant

Vezi şi

Boli A-Z 14q12 Microdeletion Syndrome Adie Pupil Aging Alacrima, Achalasia, and Mental Retardation Syndrome Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Amnestic Disorder Angelman Syndrome Aniridia 1 Anorexia Nervosa 1 Anoxia Apocrine Gland Secretion, Variation in Arthrochalasia Ehlers-Danlos Syndrome Aspiration Pneumonia Ataxia and Polyneuropathy, Adult-Onset Ataxia Neuropathy Spectrum Attention Deficit-Hyperactivity Disorder Autism Autism Spectrum Disorder Autonomic Dysfunction Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Bone Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Bornholm Eye Disease Bruxism Cardiac Arrhythmia Cdkl5-Related Disorder Cerebellar Atrophy, Developmental Delay, and Seizures Cerebritis Christianson Syndrome Chromosomal Triplication Chromosome 16p13.3 Deletion Syndrome, Proximal Constipation Cowden Syndrome 1 Dementia Diabetes Mellitus Distal Chromosome 18q Deletion Syndrome Down Syndrome Dysautonomia Dysphagia Dystonia Encephalopathy Epilepsy Epileptic Encephalopathy, Early Infantile, 2 Fanconi Anemia, Complementation Group E Fetal Alcohol Syndrome Gallbladder Disease Gilles De La Tourette Syndrome Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies Glycogen Storage Disease Vi Hepatic Adenomas, Familial Hypotonia Hypoxia Ichthyosis Prematurity Syndrome Infantile Hypotonia Intellectual Disability-Developmental Delay-Contractures Syndrome Krabbe Disease Leukemia Lung Disease Marchiafava Bignami Disease Mecp2-Related Disorders Microcephaly Muscular Atrophy Myoclonus Neurofibromatosis, Type Iv, of Riccardi Neuronal Ceroid Lipofuscinosis Neuronitis Ocular Dominance Pervasive Developmental Disorder Pneumonia Polykaryocytosis Inducer Precocious Puberty Radin Blood Group Antigen Renal Tubular Acidosis Restrictive Dermopathy, Lethal Reticular Dysgenesis Salt and Pepper Developmental Regression Syndrome Scoliosis Sleep Disorder Spasticity Spinal Cord Injury Spinal Muscular Atrophy Split-Hand/foot Malformation 1 with Sensorineural Hearing Loss, Autosomal Recessive Temporal Lobe Epilepsy Tracheoesophageal Fistula Tremor Tuberous Sclerosis