3417
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C9orf72-SMCR8 complex subunit |
ALSFTD, DENND9, DENNL72, FTDALS, FTDALS1 |
Curated: Amyotrophic lateral sclerosis, Juvenile arthritis, Autism, Eye disorder, Eye disease, Frontotemporal dementia, Frontotemporal dementia with or without amyotrophic lateral sclerosis, Frontotemporal dementia with motor neuron disease, Huntington disease, Juvenile idiopathic arthritis, Non-organic psychosis, Oligoarticular juvenile idiopathic arthritis, Progressive myoclonic epilepsy, Psychotic disorders, Schizoaffective disorder, Schizophrenia, frontotemporal dementia and/or amyotrophic lateral sclerosis 1
Unreviewed: Abulia, Alexia, Alzheimer disease, Amnesia, Amyotrophic Lateral Sclerosis, Amyotrophic Lateral Sclerosis With Dementia, Amyotrophy, Anomia, Anorexia, Anosmia, Anxiety Disorder, Aphasia, Apraxia, Arthritis, Asthma, Ataxia, Atrophy, Attention Deficit Hyperactivity Disorder, Auditory perceptual disorder, Autoimmune Diseases, Basal ganglia disease, Behavioral Variant Of Frontotemporal Dementia, Bipolar Disorder, Brain atrophy, Brain disease, Broca Aphasia, Bronchopneumonia, Bulbar palsy, Bulbospinal Atrophy, X-Linked, Bulimia, Bullous Pemphigoid, C9 deficiency, Calcium metabolism disorders, Cerebellar Ataxia, Cerebellar atrophy, Cerebellar Diseases, Cerebral Atrophy, Chorea, Cognition disorder, Cognitive disorder, Compulsive Hoarding, Cone-rod dystrophy, Corneal dystrophy, Cortical development malformation, Corticobasal Degeneration, Delusions, Dementia, Dermatopathia Pigmentosa Reticularis, Deuteranomaly, Developmental disability, Disorders of sex development, Dysarthria, Dyscalculia, Dysgraphia, Dyskinetic Syndrome, Dyslexia, Dysphagia, Dysphasia, Dystonia, Eating Disorders, Epilepsy, Essential tremor, Extrapyramidal dyskinesia, Extravasation of diagnostic and therapeutic materials, Fragile X Syndrome, Frontotemporal cerebral atrophy, Frontotemporal Dementia With Motor Neuron Disease, Ganglioneuroma, Grammar-specific speech disorder, Hallucinations, Hearing loss, Heart failure, Henoch-Schonlein Nephritis, Hepatic adenoma, Hepatitis b, Hepatocellular carcinoma, Huntington Disease, Huntington Disease-Like, Immune system disease, Immune System Diseases, Impaired Cognition, Intellectual developmental disorder, Language development disorders, Laryngospasm, Lateral Sclerosis, Lewy Body Disease, Liver disease, Liver neoplasm, Lymphoproliferative syndrome, Major depressive disorder, Malignant Neoplasm, Melanoma, Memory disorders, Mental Depression, Mental Disorders, Mental retardation, Mitochondrial disease, Mood Disorder, Mood swings, Motor neuron atrophy, Motor Neuron Disease, Movement disorder, Movement Disorders, Multiple polyposis syndrome, Multiple Sclerosis, Multiple system atrophy, Myasthenic syndrome, Myocardial infarction, Myositis, Myotonic dystrophy, Nephropathy with Pretibial Epidermolysis Bullosa and Deafness, Nervous System Disorder, Neuroblastoma, Neurodegenerative disorder, Neurodegenerative Disorders, Neurogenic Urinary Bladder, Neuromuscular disease, Neuronal ceroid lipofuscinosis, Night blindness, congenital stationary, Nonfluent Aphasia, Nonorganic Psychosis, Obsessive-Compulsive Disorder, Oculocerebrorenal syndrome, Paget disease, Papillon-Lefevre Disease, Paranoia, Parietal foramina, Parkinson disease, Pica, Polyarthritis, Rheumatoid Factor Positive, Polycystic Lipomembranous Osteodysplasia With Sclerosing Leukoencephalopathy, Progressive Muscular Atrophy, Progressive Non-Fluent Aphasia, Progressive Supranuclear Palsy, Psychiatric disorders, Psychosis, Ptosis, Respiratory Failure, Respiratory system infectious disease, Restless Legs Syndrome, Rheumatoid arthritis, Schilder disease, Schizoaffective Disorder, Secondary parkinson disease, Seizure, Semantic Dementia, Senile Dementia, Senile Plaques, Sensorineural hearing loss, Seronegative polyarthritis, Skin abnormalities, Spastic Paraplegia, Spinal Muscular Atrophy, Spinocerebellar Ataxia, Stereotyped Behavior, Still Disease, Tauopathies, Temporal cortical atrophy, Temporal lobe epilepsy, Torsades de pointes, Tremor, Visual disorder, Willis-ekbom disease
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3418
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Chromosome 9 open reading frame 78 |
CSU2, HCA59, HSPC220, TLS1, bA409K20.3 |
Curated: N/A
Unreviewed: N/A
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