2961
|
|
|
SPEM family member 2 |
C17orf74 |
Curated: Asthma, Uterine fibroid
Unreviewed: N/A
|
2962
|
|
|
SPEM family member 3 |
- |
Curated: N/A
Unreviewed: N/A
|
2963
|
|
|
Spen family transcriptional repressor |
HIAA0929, MINT, RATARS, RBM15C, SHARP |
Curated: 1p36 deletion syndrome, Alzheimer disease, Atrial fibrillation, Autism, Neurodevelopmental disorder, Non-specific syndromic intellectual disability, Prostate cancer, Prostatic neoplasms, radio-tartaglia syndrome
Unreviewed: N/A
|
2964
|
|
|
SPEN antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
|
2965
|
|
|
Sperm equatorial segment protein 1 |
ESP, SP-ESP |
Curated: N/A
Unreviewed: Arthritis, Colitis, Congenital heart defect, Coronary Arteriosclerosis, Coronary artery disease, Coronary Heart Disease, Diabetes Mellitus, Kidney Disease, Kidney Failure, Leukemia, Malignant Neoplasm, Marfan Syndrome, Myocardial Infarction, Rheumatoid arthritis
|
2966
|
|
|
- |
- |
Curated: Obesity
Unreviewed: N/A
|
2967
|
|
|
SPG11 vesicle trafficking associated, spatacsin |
ALS5, CMT2X, KIAA1840 |
Curated: Alzheimer disease, Amyotrophic lateral sclerosis, Autism, Charcot-marie-tooth disease, Spastic paraplegia, Intellectual developmental disorder, Parkinson disease, Spastic ataxia, Hereditary spastic paraplegia, hereditary spastic paraplegia 11
Unreviewed: Age-related macular degeneration, Agenesis Of Corpus Callosum, Akinesia, Amyotrophic Lateral Sclerosis, Ataxia, Atrophy Of Corpus Callosum, Basal ganglia disease, Bipolar Disorder, Bowel incontinence, Brain disease, Cerebellar ataxia, Cerebellar diseases, Cerebral cortical atrophy, Charcot-Marie-Tooth Disease, Cholestanol storage disease, Cognition disorder, Cognitive disorder, Congenital cataract, Corpus callosum agenesis, Cortical development malformation, Deglutition disorder, Dementia, Developmental delay, Distal amyotrophy, Distal peripheral sensory neuropathy, Dysarthria, Dysphagia, Dysplastic corpus callosum, Dystonia, Epilepsy, Frontotemporal dementia, Gaucher disease, Genetic predisposition to disease, Graves ophthalmopathy, Heart disease, Henoch-Schonlein Nephritis, Hereditary sensory and motor neuropathy, Homocarnosinase Deficiency, Homocarnosinosis, Hypoplasia Of Corpus Callosum, Impaired Cognition, Learning disorders, Leukodystrophy, Lymphedema, Macular degeneration, Memory disorders, Mental Depression, Mental Disorders, Mental retardation, Mitochondrial disease, Motor neuron atrophy, Motor neuron disease, Movement disorder, Multiple Sclerosis, Nakamura Osame Syndrome, Nervous system disease, Nervous System Diseases, Neurodegenerative disorder, Neurodegenerative Disorders, Neuropathy, Nystagmus, Obesity, Ophthalmoplegia, Paraparesis, Paraplegia, Parkinson Disease, Parkinsonian disease, Peripheral axonal neuropathy, Peripheral nervous system disease, Peripheral Neuropathy, Polyneuropathy, Psychotic disorders, Schizophrenia, Secondary parkinson disease, Senile Dementia, Sensory neuropathy, Spastic Paraplegia, Specific Learning Disorder, Spinal muscular atrophy, Spinocerebellar ataxia, Spondylometaphyseal dysplasia, Tarsal-Carpal Coalition Syndrome, Troyer Syndrome
|
2968
|
|
|
- |
- |
Curated: N/A
Unreviewed: Intellectual developmental disorder, Paraplegia, Spastic Paraplegia, Spinal muscular atrophy
|
2969
|
|
|
- |
SPG |
Curated: N/A
Unreviewed: Gangrene, Henoch-Schonlein Nephritis, Hypoplasia Of Corpus Callosum, Neurodegenerative Disorders, Pelizaeus-Merzbacher disease, Scleroderma, Spastic Paraplegia, Spastic Paraplegia, X-Linked, Tarsal-Carpal Coalition Syndrome
|
2970
|
|
|
- |
- |
Curated: N/A
Unreviewed: Spastic paraplegia
|