951
|
|
|
Sulfotransferase family 2A member 1 |
DHEA-ST, DHEA-ST8, DHEAS, HST, ST2, ST2A1, ST2A3, STD, SULT2A3, hSTa |
|
952
|
|
|
Suv3 like RNA helicase |
SUV3 |
|
953
|
|
|
SURF1 cytochrome c oxidase assembly factor |
CMT4K, MC4DN1, SHY1 |
Acquired kyphoscoliosis, Anemia, Breast cancer, Cardiomyopathy, Central nervous system demyelination, Cerebellar ataxia, Charcot-marie-tooth disease, Congenital kyphoscoliosis, Congestive heart failure, Cytochrome-c oxidase deficiency, Developmental delay, Developmental regression, Dysarthria, Dyskinetic syndrome, Dysmorphic features, Dysphagia, Encephalopathy, Hearing loss, Horizontal nystagmus, Hypertrichosis, Hypertrophic cardiomyopathy, Mental retardation, Leigh syndrome, Leigh syndrome with cardiomyopathy, Leigh syndrome with leukodystrophy, Leukodystrophy, Mitochondrial diseases, Mood swings, Movement disorders, Necrotizing encephalomyelopathy, Nervous system diseases, Nystagmus, Optic atrophy, Ptosis, Pulmonary stenosis, Renal agenesis, Renal dysplasia, Respiratory failure, Retinal diseases, Retinitis pigmentosa, Strabismus, Ventricular septal defectView all (27 more) |
954
|
|
|
Surfeit 4 |
ERV29 |
|
955
|
|
|
Supervillin |
MFM10 |
|
956
|
|
|
Synaptonemal complex protein 1 |
CT8, HOM-TES-14, SCP-1, SCP1 |
|
957
|
|
|
Spleen associated tyrosine kinase |
IMD82, p72-Syk |
|
958
|
|
|
Synapsin I |
EPILX, EPILX1, MRX50, SYN1a, SYN1b, SYNI |
|
959
|
|
|
Synapsin II |
SYNII |
|
960
|
|
|
Synaptophysin |
MRX96, MRXSYP, XLID96 |
Attention deficit hyperactivity disorder, Autism, Developmental delay, Facial paralysis, Neurosensory hearing impairment, Mental retardation, Learning disorders, Lung carcinoma, Macrocephaly, Meckel diverticulum, Memory disorders, Age-related memory disorders, Mental retardation, x-linked, Neuronal ceroid lipofuscinosis, Non-syndromic intellectual disability, x-linked, Obesity, Schizophrenia, Seizure, Syndactyly of the toesView all (4 more) |