| SLC6A8 | |
| Gene ID | 6535 |
| Gene Symbol | SLC6A8 |
| Gene Name | solute carrier family 6 (neurotransmitter transporter, creatine), member 8 |
| Organism | human |
| Phenotype from JST bibliography | Mental Retardation, X-Linked (MeSH); X-linked mental retardation; X連鎖精神発達遅滞; non-syndromic X-linked mental retardation; 精神発達遅滞 |
| MeSH Tree | Nervous System Diseases > Neurologic Manifestations > Neurobehavioral Manifestations > Mental Retardation > Mental Retardation, X-Linked Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Genetic Diseases, X-Linked > Mental Retardation, X-Linked Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Heredodegenerative Disorders, Nervous System > Mental Retardation, X-Linked |
| MeSH Tree (日本語) | 神経系疾患 > 神経症状 > 神経行動症状 > 精神遅滞 > X染色体連鎖精神発達障害 先天性疾患、遺伝病、新生児疾患、奇形 > 遺伝病 > X染色体連鎖遺伝病 > X染色体連鎖精神発達障害 先天性疾患、遺伝病、新生児疾患、奇形 > 遺伝病 > 神経系遺伝性変性疾患 > X染色体連鎖精神発達障害 |
| JST bibliography database | 05A0569335 |