|
781
|
|
|
Solute carrier family 6 member 3 |
DAT, DAT1, PKDYS, PKDYS1 |
Anhedonia, Anxiety disorder, Attention deficit hyperactivity disorder, Bipolar disorder, Breast cancer, Cerebral palsy, Delirium, Dementia, Developmental delay, Dyskinetic syndrome, Dystonia-parkinsonism, Febrile seizures, Gastroesophageal reflux disease, Orofacial dyskinesia, Memory disorders, Age-related memory disorders, Mental depression, Mental depression with psychotic features, Mental retardation, Minimal brain dysfunction, Mood disorder, Motor tic disorders, Nervous system disorder, Paranoia, Parkinson disease, Parkinsonism-dystonia, Quadriplegia, Schizophrenia, Scoliosis, Senile paranoid dementia, Short sleeper syndromes, Sleep disorders, Sleep wake disorders, Spina bifida occulta, Tic disorder, Transient tic disorderView all (21 more) |
|
782
|
|
|
Solute carrier family 6 member 4 |
5-HTT, 5-HTTLPR, 5HTT, HTT, OCD1, SERT, SERT1, hSERT |
Affective psychosis, Anhedonia, Anxiety disorder, As if personality, Asperger syndrome, Autism, Bipolar disorder, Cognitive disorder, Compulsive hoarding, Dysthymic disorder, Impulse-ridden personality, Inadequate personality, Involutional depression, Involutional paraphrenia, Manic disorder, Melancholia, Memory disorders, Age-related memory disorders, Mental depression, Mood disorder, Obsessive-compulsive disorder, Personality disorders, Psychosis, Schizophrenia, Seasonal affective disorder, Skin-pickingView all (11 more) |
|
783
|
|
|
Solute carrier family 6 member 6 |
HTRDC, TAUT |
|
|
784
|
|
|
Solute carrier family 6 member 8 |
CCDS1, CRT, CRT-1, CRT1, CRTR, CT1, CTR5 |
Attention deficit hyperactivity disorder, Autism, Creatine deficiency, Creatine transporter deficiency, x-linked, Development disorder, Developmental delay, Dwarfism, Dysmorphic features, Exotropia, Hirschsprung disease, Hyperopia, Hypoplasia of corpus callosum, Ileus, Malocclusion, Mental retardation, Microcephaly, Motor delay, Hypotonia, Ptosis, Social communication disorder, Stereotyped behaviorView all (6 more) |
|
785
|
|
|
Surfactant protein A1 |
COLEC4, ILD1, PSAP, PSP-A, PSPA, SFTP1, SFTPA1B, SP-A, SP-A1, SP-A1 beta, SP-A1 delta, SP-A1 epsilon, SP-A1 gamma, SPA, SPA1 |
|
|
786
|
|
|
Solute carrier family 6 member 9 |
GCENSG, GLYT1 |
Arthrogryposis multiplex congenita, Attention deficit hyperactivity disorder, Congenital clubfoot, Congenital genu recurvatum, Developmental delay, Dolichocephaly, Dysphagia, Elbow flexion contracture, Epileptic encephalopathy, Glycine encephalopathy, Glycine encephalopathy with normal serum glycine, Hip contracture, Hypoplasia of corpus callosum, Nonorganic psychosis, Optic atrophy, Psychosis, Ptosis, Respiratory failure, Schizophrenia, TrigonocephalyView all (5 more) |
|
787
|
|
|
Solute carrier family 6 member 11 |
GAT-3, GAT3, GAT4 |
|
|
788
|
|
|
Solute carrier family 6 member 12 |
BGT-1, BGT1, GAT2 |
|
|
789
|
|
|
Solute carrier family 6 member 13 |
GAT-2, GAT2, GAT3 |
|
|
790
|
|
|
Solute carrier family 7 member 1 |
ATRC1, CAT-1, ERR, HCAT1, REC1L |
|
