|
811
|
|
|
Solute carrier family 18 member A3 |
CMS21, VACHT |
Acquired kyphoscoliosis, Arthrogryposis multiplex congenita, Bulbar palsy, Developmental dysplasia of the hip, Congenital kyphoscoliosis, Myasthenic syndrome, Congenital pectus carinatum, Distal amyotrophy, Dysphagia, Esotropia, Facial paralysis, Fetal akinesia deformation sequence, Gastroesophageal reflux disease, Hearing loss, High palate, Mental retardation, Motor delay, Myasthenia gravis, Nystagmus, Pena shokeir syndrome, Polyneuropathy, Ptosis, Sleep apnea, Sudden episodic apneaView all (9 more) |
|
812
|
|
|
Solute carrier family 19 member 1 |
CHMD, FOLT, IFC-1, IFC1, IMD114, MEGAF, REFC, RFC, RFC1, RFT-1, hRFC, hSLC19A1 |
Adenoma, Autism, Urinary bladder cancer, Bladder neoplasm, Breast cancer, Cataract, Colonic neoplasms, Colorectal cancer, Colorectal neoplasms, Down syndrome, Knobloch syndrome, Lymphoblastic leukemia, Lung adenocarcinoma, Macular dystrophy, Myopia, Nervous system disorder, Nystagmus, Oestrogen receptor positive breast cancer, Pancreatic cancer, Papillary adenoma, Pelvic organ prolapse, Retinal dystrophy, Retinitis pigmentosa, Trisomy 21View all (9 more) |
|
813
|
|
|
Solute carrier family 20 member 1 |
GLVR1, Glvr-1, PIT1, PiT-1 |
|
|
814
|
|
|
Solute carrier family 20 member 2 |
GLVR-2, GLVR2, IBGC1, IBGC2, IBGC3, MLVAR, PIT-2, PIT2, RAM1, Ram-1 |
Anxiety disorder, Basal ganglia calcification, Basal ganglia diseases, Bilateral striopallidodentate calcinosis, Brain calcification, Congenital anomaly of ischium, Dysarthria, Extrapyramidal disease, Fahr`s syndrome, Lenticulostriate disorders, Leukemia, Malformation of cortical development, Mental depression, Microcephaly, Obsessive-compulsive disorder, Osteopenia, Parkinson disease, Psychosis, Subcutaneous hemorrhage, Tumoral calcinosis, UrticariaView all (6 more) |
|
815
|
|
|
Solute carrier family 25 member 1 |
CIC, CMS23, CTP, D2L2AD, SEA, SLC20A3 |
Acquired kyphoscoliosis, Agenesis of corpus callosum, Arthrogryposis multiplex congenita, Bulbar palsy, Cerebellar hypoplasia, Developmental dysplasia of the hip, Congenital kyphoscoliosis, Myasthenic syndrome, Congenital pectus carinatum, Developmental delay, Distal amyotrophy, Dysphagia, Epileptic encephalopathy, Esotropia, Gastroesophageal reflux disease, Hearing loss, High palate, Hydrocephalus, Mental retardation, Micrognathism, Motor delay, Myasthenia gravis, Nystagmus, Polyneuropathy, Ptosis, Sleep apnea, Spina bifida, Sudden episodic apnea, Ventricular septal defectView all (14 more) |
|
816
|
|
|
Solute carrier organic anion transporter family member 2A1 |
MATR1, OATP2A1, PGT, PHOAD, PHOAR2, SLC21A2 |
Acne, Anemia, Arthritis, Cerebral palsy, Colonic neoplasms, Colorectal adenoma, Colorectal cancer, Colorectal neoplasms, Cranioosteoarthropathy, Cutis verticis gyrata, Eczema, Enteropathy associated with slco2a1 gene, Gynecomastia, Hereditary clubbing, Hyperostosis, Hypertrophic osteoarthropathy, Lung neoplasms, Malabsorption syndrome, Osteomyelitis, Osteoporosis, Pachydermoperiostosis syndrome, Palmoplantar keratoderma, Peptic ulcer, Periostosis, Prostate cancer, Ptosis, Scoliosis, Seborrheic dermatitis, Skin neoplasmsView all (14 more) |
|
817
|
|
|
Solute carrier organic anion transporter family member 1A2 |
OATP, OATP-A, OATP1A2, SLC21A3 |
|
|
818
|
|
|
Solute carrier family 22 member 1 |
HOCT1, OCT1, oct1_cds |
|
|
819
|
|
|
Solute carrier family 22 member 3 |
EMT, EMTH, OCT3 |
Autism, Carditis, Colonic neoplasms, Colorectal cancer, Colorectal neoplasms, Coronary artery disease, Coronary heart disease, Diabetes mellitus, Myocarditis, Nasopharyngeal carcinoma, Obesity, Prostatic neoplasms, Prostate cancer |
|
820
|
|
|
Solute carrier family 22 member 2 |
Oct-02 |
|
