|
1131
|
|
|
Solute carrier family 39 member 13 |
EDSSPD3, LZT-Hs9, SCDEDS, ZIP13 |
Bone disease, Connective tissue disease, Dwarfism, Ehlers-danlos syndrome, High palate, Hypodontia, Odontome, Osteochondrodysplasia, Osteopenia, Proptosis, Skeletal dysplasia, Spondylocheirodysplasia, ehlers-danlos syndrome-like, Spondylodysplastic ehlers-danlos syndrome, Spondyloenchondrodysplasia with abnormal dentition |
|
1132
|
|
|
Structural maintenance of chromosomes 3 |
BAM, BMH, CDLS3, CSPG6, HCAP, SMC3L1 |
Anxiety disorder, Atrial septal defect, Attention deficit hyperactivity disorder, Autism, Brachycephaly, Brachydactyly, Camptodactyly of fingers, Cataract, Cerebral cortical atrophy, Choanal atresia, Congenital diaphragmatic hernia, Congenital hypoplasia of penis, Congenital malrotation of intestine, Congenital muscular hypertrophy-cerebral syndrome, Congenital pectus excavatum, Cornelia de lange syndrome, Cryptorchidism, Cutis marmorata, Developmental delay, Dwarfism, Dyssomnia, Gastroesophageal reflux disease, Glaucoma, Growth deficiency and mental retardation with facial dysmorphism, Hearing loss, High palate, Hypoplasia of nipple, Hypospadias, Impaired cognition, Mental retardation, Intestinal volvulus, Macrotia, Microcephaly, Microcornea, Micrognathism, Micromelia, Monocytic leukemia, Multicystic renal dysplasia, Myeloid leukemia, Myopia, Nervous system diseases, Neurodevelopmental disorders, Nystagmus, Obsessive-compulsive disorder, Oligodactyly, Phthisis bulbi, Physiologic amenorrhea, Ptosis, Pulmonary stenosis, Radioulnar synostosis, Renal insufficiency, Sleep disorders, Speech disorders, Strabismus, Syndactyly of the toes, Synophrys, Talipes, Uterine anomalies, Ventricular septal defect, Vesicoureteral refluxView all (45 more) |
|
1133
|
|
|
SEC14 and spectrin domain containing 1 |
Solo |
|
|
1134
|
|
|
Synaptogyrin 2 |
- |
|
|
1135
|
|
|
Synaptogyrin 1 |
- |
|
|
1136
|
|
|
Solute carrier family 6 member 5 |
GLYT-2, GLYT2, HKPX3, NET1 |
Breast cancer, Congenital exomphalos, Dyssomnia, Epileptic encephalopathy, Eosinophilia, Gastroesophageal reflux disease, Hereditary hyperekplexia, Hiatal hernia, Hyperekplexia, Mental retardation, Schizophrenia, Sleep disorders |
|
1137
|
|
|
Solute carrier family 28 member 1 |
CNT1, HCNT1, URCTU |
|
|
1138
|
|
|
Single-pass membrane protein with aspartate rich tail 1 |
C22orf32, DDDD, EMRE |
|
|
1139
|
|
|
SR-related CTD associated factor 11 |
CASP11, SFRS2IP, SIP1, SRRP129, SRSF2IP |
|
|
1140
|
|
|
Solute carrier family 24 member 1 |
CSNB1D, HsT17412, NCKX, NCKX1, RODX |
Congenital stationary night blindness, Disorder of eye, Hypoplasia of optic disc, Myopia, Night blindness, Nyctalopia, Nystagmus, Retinitis pigmentosa, Strabismus, Congenital stationary night blindness, x-linked |
