|
641
|
|
|
S100 calcium binding protein B |
NEF, S100, S100-B, S100beta |
Bipolar disorder, Brain neoplasms, Intracranial neoplasm, Cerebral vasospasm, Disruptive behavior disorder, Down syndrome, Intracranial vasospasm, Manic disorder, Mental depression, Mood disorder, Myocardial infarction, Oppositional defiant disorder, Schizophrenia, Trisomy 21 |
|
642
|
|
|
S100 calcium binding protein P |
MIG9 |
|
|
643
|
|
|
Serum amyloid A1 |
PIG4, SAA, SAA2, TP53I4 |
Aa amyloidosis, Amyloid nephropathy, Cholestasis, Congenital heart defects, Dermatitis, Hypothyroidism, Kidney disease, Malabsorption syndrome, Malnutrition, Nephrotic syndrome, Reactive systemic amyloidosis |
|
644
|
|
|
Serum amyloid A2 |
SAA, SAA1 |
|
|
645
|
|
|
S-antigen visual arrestin |
RP47, RP96, S-AG |
Cataract, Chorioretinal atrophy, Congenital hypoplasia of penis, Congenital stationary night blindness, Diabetes mellitus, Disorder of eye, Glaucoma, Hearing loss, Hemeralopia, Hyperinsulinism, Hypogonadism, Hypoplasia of optic disc, Keratoconus, Mental retardation, Myopia, Night blindness, Nyctalopia, Nystagmus, Obesity, Oguchi disease, Optic atrophy, Retinitis pigmentosa, Rod-cone dystrophy, Strabismus, Uveitis, Congenital stationary night blindness, x-linkedView all (11 more) |
|
646
|
|
|
Spalt like transcription factor 2 |
COLB, HSAL2, Sal-2, ZNF795, p150(Sal2) |
|
|
647
|
|
|
Spalt like transcription factor 1 |
HEL-S-89, HSAL1, Sal-1, TBS, ZNF794 |
Agenesis of corpus callosum, Arnold-chiari malformation, Atrial septal defect, Blepharophimosis, Bowel incontinence, Camptodactyly of fingers, Cataract, Clinodactyly, Congenital anomaly of limb, Congenital coloboma of iris, Congenital exomphalos, Congenital hypoplasia of penis, Congenital malformation of the urinary system, Cranial nerve paralysis, Cryptorchidism, Duodenal atresia, Dwarfism, Ectopic kidney, Fundus coloboma, Gastroesophageal reflux disease, Hearing loss, Hypospadias, Hypothyroidism, Imperforate anus, Macrostomia, Macrotia, Mental retardation, Microcephaly, Microphthalmos, Microtia, Multicystic renal dysplasia, Multiple renal cysts, Patent ductus arteriosus, Polydactyly, Renal dysplasia, Renal glomerular disease, Renal hypoplasia, Renal insufficiency, Retinal coloboma, Strabismus, Syndactyly of the toes, Tetralogy of fallot, Townes syndrome, Townes-brocks syndrome, Townes-brocks-branchiootorenal-like syndrome, Uterine anomalies, Vesicoureteral refluxView all (32 more) |
|
648
|
|
|
Seryl-tRNA synthetase 1 |
NEDMAS, SARS, SERRS, SERS |
Absence of septum pellucidum, Autism, Central visual impairment, Cerebral atrophy, Coronary artery disease, Cortical dysplasia, Developmental delay, Dyskinetic syndrome, Dyssomnia, Hypoplasia of corpus callosum, Mental retardation, Mental depression, Microcephaly, Motor delay, Neurodevelopmental disorder with microcephaly, ataxia, and seizures, Polymicrogyria, Salaam seizures, Seizure, Sleep disorders, Stereotyped behaviorView all (5 more) |
|
649
|
|
|
Solute carrier family 22 member 23 |
C6orf85 |
|
|
650
|
|
|
Spermidine/spermine N1-acetyltransferase 1 |
DC21, KFSD, KFSDX, SAT, SSAT, SSAT-1 |
|
