|
1171
|
|
|
Sperm associated antigen 6 |
CFAP194, CT141, FAP194, Repro-SA-1, pf16 |
|
|
1172
|
|
|
SRY-box transcription factor 13 |
ICA12, Sox-13 |
|
|
1173
|
|
|
Synuclein alpha interacting protein |
SYPH1, Sph1 |
|
|
1174
|
|
|
SEC24 homolog C, COPII component |
- |
22q11 deletion syndrome, 22q11 partial monosomy syndrome, 22q11.2 deletion syndrome, Acne, Acrocephaly, Anxiety disorder, Arachnodactyly, Arrhinencephaly, Arthritis, Asthma, Asymmetric crying face association, Atrial septal defect, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Bowel incontinence, Cataract, Choanal atresia, Cholelithiasis, Chronic obstructive pulmonary disease, Congenital clubfoot, Congenital epicanthus, Congenital exomphalos, Congenital hypoplasia of thymus, Congenital malrotation of intestine, Conotruncal anomaly face syndrome, Corneal neovascularization, Cryptorchidism, Developmental delay, Digeorge syndrome, Dwarfism, Dysphasia, Gastroesophageal reflux disease, Glaucoma, Hearing loss, Hirschsprung disease, Hydrocephalus, Hyperthyroidism, Hypoparathyroidism, Hypospadias, Hypothyroidism, Immunologic deficiency syndromes, Imperforate anus, Laryngomalacia, Major affective disorder, Mental depression, Mental retardation, Microcephaly, Micrognathism, Microphthalmos, Microstomia, Multiple renal cysts, Myelomeningocele, Obesity, Optic atrophy, Otitis media, Patent ductus arteriosus, Persistent truncus arteriosus, Platybasia, Polycystic kidney disease, Polydactyly of toes, Posterior embryotoxon, Ptosis, Renal hypoplasia, Schizophrenia, Scoliosis, Seborrheic dermatitis, Shprintzen syndrome, Specific learning disorder, Strabismus, Tetralogy of fallot, Tricuspid atresia, Uterine anomalies, Ventricular septal defect, Vesicoureteral reflux, Vulval varicesView all (61 more) |
|
1175
|
|
|
SH3 and PX domains 2A |
FISH, SH3MD1, TKS5 |
|
|
1176
|
|
|
Syndecan 3 |
SDCN, SYND3 |
|
|
1177
|
|
|
Solute carrier family 25 member 44 |
- |
|
|
1178
|
|
|
ST18 C2H2C-type zinc finger transcription factor |
NZF-3, NZF3, ZC2H2C3, ZC2HC10, ZNF387 |
|
|
1179
|
|
|
SEC14 like lipid binding 5 |
PRELID4B |
|
|
1180
|
|
|
Semaphorin 3E |
M-SEMAH, M-SemaK, SEMAH, coll-5 |
Aneurysm of aortic arch, Aqueductal stenosis, Atrial septal defect, Attention deficit hyperactivity disorder, Autism, Brachydactyly, Camptodactyly of fingers, Charge syndrome, Choanal atresia, Congenital coloboma of iris, Congenital epicanthus, Congenital exomphalos, Congenital omphalocele, Cryptorchidism, Dandy-walker syndrome, Developmental delay, Double outlet right ventricle, Duodenal atresia, Dwarfism, Dysphagia, Esophageal atresia, Facial paralysis, Fundus coloboma, Gastroesophageal reflux disease, Gonadotropin deficiency, Gynecomastia, Hearing loss, Heart septal defects, Holoprosencephaly, Horseshoe kidney, Hydronephrosis, Hypogonadism, Hypogonadotropic hypogonadism, Hypopituitarism, Hypoplasia of thumb, Hypothyroidism, Imperforate anus, Interrupted aortic arch, Isolated somatotropin deficiency, Laryngomalacia, Lymphopenia, Mental retardation, Microcephaly, Micrognathism, Microphthalmos, Microstomia, Microtia, Neck webbing, Nystagmus, Obsessive-compulsive disorder, Optic atrophy, Parathyroid hypoplasia, Patent ductus arteriosus, Penis agenesis, Physiologic amenorrhea, Ptosis, Pulmonary stenosis, Renal agenesis, Renal hypoplasia, Retinal coloboma, Scoliosis, Somatotropin deficiency, Strabismus, Syndromic microphthalmia, Talipes, Tetralogy of fallot, Ventricular septal defect, Vesicoureteral refluxView all (53 more) |
