|
481
|
|
|
Sclerostin |
CDD, DAND6, SOST1, VBCH |
Mallet finger, Chondrodystrophic myotonia, Congenital anomaly of nose, Cranial nerve paralysis, Craniodiaphyseal dysplasia, Diaphyseal dysplasia, Dwarfism, Dyschondroplasias, Esotropia, Facial paralysis, Fingernail dysplasia, Frontal bossing, Hearing loss, Hyperostosis of skull, Impaired cognition, Macrocephaly, Malocclusion, Melnick-needles syndrome, Mental retardation, Multiple epiphyseal dysplasia, Nail diseases, Nail dysplasia, Nystagmus, Optic atrophy, Osteochondrodysplasia, Osteosclerosis, Papilledema, Proptosis, Ptosis, Schwartz-jampel syndrome, Sclerosteosis, Spondyloenchondrodysplasia, Spondyloepiphyseal dysplasia, Stenosis of external auditory canal, Syndactyly of fingers, Van buchem diseaseView all (21 more) |
|
482
|
|
|
Serpin family A member 5 |
PAI-3, PAI3, PCI, PCI-B, PLANH3, PROCI |
|
|
483
|
|
|
ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 3 |
SIAT8C, ST8SiaIII |
|
|
484
|
|
|
Ssu-2 homolog |
C3orf32, SSU-2, fls485 |
|
|
485
|
|
|
Sep (O-phosphoserine) tRNA:Sec (selenocysteine) tRNA synthase |
LP, PCH2D, SLA, SLA-p35, SLA/LP, SecS |
Arthrogryposis multiplex congenita, Cerebellar atrophy, Cerebellar hypoplasia, Cerebral atrophy, Developmental delay, Dysarthria, Dyskinetic syndrome, Dyssomnia, Exotropia, Hypoglycemia, Hypoplasia of corpus callosum, Spastic diplegia, Nystagmus, Pontoneocerebellar hypoplasia, Progressive cerebello-cerebral atrophy, Ptosis, Sleep disorders, Spastic quadriplegiaView all (3 more) |
|
486
|
|
|
SID1 transmembrane family member 2 |
CGI-40 |
|
|
487
|
|
|
SBDS ribosome maturation factor |
CGI-97, SDO1, SDS, SWDS |
Anemia, Aphthous ulcer, Aplastic anemia, Congenital alveolar dysplasia, Congenital pectus carinatum, Developmental delay, Diabetes mellitus, Dwarfism, Eczema, Exocrine pancreatic insufficiency, Hypoplastic anemia, Ichthyosis, Leukemia, Malabsorption syndrome, Mental retardation, Metaphyseal chondrodysplasia, Microdontia, Miller dieker syndrome, Monocytic leukemia, Myelodysplasia, Myelodysplastic syndrome, Myocardial infarction, Myocardial necrosis, Nephrocalcinosis, Neutropenia, Osteopenia, Pancytopenia, Scoliosis, Shwachman syndrome, Shwachman-diamond syndrome, Slipped capital femoral epiphyses, Specific learning disorderView all (17 more) |
|
488
|
|
|
Secretion associated Ras related GTPase 1B |
ANDD, CMRD, GTBPB, SARA2 |
|
|
489
|
|
|
Stromal cell derived factor 4 |
Cab45, SDF-4 |
|
|
490
|
|
|
Solute carrier family 45 member 2 |
1A1, AIM1, MATP, OCA4, SHEP5 |
|
