|
721
|
|
|
Sarcoglycan beta |
A3b, LGMD2E, LGMDR4, SGC |
|
|
722
|
|
|
Sarcoglycan delta |
35DAG, CMD1L, DAGD, LGMDR6, SG-delta, SGCDP, SGD |
Amyotrophy, Limb-girdle muscular dystrophy, Cardiomyopathy, Chronic obstructive pulmonary disease, Colorectal neoplasms, Congestive heart failure, Diabetes mellitus, Dilated cardiomyopathy, Facial paralysis, Hearing loss, Kawasaki disease, Limb muscle atrophy, Lipoatrophy, Lipodystrophy, Muscular dystrophy, Myocardial diseases, Myopathy, Neuromuscular diseases, Palmoplantar keratoderma, Schizophrenia, Ventricular hypertrophyView all (6 more) |
|
723
|
|
|
Sarcoglycan gamma |
35DAG, A4, DAGA4, DMDA, DMDA1, LGMD2C, LGMDR5, MAM, SCARMD2, gamma-SG |
Arthritis, Diabetes mellitus, Leukemia, Limb-girdle muscular dystrophy, Macroglossia, Muscular dystrophy, Osteoarthrosis deformans, Scoliosis, Ventricular hypertrophy, Ventricular systolic dysfunction, Right ventricular dilatation |
|
724
|
|
|
Serum/glucocorticoid regulated kinase 1 |
SGK |
Alzheimer disease, Anaplastic carcinoma, Asymmetric diabetic proximal motor neuropathy, Carcinoma, Diabetic amyotrophy, Diabetic asymmetric polyneuropathy, Diabetic autonomic neuropathy, Diabetic mononeuropathy, Diabetic nephropathy, Diabetic neuralgia, Diabetic polyneuropathy, Diffuse lymphoma, Kidney disease, Leukemia, Mental depression, Myeloid leukemia, Symmetric diabetic proximal motor neuropathy, UremiaView all (3 more) |
|
725
|
|
|
Secretogranin V |
7B2, P7B2, SGNE1, SgV |
|
|
726
|
|
|
N-sulfoglucosamine sulfohydrolase |
HSS, MPS3A, SFMD |
Autism, Bowel incontinence, Developmental delay, Developmental regression, Dysmorphic features, Dyssomnia, Hypoplasia of corpus callosum, Mental retardation, Movement disorders, Mucopolysaccharidosis, Nystagmus, Pfaundler-hurler syndrome, Retinal dystrophy, Sanfilippo syndrome, Septal hypertrophy, Sleep disorders, SynophrysView all (2 more) |
|
727
|
|
|
SH3 domain binding protein 2 |
3BP-2, 3BP2, CRBM, CRPM, RES4-23 |
Atrophy, Autoinflammatory disease, Cervical lymphadenopathy, Cherubism, Huntington disease, Hypodontia, Multiple sclerosis, Oligodontia, Optic atrophy, Proptosis, Sleep apnea |
|
728
|
|
|
Sphingomyelin phosphodiesterase 4 pseudogene 1 |
- |
|
|
729
|
|
|
SH3 domain containing GRB2 like 1, endophilin A2 |
CNSA1, EEN, SH3D2B, SH3P8 |
|
|
730
|
|
|
SH3 domain containing GRB2 like 2, endophilin A1 |
CNSA2, EEN-B1, SH3D2A, SH3P4 |
|
