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Search Results for - VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 6

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ID
 
Description
 
Product
 
Source
(Showing Items: 50)
 
 
 
 
VITILIGO | HASHIMOTO THYROIDITIS
 
LCL
 
B-Lymphocyte
 
 
 
 
VITILIGO | HASHIMOTO THYROIDITIS
 
LCL
 
B-Lymphocyte
 
 
 
 
SPECIFIC ANTIBODY DEFICIENCY WITH NORMAL IMMUNOGLOBULINS | ULCERATIVE COLITIS, SUSCEPTIBILITY TO
 
LCL
 
B-Lymphocyte
 
 
 
 
MULTIPLE SCLEROSIS; MS
 
DNA
 
LCL
 
 
 
 
MULTIPLE SCLEROSIS; MS
 
LCL
 
B-Lymphocyte
 
 
 
 
NIJMEGEN BREAKAGE SYNDROME | NIJMEGEN BREAKAGE SYNDROME GENE; NBS1
 
DNA
 
LCL
 
 
 
 
EPILEPSY, CHILDHOOD ABSENCE, 1; ECA1 | MONOZYGOTIC TWIN PAIRS
 
LCL
 
B-Lymphocyte
 
 
 
 
PERSONAL GENOME PROJECT
 
LCL
 
B-Lymphocyte
 
 
 
 
NIJMEGEN BREAKAGE SYNDROME | NIJMEGEN BREAKAGE SYNDROME GENE; NBS1
 
DNA
 
LCL
 
 
 
 
NIJMEGEN BREAKAGE SYNDROME | NIJMEGEN BREAKAGE SYNDROME GENE; NBS1
 
LCL
 
B-Lymphocyte
 
 
 
 
NIJMEGEN BREAKAGE SYNDROME | NIJMEGEN BREAKAGE SYNDROME GENE; NBS1
 
LCL
 
B-Lymphocyte
 
 
 
 
MULTIPLE SCLEROSIS; MS
 
LCL
 
B-Lymphocyte
 
 
 
 
MULTIPLE SCLEROSIS; MS
 
DNA
 
LCL
 
 
 
 
MULTIPLE SCLEROSIS; MS
 
LCL
 
B-Lymphocyte
 
 
 
 
MULTIPLE SCLEROSIS; MS
 
DNA
 
LCL
 
 
 
 
MULTIPLE SCLEROSIS; MS
 
DNA
 
LCL
 
 
 
 
MULTIPLE SCLEROSIS; MS
 
DNA
 
LCL
 
 
 
 
MULTIPLE SCLEROSIS; MS
 
DNA
 
LCL
 
 
 
 
MULTIPLE SCLEROSIS; MS
 
DNA
 
LCL
 
 
 
 
MULTIPLE SCLEROSIS; MS
 
LCL
 
B-Lymphocyte
 
 
 
 
MULTIPLE SCLEROSIS; MS
 
LCL
 
B-Lymphocyte
 
 
 
 
MULTIPLE SCLEROSIS; MS
 
LCL
 
B-Lymphocyte
 
 
 
 
MULTIPLE SCLEROSIS; MS
 
LCL
 
B-Lymphocyte
 
 
 
 
MULTIPLE SCLEROSIS; MS
 
LCL
 
B-Lymphocyte
 
 
 
 
MULTIPLE SCLEROSIS; MS
 
LCL
 
B-Lymphocyte
 
 
 
 
MULTIPLE SCLEROSIS; MS
 
LCL
 
B-Lymphocyte
 
 
 
 
MULTIPLE SCLEROSIS; MS
 
LCL
 
B-Lymphocyte
 
 
 
 
MULTIPLE SCLEROSIS; MS
 
LCL
 
B-Lymphocyte
 
 
 
 
MULTIPLE SCLEROSIS; MS
 
LCL
 
B-Lymphocyte
 
 
 
 
MULTIPLE SCLEROSIS; MS
 
DNA
 
LCL
 
 
 
 
MULTIPLE SCLEROSIS; MS
 
LCL
 
B-Lymphocyte
 
 
 
 
MULTIPLE SCLEROSIS; MS
 
DNA
 
LCL
 
 
 
 
MULTIPLE SCLEROSIS; MS
 
LCL
 
B-Lymphocyte
 
 
 
 
MULTIPLE SCLEROSIS; MS
 
DNA
 
LCL
 
 
 
 
MULTIPLE SCLEROSIS; MS
 
DNA
 
LCL
 
 
 
 
LYMPHOPROLIFERATIVE SYNDROME, X-LINKED | SH2 DOMAIN PROTEIN 1A; SH2D1A
 
LCL
 
B-Lymphocyte
 
 
 
 
ATAXIA-TELANGIECTASIA; AT
 
LCL
 
B-Lymphocyte
 
 
 
 
ATAXIA-TELANGIECTASIA; AT | ATAXIA-TELANGIECTASIA MUTATED GENE; ATM
 
LCL
 
B-Lymphocyte
 
 
 
 
LYMPHOPROLIFERATIVE SYNDROME, X-LINKED | SH2 DOMAIN PROTEIN 1A; SH2D1A
 
DNA
 
LCL
 
 
 
 
LYMPHOPROLIFERATIVE SYNDROME, X-LINKED | SH2 DOMAIN PROTEIN 1A; SH2D1A
 
LCL
 
B-Lymphocyte
 
 
 
 
CENTRAL CORE DISEASE OF MUSCLE | MALIGNANT HYPERTHERMIA SUSCEPTIBILITY 1; MHS1 | RYANODINE RECEPTOR 1; RYR1
 
LCL
 
B-Lymphocyte
 
 
 
 
CONGENITAL DISORDER OF DEGLYCOSYLATION; CDDG | N-GLYCANASE 1; NGLY1 | MALIGNANT HYPERTHERMIA SUSCEPTIBILITY 5; MHS5 | CALCIUM CHANNEL, VOLTAGE-DEPENDENT, L TYPE, ALPHA-1S SUBUNIT; CACNA1S
 
iPSC
 
Fibroblast
 
 
 
 
CONGENITAL DISORDER OF DEGLYCOSYLATION; CDDG | N-GLYCANASE 1; NGLY1 | MALIGNANT HYPERTHERMIA SUSCEPTIBILITY 5; MHS5 | CALCIUM CHANNEL, VOLTAGE-DEPENDENT, L TYPE, ALPHA-1S SUBUNIT; CACNA1S
 
LCL
 
B-Lymphocyte
 
 
 
 
CONGENITAL DISORDER OF DEGLYCOSYLATION; CDDG | N-GLYCANASE 1; NGLY1 | MALIGNANT HYPERTHERMIA SUSCEPTIBILITY 5; MHS5 | CALCIUM CHANNEL, VOLTAGE-DEPENDENT, L TYPE, ALPHA-1S SUBUNIT; CACNA1S
 
Fibroblast
 
Skin, Skin
 
 
 
 
CONGENITAL DISORDER OF DEGLYCOSYLATION; CDDG | N-GLYCANASE 1; NGLY1 | MALIGNANT HYPERTHERMIA SUSCEPTIBILITY 5; MHS5 | CALCIUM CHANNEL, VOLTAGE-DEPENDENT, L TYPE, ALPHA-1S SUBUNIT; CACNA1S
 
Fibroblast
 
Skin, Skin
 
 
 
 
CONGENITAL DISORDER OF DEGLYCOSYLATION; CDDG | N-GLYCANASE 1; NGLY1 | MALIGNANT HYPERTHERMIA SUSCEPTIBILITY 5; MHS5 | CALCIUM CHANNEL, VOLTAGE-DEPENDENT, L TYPE, ALPHA-1S SUBUNIT; CACNA1S
 
LCL
 
B-Lymphocyte
 
 
 
 
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE III; HSAN3 | HIRSCHSPRUNG DISEASE | INHIBITOR OF KAPPA LIGHT POLYPEPTIDE GENE ENHANCER IN B CELLS, KINASE-COMPLEX ASSOCIATED PROTEIN; IKBKAP
 
DNA
 
LCL
 
 
 
 
CEREBRAL CREATINE DEFICIENCY SYNDROME 1; CCDS1 | SOLUTE CARRIER FAMILY 6 (NEUROTRANSMITTER TRANSPORTER, CREATINE), MEMBER 8; SLC6A8
 
LCL
 
B-Lymphocyte
 
 
 
 
MYELOMA, MULTIPLE AMYLOIDOSIS, PRIMARY, INCLUDED; AL, INCLUDED
 
LCL
 
B-Lymphocyte
 
 
 
 
PARKINSON DISEASE | ESSENTIAL TREMOR-MOVEMENT DISORDER | RESTLESS LEG SYNDROME | PD
 
LCL
 
B-Lymphocyte

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