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#619924 - IMMUNODEFICIENCY 105, SEVERE COMBINED; IMD105
Cytogenetic locations: 134370
Gene summaries Genetic tests Medical literature
*601554 - DYNEIN, LIGHT CHAIN, TCTEX TYPE, 1; DYNLT1
Cytogenetic locations: 28646886
*601364 - CADHERIN 13; CDH13
Cytogenetic locations: 617332
*604895 - T-BOX TRANSCRIPTION FACTOR 21; TBX21
Cytogenetic locations: 600242
*604615 - EOMESODERMIN; EOMES
Cytogenetic locations: 19888994
*607904 - CALCIUM CHANNEL, VOLTAGE-DEPENDENT, T TYPE, ALPHA-1H SUBUNIT; CACNA1H
Cytogenetic locations: 12853961
*604065 - CALCIUM CHANNEL, VOLTAGE-DEPENDENT, T TYPE, ALPHA-1G SUBUNIT; CACNA1G
Cytogenetic locations: 29495342
#612132 - ECTODERMAL DYSPLASIA AND IMMUNODEFICIENCY 2; EDAID2
Cytogenetic locations: 23864385
*166490 - SECRETED PHOSPHOPROTEIN 1; SPP1
Cytogenetic locations: 604852
*603149 - INTERLEUKIN 17A; IL17A
Cytogenetic locations: Houge-Janssens
#130080 - EHLERS-DANLOS SYNDROME, PERIODONTAL TYPE, 1; EDSPD1
Cytogenetic locations: 12875936
#302800 - CHARCOT-MARIE-TOOTH DISEASE, X-LINKED DOMINANT, 1; CMTX1
Cytogenetic locations: 21282593
*300292 - FORKHEAD BOX P3; FOXP3
Cytogenetic locations: 300202
*606885 - ACYL-CoA DEHYDROGENASE, SHORT-CHAIN; ACADS
Cytogenetic locations: 18054510
*147570 - INTERFERON, GAMMA; IFNG
Cytogenetic locations: 17352260
*605723 - PROGRAMMED CELL DEATH 1 LIGAND 2; PDCD1LG2
Cytogenetic locations: 16864790
*151460 - PROTEIN-TYROSINE PHOSPHATASE, RECEPTOR-TYPE, C; PTPRC
Cytogenetic locations: 12134145
%612417 - NARCOLEPSY 4, SUSCEPTIBILITY TO; NRCLP4
Cytogenetic locations: 18820697
*151385 - RUNT-RELATED TRANSCRIPTION FACTOR 1; RUNX1
AML1/TEL FUSION GENE, INCLUDED
Cytogenetic locations: 11388043
*603517 - B-CELL CLL/LYMPHOMA 10; BCL10
Cytogenetic locations: 12910267
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