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#617936 - BUTYRYLCHOLINESTERASE DEFICIENCY; BCHED
SUXAMETHONIUM SENSITIVITY, INCLUDED
Cytogenetic locations: 12881446
Gene summaries Genetic tests Medical literature
#204870 - CORNEAL DYSTROPHY, GELATINOUS DROP-LIKE; GDLD
Cytogenetic locations: 19758629
#156500 - METAPHYSEAL CHONDRODYSPLASIA, SCHMID TYPE; MCDS
Cytogenetic locations: 18220429
#615896 - HYPOTRICHOSIS 13; HYPT13
Cytogenetic locations: 22592156
#615749 - ECULIZUMAB, POOR RESPONSE TO
Cytogenetic locations: CHDT3
#614229 - SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 11; SCAR11
Cytogenetic locations: 21835308
#614723 - ADENINE PHOSPHORIBOSYLTRANSFERASE DEFICIENCY; APRTD
Cytogenetic locations: 11349690
#616115 - FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 4; FCAS4
Cytogenetic locations: [Fasting
#616948 - SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 22; SCAR22
Cytogenetic locations: ?SERPINE2
#614212 - ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 4; IIAE4
Cytogenetic locations: 20934285
#615193 - BLEEDING DISORDER, PLATELET-TYPE, 15; BDPLT15
Cytogenetic locations: 23434115
#301015 - HEMOLYTIC ANEMIA, CONGENITAL, X-LINKED; HACXL
Cytogenetic locations: 26944472
#615517 - HEMOCHROMATOSIS, TYPE 5; HFE5
Cytogenetic locations: 11389486
#618075 - EPILEPSY, FAMILIAL ADULT MYOCLONIC, 7; FAME7
Cytogenetic locations: 29507423
#616435 - FANCONI ANEMIA, COMPLEMENTATION GROUP T; FANCT
Cytogenetic locations: 26046368
#618637 - OCULOPHARYNGEAL MYOPATHY WITH LEUKOENCEPHALOPATHY 1; OPML1
Cytogenetic locations: 31332380
#619340 - DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 96; DEE96
Cytogenetic locations: {Autism
#601068 - EPILEPSY, FAMILIAL ADULT MYOCLONIC, 1; FAME1
Cytogenetic locations: 15747356
#614302 - EMERY-DREIFUSS MUSCULAR DYSTROPHY 7, AUTOSOMAL DOMINANT; EDMD7
Cytogenetic locations: 21391237
#305390 - EXUDATIVE VITREORETINOPATHY 2, X-LINKED; EVR2
Cytogenetic locations: 29299244
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