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%613318 - MIYOSHI MUSCULAR DYSTROPHY 2; MMD2
Gene summaries Genetic tests Medical literature
*607909 - ANTIZYME INHIBITOR 1; AZIN1
*606602 - BRAIN AND ACUTE LEUKEMIA GENE, CYTOPLASMIC; BAALC
*603097 - ATPase, H+ TRANSPORTING, LYSOSOMAL, 42-KD, V1 SUBUNIT C, ISOFORM 1; ATP6V1C1
Cytogenetic locations: 601147
*182878 - OUTER DENSE FIBER OF SPERM TAILS 1; ODF1
Cytogenetic locations: ##Z##
#616839 - EXERCISE INTOLERANCE, RIBOFLAVIN-RESPONSIVE; RREI
Cytogenetic locations: ######
*619526 - ZINC FINGER PROTEIN 706; ZNF706
Cytogenetic locations: ##s###
*619839 - SORTING NEXIN 31; SNX31
#616029 - ECTODERMAL DYSPLASIA/SHORT STATURE SYNDROME; ECTDS
Cytogenetic locations: 612959
#608641 - DEAFNESS, AUTOSOMAL DOMINANT 28; DFNA28
Cytogenetic locations: Esrp1
*601878 - KRUPPEL-LIKE FACTOR 10; KLF10
*616196 - DDB1- AND CUL4-ASSOCIATED FACTOR 13; DCAF13
#618970 - CONE-ROD SYNAPTIC DISORDER SYNDROME, CONGENITAL NONPROGRESSIVE; CRSDS
Cytogenetic locations: ###?##
*605933 - DENDROCYTE-EXPRESSED 7-TRANSMEMBRANE PROTEIN; DCSTAMP
Cytogenetic locations: 614721
*608413 - UBIQUITIN-PROTEIN LIGASE E3 COMPONENT N-RECOGNIN 5; UBR5
*138480 - SOLUTE CARRIER FAMILY 25 (MITOCHONDRIAL CARRIER, FOLATE), MEMBER 32; SLC25A32
Cytogenetic locations: ## ###
#613077 - PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 5; PEOA5
*610635 - COLLAGEN TRIPLE-HELIX REPEAT-CONTAINING PROTEIN 1; CTHRC1
*606722 - NEUROCALCIN, DELTA; NCALD
Cytogenetic locations: #Q_z##
#618031 - CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 4; PPCD4
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