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#619824 - AGAMMAGLOBULINEMIA 8B, AUTOSOMAL RECESSIVE; AGM8B
Cytogenetic locations: 601697
Gene summaries Genetic tests Medical literature
#619182 - GASTRIC ADENOCARCINOMA AND PROXIMAL POLYPOSIS OF THE STOMACH; GAPPS
#617875 - POLYCYSTIC LIVER DISEASE 4 WITH OR WITHOUT KIDNEY CYSTS; PCLD4
Cytogenetic locations: #fLO##
#617572 - EXUDATIVE VITREORETINOPATHY 7; EVR7
Cytogenetic locations: 0#####
#616941 - AGAMMAGLOBULINEMIA 8A, AUTOSOMAL DOMINANT; AGM8A
#616724 - TOOTH AGENESIS, SELECTIVE, 7; STHAG7
#615221 - BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 16; BMND16
Cytogenetic locations: ###&##
#615220 - OSTEOGENESIS IMPERFECTA, TYPE XV; OI15
#615109 - COWDEN SYNDROME 6; CWS6
Cytogenetic locations: GSKIP
#615075 - NEURODEVELOPMENTAL DISORDER WITH SPASTIC DIPLEGIA AND VISUAL DEFECTS; NEDSDV
#613659 - GASTRIC CANCER
GASTRIC CANCER, INTESTINAL, INCLUDED
Cytogenetic locations: identified, mutation, 1p36, 602000, 1p36, 1p36, rs9303277, with, associated, 1p36
%613065 - LEUKEMIA, ACUTE LYMPHOBLASTIC; ALL
LEUKEMIA, ACUTE LYMPHOBLASTIC, SUSCEPTIBILITY TO, 1, INCLUDED
Cytogenetic locations: 1p36, 1p36, 1p36, 1p36.33, 1p36, 610259, 1p36, 1p36, 12q24.33
#612376 - ACUTE PROMYELOCYTIC LEUKEMIA; APL
Cytogenetic locations: 1p36, 1p36
*611731 - APC REGULATOR OF WNT SIGNALING PATHWAY; APC
Cytogenetic locations: 609497
#611528 - ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 12; ARVD12
Cytogenetic locations: Psmb3
#610947 - CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT 2; ADCAD2
Cytogenetic locations: ######
#608615 - OLIGODONTIA-COLORECTAL CANCER SYNDROME; ODCRCS
#607634 - OSTEOPETROSIS, AUTOSOMAL DOMINANT 1; OPTA1
*607343 - SAL-LIKE 4; SALL4
#607323 - DUANE-RADIAL RAY SYNDROME; DRRS
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