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#620536 - ALPORT SYNDROME 3B, AUTOSOMAL RECESSIVE; ATS3B
Cytogenetic locations: ###x##
Gene summaries Genetic tests Medical literature
#620320 - HEMATURIA, BENIGN FAMILIAL, 2; BFH2
Cytogenetic locations: @!####
#620022 - STICKLER SYNDROME, TYPE VI; STL6
Cytogenetic locations: ######
#619817 - EPIDERMOLYSIS BULLOSA, JUNCTIONAL 6, WITH PYLORIC ATRESIA; JEB6
#619271 - BLEEDING DISORDER, PLATELET-TYPE, 24; BDPLT24
Cytogenetic locations: between
#619267 - GLANZMANN THROMBASTHENIA 2; GT2
#619161 - CARPAL TUNNEL SYNDROME 2; CTS2
Cytogenetic locations: @##M##
#618880 - GLAUCOMA, PRIMARY CLOSED-ANGLE; GLCC
Cytogenetic locations: 608365
#618824 - BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 8, AUTOSOMAL RECESSIVE; IBGC8
#618564 - MICROANGIOPATHY AND LEUKOENCEPHALOPATHY, PONTINE, AUTOSOMAL DOMINANT; PADMAL
#616914 - MARFANOID-PROGEROID-LIPODYSTROPHY SYNDROME; MFLS
Cytogenetic locations: #n]###
#616720 - MYASTHENIC SYNDROME, CONGENITAL, 19; CMS19
Cytogenetic locations: 116940
#616538 - MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 9; MDDGA9
Cytogenetic locations: mutation
#616221 - AMELOGENESIS IMPERFECTA, TYPE IH; AI1H
Cytogenetic locations: 601828
#616004 - DYSFIBRINOGENEMIA, CONGENITAL
HYPODYSFIBRINOGENEMIA, CONGENITAL, INCLUDED
Cytogenetic locations: 1p36, 1p36, 1p36
#615629 - DEAFNESS, AUTOSOMAL DOMINANT 56; DFNA56
Cytogenetic locations: 604574
#615120 - MYASTHENIC SYNDROME, CONGENITAL, 8; CMS8
Cytogenetic locations: 1p36.33
#614748 - EPIDERMOLYSIS BULLOSA, JUNCTIONAL 7, WITH INTERSTITIAL LUNG DISEASE AND NEPHROTIC SYNDROME; JEB7
#614519 - HEMORRHAGE, INTRACEREBRAL, SUSCEPTIBILITY TO; ICH
Cytogenetic locations: 609678, 609678, 1p36
#614483 - BRAIN SMALL VESSEL DISEASE 2; BSVD2
Cytogenetic locations: 609678
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