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#620427 - DYSTONIA 37, EARLY-ONSET, WITH STRIATAL LESIONS; DYT37
Cytogenetic locations: apparently
Gene summaries Genetic tests Medical literature
#620393 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 79; MRT79
Cytogenetic locations: pH#>##
*619998 - NUCLEOPORIN 42; NUP42
Cytogenetic locations: ######
#618804 - SANDESTIG-STEFANOVA SYNDROME; SANDSTEF
#618426 - ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 9; IIAE9
Cytogenetic locations: Lethal
#618393 - FETAL AKINESIA DEFORMATION SEQUENCE 4; FADS4
#618349 - GALLOWAY-MOWAT SYNDROME 8; GAMOS8
Cytogenetic locations: H3.4
#618348 - GALLOWAY-MOWAT SYNDROME 7; GAMOS7
Cytogenetic locations: `#u###
#618179 - MICROCEPHALY 24, PRIMARY, AUTOSOMAL RECESSIVE; MCPH24
Cytogenetic locations: 610142
#618178 - NEPHROTIC SYNDROME, TYPE 19; NPHS19
Cytogenetic locations: Seizures
#618177 - NEPHROTIC SYNDROME, TYPE 18; NPHS18
#618176 - NEPHROTIC SYNDROME, TYPE 17; NPHS17
#618078 - OVARIAN DYSGENESIS 6; ODG6
Cytogenetic locations: poZ###
#617184 - MITOCHONDRIAL DNA DEPLETION SYNDROME 12A (CARDIOMYOPATHIC TYPE), AUTOSOMAL DOMINANT; MTDPS12A
#616893 - NEPHROTIC SYNDROME, TYPE 13; NPHS13
Cytogenetic locations: 601500
#616892 - NEPHROTIC SYNDROME, TYPE 12; NPHS12
Cytogenetic locations: ##^###
#616730 - NEPHROTIC SYNDROME, TYPE 11; NPHS11
#615770 - ATRIAL FIBRILLATION, FAMILIAL, 15; ATFB15
*615754 - POM121 TRANSMEMBRANE NUCLEOPORIN C; POM121C
Cytogenetic locations: -
*615753 - POM121 TRANSMEMBRANE NUCLEOPORIN; POM121
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