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#620458 - AURICULOCONDYLAR SYNDROME 2B; ARCND2B
Cytogenetic locations: P##A##
Gene summaries Genetic tests Medical literature
#620111 - CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1J; CMT1J
Cytogenetic locations: #5#@##
#619538 - CEREBRAL CAVERNOUS MALFORMATIONS 4; CCM4
#619503 - NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND DYSMORPHIC FACIES; NEDHYDF
#619464 - SICK SINUS SYNDROME 4; SSS4
Cytogenetic locations: ######
#619363 - ANGIOEDEMA, HEREDITARY, 6; HAE6
Cytogenetic locations: p-t###
*619337 - NEUROMEDIN S; NMS
Cytogenetic locations: Cytochrome
#619290 - MAHVASH DISEASE; MVAH
Cytogenetic locations: 616375
#618961 - SPONDYLOMETAPHYSEAL DYSPLASIA WITH CORNEAL DYSTROPHY; SMDCD
Cytogenetic locations: B3gat3
#618825 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 63, WITH MACROCEPHALY; MRD63
Cytogenetic locations: Mitochondrial
#618573 - HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 7; CHNG7
#618534 - IMMUNODEFICIENCY 64 WITH LYMPHOPROLIFERATION; IMD64
*618134 - UROTENSIN 2B; UTS2B
Cytogenetic locations: 180647
#617691 - SPINOCEREBELLAR ATAXIA 44; SCA44
#617217 - AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA6; AI2A6
Cytogenetic locations: #tOz##
#617182 - LODDER-MERLA SYNDROME, TYPE 2, WITH DEVELOPMENTAL DELAY AND WITH OR WITHOUT CARDIAC ARRHYTHMIA; LDMLS2
#617173 - LODDER-MERLA SYNDROME, TYPE 1, WITH IMPAIRED INTELLECTUAL DEVELOPMENT AND CARDIAC ARRHYTHMIA; LDMLS1
#617061 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 44, WITH MICROCEPHALY; MRD44
#617024 - NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1H; CSNB1H
Cytogenetic locations: p#%###
#616973 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 42; MRD42
Cytogenetic locations: 1p36.33
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