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#616625 - CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2W; CMT2W
Cytogenetic locations: 22930593
Gene summaries Genetic tests Medical literature
*614843 - ODONTOGENIC AMELOBLAST-ASSOCIATED PROTEIN; ODAM
Cytogenetic locations: 14647039
*614506 - BRCA1-ASSOCIATED ATM ACTIVATOR 1; BRAT1
Cytogenetic locations: 26535877
#614504 - USHER SYNDROME, TYPE IIIB; USH3B
Cytogenetic locations: 22279524
#614501 - NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, CRANIOFACIAL ABNORMALITIES, AND SEIZURES; NEDHCS
#614499 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 34, WITH VARIANT LISSENCEPHALY; MRT34
Cytogenetic locations: 606523
#614498 - RIGIDITY AND MULTIFOCAL SEIZURE SYNDROME, LETHAL NEONATAL; RMFSL
#613135 - PARKINSONISM-DYSTONIA 1, INFANTILE-ONSET; PKDYS1
*610053 - TUBULIN-GAMMA COMPLEX-ASSOCIATED PROTEIN 6; TUBGCP6
*609584 - L-2-HYDROXYGLUTARATE DEHYDROGENASE; L2HGDH
Cytogenetic locations: 19911013
*609144 - FLVCR HEME TRANSPORTER 1; FLVCR1
Cytogenetic locations: 603305
#609033 - POSTERIOR COLUMN ATAXIA WITH RETINITIS PIGMENTOSA; AXPC1
*608241 - SMAD NUCLEAR INTERACTING PROTEIN 1; SNIP1
*603454 - CASP2 AND RIPK1 DOMAIN-CONTAINING ADAPTOR WITH DEATH DOMAIN; CRADD
*600783 - HISTIDYL-tRNA SYNTHETASE 2; HARS2
Cytogenetic locations: 31486067
*300647 - APC MEMBRANE RECRUITMENT PROTEIN 1; AMER1
Cytogenetic locations: 19383023
#251270 - MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 1; MCCRP1
Cytogenetic locations: 17486591
*142810 - HISTIDYL-tRNA SYNTHETASE 1; HARS1
Cytogenetic locations: 23464104
*126455 - SOLUTE CARRIER FAMILY 6 (NEUROTRANSMITTER TRANSPORTER, DOPAMINE), MEMBER 3; SLC6A3
Cytogenetic locations: 17690258
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