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#620705 - SPERMATOGENIC FAILURE 89; SPGF89
Gene summaries Genetic tests Medical literature
#620675 - LEUKODYSTROPHY, HYPOMYELINATING, 27; HLD27
#620647 - PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 6; PEOB6
*620063 - DNA POLYMERASE ALPHA-2, ACCESSORY SUBUNIT; POLA2
*620041 - 5-PRIME-@NUCLEOTIDASE, CYTOSOLIC IIIB; NT5C3B
Cytogenetic locations: 17q12
#620005 - PRIMORDIAL DWARFISM-IMMUNODEFICIENCY-LIPODYSTROPHY SYNDROME; PDIL
Cytogenetic locations: Ectodermal
#619872 - IMMUNODEFICIENCY 101 (VARICELLA ZOSTER VIRUS-SPECIFIC); IMD101
#619859 - PHOSPHORIBOSYLAMINOIMIDAZOLE CARBOXYLASE DEFICIENCY; PAICSD
Cytogenetic locations: ##9###
#619844 - INTELLECTUAL DEVELOPMENTAL DISORDER WITH OR WITHOUT PERIPHERAL NEUROPATHY; IDDPN
*619801 - RNA POLYMERASE III, SUBUNIT H; POLR3H
Cytogenetic locations: ###########
#619742 - CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1I; CMT1I
#619651 - NEURODEVELOPMENTAL DISORDER WITH HYPERKINETIC MOVEMENTS AND DYSKINESIA; NEDHYD
Cytogenetic locations: 601199
#619647 - DYSKINESIA WITH OROFACIAL INVOLVEMENT, AUTOSOMAL RECESSIVE; DSKOR
*619357 - ADENYLATE KINASE 6; AK6
#619310 - LEUKODYSTROPHY, HYPOMYELINATING, 21; HLD21
Cytogenetic locations: #p#D##
#619234 - SHORT STATURE, OLIGODONTIA, DYSMORPHIC FACIES, AND MOTOR DELAY; SOFM
Cytogenetic locations: #{####
#619150 - INTELLECTUAL DEVELOPMENTAL DISORDER WITH PAROXYSMAL DYSKINESIA OR SEIZURES; IDDPADS
Cytogenetic locations: 600466
#618939 - TREACHER COLLINS SYNDROME 4; TCS4
Cytogenetic locations: 602452
#618603 - NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND VARIABLE INTELLECTUAL AND BEHAVIORAL ABNORMALITIES; NEDHIB
#618555 - NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE1I; CSNB1I
Cytogenetic locations: `9####
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