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#620357 - DIARRHEA 13; DIAR13
Cytogenetic locations: #z####
Gene summaries Genetic tests Medical literature
#619338 - CATARACTS, SPASTIC PARAPARESIS, AND SPEECH DELAY; CSPSD
#619232 - BILE ACID CONJUGATION DEFECT 1; BACD1
Cytogenetic locations: 0t####
*619050 - 3-@HYDROXY-3-METHYLGLUTARYL-CoA LYASE-LIKE PROTEIN 1; HMGCLL1
#618960 - MITCHELL SYNDROME; MITCH
Cytogenetic locations: ##M###
#618598 - SPASTIC TETRAPLEGIA AND AXIAL HYPOTONIA, PROGRESSIVE; STAHP
Cytogenetic locations: ######
#618400 - CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2EE; CMT2EE
Cytogenetic locations: 606137
*618100 - MPV17 MITOCHONDRIAL INNER MEMBRANE PROTEIN-LIKE; MPV17L
#617917 - NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 8; NBIA8
*617399 - PEROXISOMAL MEMBRANE PROTEIN 2; PXMP2
#617370 - PEROXISOME BIOGENESIS DISORDER 10B; PBD10B
#617308 - BILE ACID SYNTHESIS DEFECT, CONGENITAL, 6; CBAS6
Cytogenetic locations: @^####
#616716 - RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 5; RCDP5
*616713 - PIPECOLIC ACID OXIDASE; PIPOX
Cytogenetic locations: #;#S##
#616617 - HEIMLER SYNDROME 2; HMLR2
*616397 - PEROXISOMAL MEMBRANE PROTEIN 4; PXMP4
Cytogenetic locations: #########(##
#616278 - BILE ACID SYNTHESIS DEFECT, CONGENITAL, 5; CBAS5
*616156 - FATTY ACYL CoA REDUCTASE 2; FAR2
#616154 - PEROXISOMAL FATTY ACYL-CoA REDUCTASE 1 DISORDER; PFCRD
Cytogenetic locations: @{#R##
*616133 - MPV17 MITOCHONDRIAL INNER MEMBRANE PROTEIN-LIKE 2; MPV17L2
Cytogenetic locations: ##########.#
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