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*516000 - COMPLEX I, SUBUNIT ND1; MTND1
MITOCHONDRIAL COMPLEX I DEFICIENCY, MITOCHONDRIAL TYPE 3, INCLUDED; MC1DM3, INCLUDED
Gene summaries Genetic tests Medical literature
*107730 - APOLIPOPROTEIN B; APOB
APOB100, INCLUDED
Cytogenetic locations: 605374
*516001 - COMPLEX I, SUBUNIT ND2; MTND2
#613659 - GASTRIC CANCER
GASTRIC CANCER, INTESTINAL, INCLUDED
Cytogenetic locations: 1p36, 1p36, 1p36, 1p36, 1p36, 1p36, 1p36, 1p36, 1p36, 1p36
#252650 - MUCOLIPIDOSIS IV; ML4
Cytogenetic locations: mutation
*516003 - COMPLEX I, SUBUNIT ND4; MTND4
*141900 - HEMOGLOBIN--BETA LOCUS; HBB
Cytogenetic locations: 16762915
*516005 - COMPLEX I, SUBUNIT ND5; MTND5
*142410 - HNF1 HOMEOBOX A; HNF1A
Cytogenetic locations: 11668618
*147440 - INSULIN-LIKE GROWTH FACTOR I; IGF1
Cytogenetic locations: between
*601545 - PLATELET-ACTIVATING FACTOR ACETYLHYDROLASE, ISOFORM 1B, ALPHA SUBUNIT; PAFAH1B1
Cytogenetic locations: 20675372
*603258 - INHIBITOR OF NUCLEAR FACTOR KAPPA-B KINASE, SUBUNIT BETA; IKBKB
Cytogenetic locations: 23636330
#535000 - LEBER OPTIC ATROPHY
#193300 - VON HIPPEL-LINDAU SYNDROME; VHLS
VON HIPPEL-LINDAU SYNDROME, MODIFIERS OF, INCLUDED
Cytogenetic locations: 1p36, 1p36
*116806 - CATENIN, BETA-1; CTNNB1
Cytogenetic locations: 20026746
+116790 - CATECHOL-O-METHYLTRANSFERASE; COMT
CATECHOL-O-METHYLTRANSFERASE ACTIVITY, LOW, IN RED CELLS, INCLUDED
Cytogenetic locations: 12595695
#168600 - PARKINSON DISEASE, LATE-ONSET; PD
Cytogenetic locations: 608821, 608821, 608821, 608821, 1p36, 1p36, 1p36
#142330 - HEPATIC ADENOMAS, FAMILIAL
Cytogenetic locations: 12207987
#269600 - SEA-BLUE HISTIOCYTE DISEASE
Cytogenetic locations: 180901
*610257 - SEC31 HOMOLOG A, COPII COAT COMPLEX COMPONENT; SEC31A
Cytogenetic locations: 10788476
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