OMIM QUERY RESULTS
                                       
   OMIM IRX Query: (wallace and d.)[rf]
   
    1. *141900 HEMOGLOBIN--BETA LOCUS [HBB; SICKLE CELL ANEMIA, INCLUDED;
       BETA-THALASSEMIAS, INCLUDED; HEINZ BODY ANEMIAS, BETA-GLOBIN TYPE,
       INCLUDED; METHEMOGLOBINEMIA, BETA-GLOBIN TYPE, INCLUDED;
       ERYTHREMIA, BETA-GLOBIN TYPE, INCLUDED; DYSERYTHROPOIETIC ANEMIA,
       CONGENITAL, IRISH OR WEATHERALL TYPE, INCLUDED]
    2. #535000 LEBER OPTIC ATROPHY [LEBER HEREDITARY OPTIC NEUROPATHY;
       LHON]
    3. *162200 NEUROFIBROMATOSIS [VON RECKLINGHAUSEN DISEASE;
       NEUROFIBROMATOSIS, TYPE I; NF1; NEUROFIBROMIN, INCLUDED]
    4. *176300 PREALBUMIN, THYROXINE-BINDING [TBPA; PALB; TRANSTHYRETIN;
       TTR; DYSPREALBUMINEMIC EUTHYROIDAL HYPERTHYROXINEMIA, INCLUDED;
       HYPERTHYROXINEMIA, DYSPREALBUMINEMIC, INCLUDED; HYPERTHYROXINEMIA,
       + DYSTRANSTHYRETINEMIC, INCLUDED; AMYLOID POLYNEUROPATHY, MULTIPLE
       + FORMS, INCLUDED; SENILE SYSTEMIC AMYLOIDOSIS, INCLUDED]
    5. *143100 HUNTINGTON DISEASE [HD; HUNTINGTON CHOREA; HUNTINGTIN,
       INCLUDED]
    6. *516003 COMPLEX I, SUBUNIT ND4 [MTND4; NADH-UBIQUINONE +
       OXIDOREDUCTASE, SUBUNIT ND4; NADH DEHYDROGENASE, SUBUNIT 4] + +
    7. *516040 COMPLEX IV, CYTOCHROME c OXIDASE SUBUNIT II [MTCO2; COII;
       + CYTOCHROME c OXIDASE II] + +
    8. *516000 COMPLEX I, SUBUNIT ND1 [MTND1; NADH-UBIQUINONE +
       OXIDOREDUCTASE, SUBUNIT ND1; NADH DEHYDROGENASE, SUBUNIT 1] + +
    9. *516030 COMPLEX IV, CYTOCHROME c OXIDASE SUBUNIT I [MTCO1; COI; +
       CYTOCHROME c OXIDASE I] + +
   10. *516006 COMPLEX I, SUBUNIT ND6 [MTND6; NADH-UBIQUINONE +
       OXIDOREDUCTASE, SUBUNIT ND6; NADH DEHYDROGENASE, SUBUNIT 6] + +
   11. *516002 COMPLEX I, SUBUNIT ND3 [MTND3; NADH-UBIQUINONE +
       OXIDOREDUCTASE, SUBUNIT ND3; NADH DEHYDROGENASE, SUBUNIT 3] + +
   12. *516005 COMPLEX I, SUBUNIT ND5 [MTND5; NADH-UBIQUINONE +
       OXIDOREDUCTASE, SUBUNIT ND5; NADH DEHYDROGENASE, SUBUNIT 5] + +
   13. *308000 HYPOXANTHINE GUANINE PHOSPHORIBOSYLTRANSFERASE [HPRT;
       HGPRT; LESCH-NYHAN SYNDROME, INCLUDED; LNS, INCLUDED]
   14. *219700 CYSTIC FIBROSIS [CF; CYSTIC FIBROSIS TRANSMEMBRANE
       CONDUCTANCE REGULATOR, INCLUDED; CFTR, INCLUDED; MUCOVISCIDOSIS]
   15. *516020 COMPLEX III, CYTOCHROME b SUBUNIT [CYTOCHROME b OF COMPLEX
       + III; MTCYB; UBIQUINONE-CYTOCHROME c OXIDOREDUCTASE, CYTOCHROME b
       + SUBUNIT] + +
   16. *305900 GLUCOSE-6-PHOSPHATE DEHYDROGENASE [G6PD]
   17. *107400 ANTITRYPSIN [ALPHA-1-ANTITRYPSIN; AAT; PROTEASE INHIBITOR;
       PI; ALPHA-1-ANTITRYPSIN DEFICIENCY, AUTOSOMAL RECESSIVE, INCLUDED]
   18. *516001 COMPLEX I, SUBUNIT ND2 [MTND2; NADH-UBIQUINONE +
       OXIDOREDUCTASE, SUBUNIT ND2; NADH DEHYDROGENASE, SUBUNIT 2] + +
   19. #104300 ALZHEIMER DISEASE [AD; AD1; PRESENILE AND SENILE DEMENTIA;
       ALZHEIMER DISEASE, FAMILIAL; FAD]
   20. *516050 COMPLEX IV, CYTOCHROME c OXIDASE SUBUNIT III [MTCO3;
       COIII; + CYTOCHROME c OXIDASE III] + +
   21. *516004 COMPLEX I, SUBUNIT ND4L [MTND4L; NADH-UBIQUINONE +
       OXIDOREDUCTASE, SUBUNIT ND4L; NADH DEHYDROGENASE, SUBUNIT 4L] + +
   22. *155600 MELANOMA, MALIGNANT [FAMILIAL ATYPICAL MOLE-MALIGNANT
       MELANOMA SYNDROME; FAMMM; FAMILIAL MELANOMA; MLM; DYSPLASTIC NEVUS
       SYNDROME, HEREDITARY; DNS, HEREDITARY; HEREDITARY CUTANEOUS
       MALIGNANT MELANOMA; HCMM; MELANOMA, CUTANEOUS MALIGNANT; CMM;
       CMM1; B-K MOLE + SYNDROME, INCLUDED]
   23. *301500 ANGIOKERATOMA, DIFFUSE [FABRY DISEASE; ANDERSON-FABRY
       DISEASE; HEREDITARY DYSTOPIC LIPIDOSIS; ALPHA-GALACTOSIDASE A
       DEFICIENCY; GLA DEFICIENCY; CERAMIDE TRIHEXOSIDASE DEFICIENCY]
   24. *173900 POLYCYSTIC KIDNEYS [ADULT POLYCYSTIC KIDNEY DISEASE; APKD;
       PKD; PKD1; POTTER TYPE III POLYCYSTIC KIDNEY DISEASE]
   25. G103600 ALBUMIN [ALB; DYSALBUMINEMIC HYPERTHYROXINEMIA, INCLUDED;
       HYPERTHYROXINEMIA, DYSALBUMINEMIC, INCLUDED; ANALBUMINEMIA,
       INCLUDED; BISALBUMINEMIA, INCLUDED]
   26. #100800 ACHONDROPLASIA [ACH]
   27. *247200 LISSENCEPHALY SYNDROME [MILLER-DIEKER LISSENCEPHALY
       SYNDROME; MDLS; MDS; MILLER-DIEKER SYNDROME CHROMOSOME REGION;
       MDCR; AGYRIA, INCLUDED; LIS1, INCLUDED; PLATELET-ACTIVATING FACTOR
       ACETYLHYDROLASE, INCLUDED; PAF ACETYLHYDROLASE, 45-KILODALTON
       SUBUNIT, INCLUDED]
   28. *103220 ADP/ATP TRANSLOCATOR OF SKELETAL MUSCLE [ADENINE
       NUCLEOTIDE TRANSLOCATOR-1; ANT; ANT1; ADP/ATP TRANSLOCASE-1]
   29. *300100 ADRENOLEUKODYSTROPHY [ALD; ADDISON DISEASE AND CEREBRAL
       SCLEROSIS; ADRENOMYELONEUROPATHY; AMN; SIEMERLING-CREUTZFELDT
       DISEASE; BRONZE SCHILDER'S DISEASE; MELANODERMIC LEUKODYSTROPHY;
       ADRENOLEUKODYSTROPHY PROTEIN, INCLUDED; ALDP, INCLUDED]
   30. *185500 SUPRAVALVAR AORTIC STENOSIS [SVAS; SUPRAVALVAR AORTIC
       STENOSIS, EISENBERG TYPE]
   31. *110300 BLOOD GROUP--ABO SYSTEM [ABO; ABO HISTO-BLOOD GROUP
       GLYCOSYLTRANSFERASES]
   32. #520000 DIABETES-DEAFNESS SYNDROME, MATERNALLY TRANSMITTED +
       [BALLINGER-WALLACE SYNDROME; DIABETES MELLITUS, TYPE II, WITH +
       DEAFNESS; NONINSULIN-DEPENDENT DIABETES MELLITUS WITH DEAFNESS;
       NIDDM + WITH DEAFNESS] + +
   33. *104170 ALPHA-GALACTOSIDASE B [GALB; N-ACETYL-ALPHA-D-
       GALACTOSAMINIDASE; NAGA; LYSOSOMAL ALPHA-N-ACETYLGALACTOSAMINIDASE
       DEFICIENCY, INCLUDED; SCHINDLER DISEASE, INCLUDED; NEUROAXONAL
       DYSTROPHY, SCHINDLER TYPE, INCLUDED; KANZAKI DISEASE, INCLUDED]
   34. *516060 COMPLEX V, ATP SYNTHASE, SUBUNIT ATPase 6 [MTATP6; ATP6] +
       +
   35. #545000 MERRF SYNDROME [MYOCLONUS EPILEPSY ASSOCIATED WITH
       RAGGED-RED + FIBERS] + +
   36. #515000 CHLORAMPHENICOL TOXICITY [ANEMIA, CHLORAMPHENICOL-INDUCED;
       + CHLORAMPHENICOL RESISTANCE, INCLUDED] + +
   37. *104200 ALPORT SYNDROME [HEREDITARY NEPHROPATHY AND DEAFNESS]
   38. *126380 DNA REPAIR DEFECT UV-20 OF CHINESE HAMSTER OVARY CELLS,
       COMPLEMENTATION OF [UV20; EXCISION-REPAIR, COMPLEMENTING
       DEFECTIVE, IN CHINESE HAMSTER, 1; ERCC1]
   39. #307000 HYDROCEPHALUS DUE TO CONGENITAL STENOSIS OF AQUEDUCT OF
       SYLVIUS [HSAS1; HSAS; HYCX; HYDROCEPHALUS, X-LINKED; AQUEDUCTAL
       STENOSIS, X-LINKED; XLAS]
   40. *590060 TRANSFER RNA, MITOCHONDRIAL, LYSINE [MTTK; tRNA-LYS, +
       MITOCHONDRIAL] + +
   41. *111700 BLOOD GROUP--RHESUS SYSTEM Cc/Ee POLYPEPTIDES [RHC; RHE;
       RHCE; RH-NULL HEMOLYTIC ANEMIA, INCLUDED]
   42. *303900 COLORBLINDNESS, PARTIAL, PROTAN SERIES [CBP; PROTANOPIA;
       RED COLORBLINDNESS; RED CONE PIGMENT, INCLUDED; RCP, INCLUDED]
   43. *106210 ANIRIDIA, TYPE II [AN2; PAIRED BOX HOMEOTIC GENE 6,
       INCLUDED; PAX6, INCLUDED]
   44. *102910 ADENOSINE TRIPHOSPHATE SYNTHASE, MITOCHONDRIAL, BETA
       SUBUNIT [ATP5B; ATPSB; ATPMB]
   45. *158380 MURINE MYELOID LEUKEMIA-ASSOCIATED GENE EVI-2, HUMAN
       HOMOLOG OF [EVI2; ECOTROPIC VIRAL INTEGRATION SITE 2A; EVI2A;
       EVDA]
   46. *252900 MUCOPOLYSACCHARIDOSIS TYPE IIIA [MPS IIIA; SANFILIPPO
       SYNDROME A; HEPARAN SULFATE SULFATASE DEFICIENCY]
       
Edit History

    1. 000004 EDITORIAL HISTORY 95/02/15 to 95/02/16
    2. 000011 EDITORIAL HISTORY 95/02/04 to 95/02/07
    3. 000045 EDITORIAL HISTORY 94/12/20 to 94/12/21
    4. 000046 EDITORIAL HISTORY 94/12/17 to 94/12/20   
   
   Total Hits: 50
   
   Your query produced more than 50 results.
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    GDB-OMIM