http://www.ncbi.nlm.nih.gov/htbin-post/Omim/getmorbid
MIM Morbid map Pubmed Nucleotide Protein Genome Structure Popset Taxonomy OMIM The OMIM Morbid Map presents the cytogenetic map location of disease genes described in OMIM. For a map organized by chromosome, see the OMIM Gene Map. For more refined maps of genes and DNA segments, use NCBI Entrez Map Viewer and the Genome Data_base. Search for: Enter gene symbol, chromosomal location, or disorder keyword to search for, e_g."recessive","CYP1","5","1pter",or"Xq"."You must capitalize X and Y to search for those chromosomes. Move Down Disorder Symbol (s) OMIM Location 3-Methylcrotonylglycinuria I (3) MCCC1, MCCA 210200 3q25-q27 3-Methylcrotonylglycinuria II (3) MCCC2, MCCB 210210 5q12-q13 3-beta-hydroxysteroid_dehydrogenase, type II, deficiency (3) HSD3B2 201810 1p13. 1 3-ketothiolase deficiency (3) ACAT1 203750 11q22.3-q23. 1 3-methylglutaconicaciduria, type III, 258501 (3) OPA3, MGA3 606580 19q13.2-q13. 3 3q21q26 syndrome (1) EVI1 165215 3q26 5-oxoprolinuria, 266130 (3) GSS, GSHS 601002 20q11.2 6-mercaptopurine sensitivity (3) TPMT 187680 6p22. 3 ABCD syndrome 600501 (3) EDNRB, HSCR2, ABCDS 131244 13q22 ACAT2 deficiency (1(?ACAT2 100678 6q25. 3-q26 ACTH deficiency (1) POMC 176830 2p23. 3 ACTH deficiency, 201400 (2) CRH 122560 8q13 ADULT syndrome, 103285 (3) TP63, KET , EEC3, SHFM4 603273 3q27 AGAT deficiency (3) GATM, AGAT 602360 15q15.3 Aarskog-Scott syndrome (3) FGD1, FGDY , AAS 305400 Xp11. 21 Abdominal obesity-metabolic syndrome (2) AOMS1, SYNX 605552 3q27 Abdominal obesity-metabolic syndrome, 605552 (2) AOMS2 605572 17p12 Abetalipoproteinemia (3) APOB , FLDB 107730 2p24 Abetalipoproteinemia, 200100 (3) MTP 157147 4q22-q24 Acampomelic campolelic dysplasia (3) SOX9, CMD1, SRA1 114290 17q24.3-q25. 1 Copyright 1966-2002 Johns_hopkins_university Move Down Disclaimer Write to the Help Desk Privacy Policy NCBI NLM NIH