From: <cmu...@us...> - 2009-10-20 22:10:32
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Revision: 2863 http://obo.svn.sourceforge.net/obo/?rev=2863&view=rev Author: cmungall Date: 2009-10-20 22:10:19 +0000 (Tue, 20 Oct 2009) Log Message: ----------- Added Paths: ----------- phenotype-commons/annotations/OMIM/by-disease/MIM-600002.tab phenotype-commons/annotations/OMIM/by-disease/MIM-600059.tab phenotype-commons/annotations/OMIM/by-disease/MIM-600060.tab phenotype-commons/annotations/OMIM/by-disease/MIM-600072.tab phenotype-commons/annotations/OMIM/by-disease/MIM-600081.tab phenotype-commons/annotations/OMIM/by-disease/MIM-600101.tab phenotype-commons/annotations/OMIM/by-disease/MIM-600105.tab phenotype-commons/annotations/OMIM/by-disease/MIM-600110.tab phenotype-commons/annotations/OMIM/by-disease/MIM-600116.tab phenotype-commons/annotations/OMIM/by-disease/MIM-600118.tab phenotype-commons/annotations/OMIM/by-disease/MIM-600121.tab phenotype-commons/annotations/OMIM/by-disease/MIM-600132.tab phenotype-commons/annotations/OMIM/by-disease/MIM-600138.tab 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phenotype-commons/annotations/OMIM/by-disease/MIM-608716.tab phenotype-commons/annotations/OMIM/by-disease/MIM-608728.tab phenotype-commons/annotations/OMIM/by-disease/MIM-608747.tab phenotype-commons/annotations/OMIM/by-disease/MIM-608768.tab phenotype-commons/annotations/OMIM/by-disease/MIM-608782.tab phenotype-commons/annotations/OMIM/by-disease/MIM-608799.tab phenotype-commons/annotations/OMIM/by-disease/MIM-608800.tab phenotype-commons/annotations/OMIM/by-disease/MIM-608804.tab phenotype-commons/annotations/OMIM/by-disease/MIM-608807.tab phenotype-commons/annotations/OMIM/by-disease/MIM-608810.tab phenotype-commons/annotations/OMIM/by-disease/MIM-608836.tab phenotype-commons/annotations/OMIM/by-disease/MIM-608840.tab phenotype-commons/annotations/OMIM/by-disease/MIM-608864.tab phenotype-commons/annotations/OMIM/by-disease/MIM-608902.tab phenotype-commons/annotations/OMIM/by-disease/MIM-608930.tab phenotype-commons/annotations/OMIM/by-disease/MIM-608931.tab phenotype-commons/annotations/OMIM/by-disease/MIM-608957.tab phenotype-commons/annotations/OMIM/by-disease/MIM-609015.tab phenotype-commons/annotations/OMIM/by-disease/MIM-609040.tab phenotype-commons/annotations/OMIM/by-disease/MIM-609048.tab phenotype-commons/annotations/OMIM/by-disease/MIM-609049.tab phenotype-commons/annotations/OMIM/by-disease/MIM-609056.tab phenotype-commons/annotations/OMIM/by-disease/MIM-609060.tab phenotype-commons/annotations/OMIM/by-disease/MIM-609136.tab phenotype-commons/annotations/OMIM/by-disease/MIM-609152.tab phenotype-commons/annotations/OMIM/by-disease/MIM-609192.tab phenotype-commons/annotations/OMIM/by-disease/MIM-609200.tab phenotype-commons/annotations/OMIM/by-disease/MIM-609220.tab phenotype-commons/annotations/OMIM/by-disease/MIM-609227.tab phenotype-commons/annotations/OMIM/by-disease/MIM-609241.tab phenotype-commons/annotations/OMIM/by-disease/MIM-609242.tab phenotype-commons/annotations/OMIM/by-disease/MIM-609254.tab phenotype-commons/annotations/OMIM/by-disease/MIM-609260.tab phenotype-commons/annotations/OMIM/by-disease/MIM-609284.tab phenotype-commons/annotations/OMIM/by-disease/MIM-609286.tab phenotype-commons/annotations/OMIM/by-disease/MIM-609304.tab phenotype-commons/annotations/OMIM/by-disease/MIM-609307.tab phenotype-commons/annotations/OMIM/by-disease/MIM-609308.tab phenotype-commons/annotations/OMIM/by-disease/MIM-609311.tab phenotype-commons/annotations/OMIM/by-disease/MIM-609441.tab phenotype-commons/annotations/OMIM/by-disease/MIM-609446.tab phenotype-commons/annotations/OMIM/by-disease/MIM-609452.tab phenotype-commons/annotations/OMIM/by-disease/MIM-609460.tab phenotype-commons/annotations/OMIM/by-disease/MIM-609524.tab phenotype-commons/annotations/OMIM/by-disease/MIM-609528.tab phenotype-commons/annotations/OMIM/by-disease/MIM-609533.tab phenotype-commons/annotations/OMIM/by-disease/MIM-609560.tab phenotype-commons/annotations/OMIM/by-disease/MIM-609583.tab phenotype-commons/annotations/OMIM/by-disease/MIM-609597.tab phenotype-commons/annotations/OMIM/by-disease/MIM-609634.tab phenotype-commons/annotations/OMIM/by-disease/MIM-609638.tab phenotype-commons/annotations/OMIM/by-disease/MIM-609796.tab phenotype-commons/annotations/OMIM/by-disease/MIM-609814.tab phenotype-commons/annotations/OMIM/by-disease/MIM-609820.tab phenotype-commons/annotations/OMIM/by-disease/MIM-609821.tab phenotype-commons/annotations/OMIM/by-disease/MIM-609823.tab phenotype-commons/annotations/OMIM/by-disease/MIM-609924.tab phenotype-commons/annotations/OMIM/by-disease/MIM-609968.tab phenotype-commons/annotations/OMIM/by-disease/MIM-609975.tab phenotype-commons/annotations/OMIM/by-disease/MIM-610003.tab phenotype-commons/annotations/OMIM/by-disease/MIM-610006.tab phenotype-commons/annotations/OMIM/by-disease/MIM-610021.tab phenotype-commons/annotations/OMIM/by-disease/MIM-610031.tab phenotype-commons/annotations/OMIM/by-disease/MIM-610090.tab phenotype-commons/annotations/OMIM/by-disease/MIM-610127.tab phenotype-commons/annotations/OMIM/by-disease/MIM-610153.tab phenotype-commons/annotations/OMIM/by-disease/MIM-610188.tab phenotype-commons/annotations/OMIM/by-disease/MIM-610189.tab phenotype-commons/annotations/OMIM/by-disease/MIM-610193.tab phenotype-commons/annotations/OMIM/by-disease/MIM-610198.tab phenotype-commons/annotations/OMIM/by-disease/MIM-610202.tab phenotype-commons/annotations/OMIM/by-disease/MIM-610253.tab phenotype-commons/annotations/OMIM/by-disease/MIM-610256.tab phenotype-commons/annotations/OMIM/by-disease/MIM-610313.tab phenotype-commons/annotations/OMIM/by-disease/MIM-610370.tab phenotype-commons/annotations/OMIM/by-disease/MIM-610377.tab phenotype-commons/annotations/OMIM/by-disease/MIM-610448.tab phenotype-commons/annotations/OMIM/by-disease/MIM-610455.tab phenotype-commons/annotations/OMIM/by-disease/MIM-610460.tab phenotype-commons/annotations/OMIM/by-disease/MIM-610474.tab phenotype-commons/annotations/OMIM/by-disease/MIM-610475.tab phenotype-commons/annotations/OMIM/by-disease/MIM-610476.tab phenotype-commons/annotations/OMIM/by-disease/MIM-610489.tab phenotype-commons/annotations/OMIM/by-disease/MIM-610498.tab phenotype-commons/annotations/OMIM/by-disease/MIM-610505.tab phenotype-commons/annotations/OMIM/by-disease/MIM-610532.tab phenotype-commons/annotations/OMIM/by-disease/MIM-610600.tab phenotype-commons/annotations/OMIM/by-disease/MIM-610651.tab phenotype-commons/annotations/OMIM/by-disease/MIM-610682.tab phenotype-commons/annotations/OMIM/by-disease/MIM-610688.tab phenotype-commons/annotations/OMIM/by-disease/MIM-610706.tab phenotype-commons/annotations/OMIM/by-disease/MIM-610725.tab phenotype-commons/annotations/OMIM/by-disease/MIM-610755.tab phenotype-commons/annotations/OMIM/by-disease/MIM-610765.tab phenotype-commons/annotations/OMIM/by-disease/MIM-610768.tab phenotype-commons/annotations/OMIM/by-disease/MIM-610798.tab phenotype-commons/annotations/OMIM/by-disease/MIM-610854.tab phenotype-commons/annotations/OMIM/by-disease/MIM-610915.tab phenotype-commons/annotations/OMIM/by-disease/MIM-610951.tab phenotype-commons/annotations/OMIM/by-disease/MIM-610978.tab phenotype-commons/annotations/OMIM/by-disease/MIM-610984.tab phenotype-commons/annotations/OMIM/by-disease/MIM-610992.tab phenotype-commons/annotations/OMIM/by-disease/MIM-611022.tab phenotype-commons/annotations/OMIM/by-disease/MIM-611038.tab phenotype-commons/annotations/OMIM/by-disease/MIM-611040.tab phenotype-commons/annotations/OMIM/by-disease/MIM-611067.tab phenotype-commons/annotations/OMIM/by-disease/MIM-611126.tab phenotype-commons/annotations/OMIM/by-disease/MIM-611131.tab phenotype-commons/annotations/OMIM/by-disease/MIM-611377.tab phenotype-commons/annotations/OMIM/by-disease/MIM-611489.tab phenotype-commons/annotations/OMIM/by-disease/MIM-611528.tab phenotype-commons/annotations/OMIM/by-disease/MIM-611561.tab phenotype-commons/annotations/OMIM/by-disease/MIM-611588.tab phenotype-commons/annotations/OMIM/by-disease/MIM-611597.tab phenotype-commons/annotations/OMIM/by-disease/MIM-611603.tab phenotype-commons/annotations/OMIM/by-disease/MIM-611615.tab phenotype-commons/annotations/OMIM/by-disease/MIM-611638.tab phenotype-commons/annotations/OMIM/by-disease/MIM-611705.tab phenotype-commons/annotations/OMIM/by-disease/MIM-611719.tab phenotype-commons/annotations/OMIM/by-disease/MIM-611721.tab phenotype-commons/annotations/OMIM/by-disease/MIM-611722.tab phenotype-commons/annotations/OMIM/by-disease/MIM-611726.tab phenotype-commons/annotations/OMIM/by-disease/MIM-612124.tab phenotype-commons/annotations/OMIM/by-disease/MIM-612201.tab phenotype-commons/annotations/OMIM/by-disease/MIM-612227.tab phenotype-commons/annotations/OMIM/by-disease/MIM-612233.tab phenotype-commons/annotations/OMIM/by-disease/MIM-612290.tab Added: phenotype-commons/annotations/OMIM/by-disease/MIM-600002.tab =================================================================== --- phenotype-commons/annotations/OMIM/by-disease/MIM-600002.tab (rev 0) +++ phenotype-commons/annotations/OMIM/by-disease/MIM-600002.tab 2009-10-20 22:10:19 UTC (rev 2863) @@ -0,0 +1,3 @@ +Disease ID Disease Name Gene ID Gene Name Genotype Gene Symbol(s) Phenotype ID Phenotype Name Entity ID Entity Name Quality ID Quality Name Add'l Entity ID Add 'l Entity Name Mode of inheritance ID Mode of inheritance Name Age of Onset ID Age of Onset Name Frequency Abnormal ID Abnormal Name Description Orthologs Pub Date Created +MIM:600002 MIM:168468 PTH1R HP:0000007 +MIM:600002 MIM:168468 PTH1R HP:0002652 FMA:23875 PATO:0000640 Added: phenotype-commons/annotations/OMIM/by-disease/MIM-600059.tab =================================================================== --- phenotype-commons/annotations/OMIM/by-disease/MIM-600059.tab (rev 0) +++ phenotype-commons/annotations/OMIM/by-disease/MIM-600059.tab 2009-10-20 22:10:19 UTC (rev 2863) @@ -0,0 +1,6 @@ +Disease ID Disease Name Gene ID Gene Name Genotype Gene Symbol(s) Phenotype ID Phenotype Name Entity ID Entity Name Quality ID Quality Name Add'l Entity ID Add 'l Entity Name Mode of inheritance ID Mode of inheritance Name Age of Onset ID Age of Onset Name Frequency Abnormal ID Abnormal Name Description Orthologs Pub Date Created +MIM:600059 MIM:607300 PRPF8 HP:0000006 +MIM:600059 MIM:607300 PRPF8 HP:0000546 FMA:58301 PATO:0000639 +MIM:600059 MIM:607300 PRPF8 HP:0000662 +MIM:600059 MIM:607300 PRPF8 HP:0001133 +MIM:600059 MIM:607300 PRPF8 HP:0007645 Added: phenotype-commons/annotations/OMIM/by-disease/MIM-600060.tab =================================================================== --- phenotype-commons/annotations/OMIM/by-disease/MIM-600060.tab (rev 0) +++ phenotype-commons/annotations/OMIM/by-disease/MIM-600060.tab 2009-10-20 22:10:19 UTC (rev 2863) @@ -0,0 +1,10 @@ +Disease ID Disease Name Gene ID Gene Name Genotype Gene Symbol(s) Phenotype ID Phenotype Name Entity ID Entity Name Quality ID Quality Name Add'l Entity ID Add 'l Entity Name Mode of inheritance ID Mode of inheritance Name Age of Onset ID Age of Onset Name Frequency Abnormal ID Abnormal Name Description Orthologs Pub Date Created +MIM:600060 MIM:276903 MYO7A HP:0000007 +MIM:600060 MIM:276903 MYO7A HP:0000404 GO:0007605 PATO:0000462 +MIM:600060 MIM:276903 MYO7A HP:0001455 +MIM:600060 MIM:276903 MYO7A HP:0001751 FMA:7193 PATO:0001641 +MIM:600060 MIM:276903 MYO7A HP:0002321 +MIM:600060 MIM:276903 MYO7A HP:0003577 +MIM:600060 MIM:276903 MYO7A HP:0003618 +MIM:600060 MIM:276903 MYO7A HP:0008513 +MIM:600060 MIM:276903 MYO7A HP:0008530 Added: phenotype-commons/annotations/OMIM/by-disease/MIM-600072.tab =================================================================== --- phenotype-commons/annotations/OMIM/by-disease/MIM-600072.tab (rev 0) +++ phenotype-commons/annotations/OMIM/by-disease/MIM-600072.tab 2009-10-20 22:10:19 UTC (rev 2863) @@ -0,0 +1,17 @@ +Disease ID Disease Name Gene ID Gene Name Genotype Gene Symbol(s) Phenotype ID Phenotype Name Entity ID Entity Name Quality ID Quality Name Add'l Entity ID Add 'l Entity Name Mode of inheritance ID Mode of inheritance Name Age of Onset ID Age of Onset Name Frequency Abnormal ID Abnormal Name Description Orthologs Pub Date Created +MIM:600072 MIM:176640 PRNP HP:0000006 +MIM:600072 MIM:176640 PRNP HP:0000016 +MIM:600072 MIM:176640 PRNP HP:0000651 +MIM:600072 MIM:176640 PRNP HP:0000726 +MIM:600072 MIM:176640 PRNP HP:0001064 +MIM:600072 MIM:176640 PRNP HP:0001251 GO:0050881 PATO:0000770 +MIM:600072 MIM:176640 PRNP HP:0001260 +MIM:600072 MIM:176640 PRNP HP:0001336 +MIM:600072 MIM:176640 PRNP HP:0001824 +MIM:600072 MIM:176640 PRNP HP:0001945 +MIM:600072 MIM:176640 PRNP HP:0002015 GO:0043050 PATO:0001641 +MIM:600072 MIM:176640 PRNP HP:0002019 GO:0030421 PATO:0000381 +MIM:600072 MIM:176640 PRNP HP:0002400 +MIM:600072 MIM:176640 PRNP HP:0002459 +MIM:600072 MIM:176640 PRNP HP:0003581 +MIM:600072 MIM:176640 PRNP HP:0005936 Added: phenotype-commons/annotations/OMIM/by-disease/MIM-600081.tab =================================================================== --- phenotype-commons/annotations/OMIM/by-disease/MIM-600081.tab (rev 0) +++ phenotype-commons/annotations/OMIM/by-disease/MIM-600081.tab 2009-10-20 22:10:19 UTC (rev 2863) @@ -0,0 +1,27 @@ +Disease ID Disease Name Gene ID Gene Name Genotype Gene Symbol(s) Phenotype ID Phenotype Name Entity ID Entity Name Quality ID Quality Name Add'l Entity ID Add 'l Entity Name Mode of inheritance ID Mode of inheritance Name Age of Onset ID Age of Onset Name Frequency Abnormal ID Abnormal Name Description Orthologs Pub Date Created +MIM:600081 MIM:608713 CYP2R1 HP:0000007 +MIM:600081 MIM:608713 CYP2R1 HP:0000254 FMA:63864 PATO:0000001 +MIM:600081 MIM:608713 CYP2R1 HP:0000886 FMA:7480 PATO:0001617 +MIM:600081 MIM:608713 CYP2R1 HP:0001252 FMA:30316 PATO:0001619 PATO:0001869 +MIM:600081 MIM:608713 CYP2R1 HP:0001324 FMA:5022 PATO:0001779 +MIM:600081 MIM:608713 CYP2R1 HP:0001508 +MIM:600081 MIM:608713 CYP2R1 HP:0002148 FMA:62970 PATO:0001163 CHEBI:26020 +MIM:600081 MIM:608713 CYP2R1 HP:0002355 +MIM:600081 MIM:608713 CYP2R1 HP:0002653 +MIM:600081 MIM:608713 CYP2R1 HP:0002660 HP:0002662 PATO:0002051 +MIM:600081 MIM:608713 CYP2R1 HP:0002663 GO:0001503 PATO:0000502 +MIM:600081 MIM:608713 CYP2R1 HP:0002748 +MIM:600081 MIM:608713 CYP2R1 HP:0002752 +MIM:600081 MIM:608713 CYP2R1 HP:0002753 FMA:24018 PATO:0000592 +MIM:600081 MIM:608713 CYP2R1 HP:0002976 +MIM:600081 MIM:608713 CYP2R1 HP:0002979 FMA:24979 PATO:0000406 +MIM:600081 MIM:608713 CYP2R1 HP:0003013 +MIM:600081 MIM:608713 CYP2R1 HP:0003017 +MIM:600081 MIM:608713 CYP2R1 HP:0003018 PATO:0000001 +MIM:600081 MIM:608713 CYP2R1 HP:0003020 +MIM:600081 MIM:608713 CYP2R1 HP:0003029 +MIM:600081 MIM:608713 CYP2R1 HP:0003155 +MIM:600081 MIM:608713 CYP2R1 HP:0003576 +MIM:600081 MIM:608713 CYP2R1 HP:0003698 +MIM:600081 MIM:608713 CYP2R1 HP:0004492 +MIM:600081 MIM:608713 CYP2R1 HP:0006620 Added: phenotype-commons/annotations/OMIM/by-disease/MIM-600101.tab =================================================================== --- phenotype-commons/annotations/OMIM/by-disease/MIM-600101.tab (rev 0) +++ phenotype-commons/annotations/OMIM/by-disease/MIM-600101.tab 2009-10-20 22:10:19 UTC (rev 2863) @@ -0,0 +1,5 @@ +Disease ID Disease Name Gene ID Gene Name Genotype Gene Symbol(s) Phenotype ID Phenotype Name Entity ID Entity Name Quality ID Quality Name Add'l Entity ID Add 'l Entity Name Mode of inheritance ID Mode of inheritance Name Age of Onset ID Age of Onset Name Frequency Abnormal ID Abnormal Name Description Orthologs Pub Date Created +MIM:600101 MIM:603537 KCNQ4 HP:0000006 +MIM:600101 MIM:603537 KCNQ4 HP:0000404 GO:0007605 PATO:0000462 +MIM:600101 MIM:603537 KCNQ4 HP:0008513 +MIM:600101 MIM:603537 KCNQ4 HP:0008530 Added: phenotype-commons/annotations/OMIM/by-disease/MIM-600105.tab =================================================================== --- phenotype-commons/annotations/OMIM/by-disease/MIM-600105.tab (rev 0) +++ phenotype-commons/annotations/OMIM/by-disease/MIM-600105.tab 2009-10-20 22:10:19 UTC (rev 2863) @@ -0,0 +1,3 @@ +Disease ID Disease Name Gene ID Gene Name Genotype Gene Symbol(s) Phenotype ID Phenotype Name Entity ID Entity Name Quality ID Quality Name Add'l Entity ID Add 'l Entity Name Mode of inheritance ID Mode of inheritance Name Age of Onset ID Age of Onset Name Frequency Abnormal ID Abnormal Name Description Orthologs Pub Date Created +MIM:600105 MIM:604210 CRB1 HP:0000007 +MIM:600105 MIM:604210 CRB1 HP:0000510 Added: phenotype-commons/annotations/OMIM/by-disease/MIM-600110.tab =================================================================== --- phenotype-commons/annotations/OMIM/by-disease/MIM-600110.tab (rev 0) +++ phenotype-commons/annotations/OMIM/by-disease/MIM-600110.tab 2009-10-20 22:10:19 UTC (rev 2863) @@ -0,0 +1,6 @@ +Disease ID Disease Name Gene ID Gene Name Genotype Gene Symbol(s) Phenotype ID Phenotype Name Entity ID Entity Name Quality ID Quality Name Add'l Entity ID Add 'l Entity Name Mode of inheritance ID Mode of inheritance Name Age of Onset ID Age of Onset Name Frequency Abnormal ID Abnormal Name Description Orthologs Pub Date Created +MIM:600110 MIM:605512 ELOVL4 HP:0000007 +MIM:600110 MIM:605512 ELOVL4 HP:0000505 GO:0007601 PATO:0000762 +MIM:600110 MIM:605512 ELOVL4 HP:0000603 FMA:30328 HP:0000575 +MIM:600110 MIM:605512 ELOVL4 HP:0001455 +MIM:600110 MIM:605512 ELOVL4 HP:0007914 Added: phenotype-commons/annotations/OMIM/by-disease/MIM-600116.tab =================================================================== --- phenotype-commons/annotations/OMIM/by-disease/MIM-600116.tab (rev 0) +++ phenotype-commons/annotations/OMIM/by-disease/MIM-600116.tab 2009-10-20 22:10:19 UTC (rev 2863) @@ -0,0 +1,14 @@ +Disease ID Disease Name Gene ID Gene Name Genotype Gene Symbol(s) Phenotype ID Phenotype Name Entity ID Entity Name Quality ID Quality Name Add'l Entity ID Add 'l Entity Name Mode of inheritance ID Mode of inheritance Name Age of Onset ID Age of Onset Name Frequency Abnormal ID Abnormal Name Description Orthologs Pub Date Created +MIM:600116 MIM:602544 PARK2 HP:0000007 +MIM:600116 MIM:602544 PARK2 HP:0001288 +MIM:600116 MIM:602544 PARK2 HP:0001300 +MIM:600116 MIM:602544 PARK2 HP:0001332 FMA:30316 PATO:0001814 +MIM:600116 MIM:602544 PARK2 HP:0001337 +MIM:600116 MIM:602544 PARK2 HP:0002063 +MIM:600116 MIM:602544 PARK2 HP:0002067 +MIM:600116 MIM:602544 PARK2 HP:0002171 FMA:55675 PATO:0002002 FMA:54537 +MIM:600116 MIM:602544 PARK2 HP:0002172 +MIM:600116 MIM:602544 PARK2 HP:0002400 +MIM:600116 MIM:602544 PARK2 HP:0003598 +MIM:600116 MIM:602544 PARK2 HP:0003667 +MIM:600116 MIM:602544 PARK2 HP:0007184 Added: phenotype-commons/annotations/OMIM/by-disease/MIM-600118.tab =================================================================== --- phenotype-commons/annotations/OMIM/by-disease/MIM-600118.tab (rev 0) +++ phenotype-commons/annotations/OMIM/by-disease/MIM-600118.tab 2009-10-20 22:10:19 UTC (rev 2863) @@ -0,0 +1,23 @@ +Disease ID Disease Name Gene ID Gene Name Genotype Gene Symbol(s) Phenotype ID Phenotype Name Entity ID Entity Name Quality ID Quality Name Add'l Entity ID Add 'l Entity Name Mode of inheritance ID Mode of inheritance Name Age of Onset ID Age of Onset Name Frequency Abnormal ID Abnormal Name Description Orthologs Pub Date Created +MIM:600118 MIM:602536 RAB3GAP1 HP:0000007 +MIM:600118 MIM:602536 RAB3GAP1 HP:0000028 +MIM:600118 MIM:602536 RAB3GAP1 HP:0000252 FMA:46565 PATO:0000587 +MIM:600118 MIM:602536 RAB3GAP1 HP:0000400 FMA:52781 PATO:0000586 +MIM:600118 MIM:602536 RAB3GAP1 HP:0000482 FMA:58238 PATO:0000587 +MIM:600118 MIM:602536 RAB3GAP1 HP:0000508 +MIM:600118 MIM:602536 RAB3GAP1 HP:0000519 +MIM:600118 MIM:602536 RAB3GAP1 HP:0000568 +MIM:600118 MIM:602536 RAB3GAP1 HP:0000648 FMA:50863 PATO:0001623 +MIM:600118 MIM:602536 RAB3GAP1 HP:0000939 _:increased_bone_resorption_and__:decreased_osteogenesis PATO:0001869 +MIM:600118 MIM:602536 RAB3GAP1 HP:0001249 +MIM:600118 MIM:602536 RAB3GAP1 HP:0001252 FMA:30316 PATO:0001619 PATO:0001869 +MIM:600118 MIM:602536 RAB3GAP1 HP:0001264 +MIM:600118 MIM:602536 RAB3GAP1 HP:0001274 PATO:0001557 FMA:86464 +MIM:600118 MIM:602536 RAB3GAP1 HP:0001347 +MIM:600118 MIM:602536 RAB3GAP1 HP:0001509 FMA:20394 PATO:0000569 +MIM:600118 MIM:602536 RAB3GAP1 HP:0002059 +MIM:600118 MIM:602536 RAB3GAP1 HP:0002079 FMA:86464 PATO:0000645 +MIM:600118 MIM:602536 RAB3GAP1 HP:0002219 FMA:24728 HP:0000998 +MIM:600118 MIM:602536 RAB3GAP1 HP:0002751 PATO:0000001 +MIM:600118 MIM:602536 RAB3GAP1 HP:0003241 +MIM:600118 MIM:602536 RAB3GAP1 HP:0008916 Added: phenotype-commons/annotations/OMIM/by-disease/MIM-600121.tab =================================================================== --- phenotype-commons/annotations/OMIM/by-disease/MIM-600121.tab (rev 0) +++ phenotype-commons/annotations/OMIM/by-disease/MIM-600121.tab 2009-10-20 22:10:19 UTC (rev 2863) @@ -0,0 +1,7 @@ +Disease ID Disease Name Gene ID Gene Name Genotype Gene Symbol(s) Phenotype ID Phenotype Name Entity ID Entity Name Quality ID Quality Name Add'l Entity ID Add 'l Entity Name Mode of inheritance ID Mode of inheritance Name Age of Onset ID Age of Onset Name Frequency Abnormal ID Abnormal Name Description Orthologs Pub Date Created +MIM:600121 MIM:603051 AGPS HP:0000007 +MIM:600121 MIM:603051 AGPS HP:0001508 +MIM:600121 MIM:603051 AGPS HP:0001939 GO:0008152 PATO:0000001 PATO:0000460 +MIM:600121 MIM:603051 AGPS HP:0002658 FMA:24012 PATO:0001512 +MIM:600121 MIM:603051 AGPS HP:0002968 +MIM:600121 MIM:603051 AGPS HP:0008873 Added: phenotype-commons/annotations/OMIM/by-disease/MIM-600132.tab =================================================================== --- phenotype-commons/annotations/OMIM/by-disease/MIM-600132.tab (rev 0) +++ phenotype-commons/annotations/OMIM/by-disease/MIM-600132.tab 2009-10-20 22:10:19 UTC (rev 2863) @@ -0,0 +1,3 @@ +Disease ID Disease Name Gene ID Gene Name Genotype Gene Symbol(s) Phenotype ID Phenotype Name Entity ID Entity Name Quality ID Quality Name Add'l Entity ID Add 'l Entity Name Mode of inheritance ID Mode of inheritance Name Age of Onset ID Age of Onset Name Frequency Abnormal ID Abnormal Name Description Orthologs Pub Date Created +MIM:600132 MIM:602280 TULP1 HP:0000007 +MIM:600132 MIM:602280 TULP1 HP:0000510 Added: phenotype-commons/annotations/OMIM/by-disease/MIM-600138.tab =================================================================== --- phenotype-commons/annotations/OMIM/by-disease/MIM-600138.tab (rev 0) +++ phenotype-commons/annotations/OMIM/by-disease/MIM-600138.tab 2009-10-20 22:10:19 UTC (rev 2863) @@ -0,0 +1,3 @@ +Disease ID Disease Name Gene ID Gene Name Genotype Gene Symbol(s) Phenotype ID Phenotype Name Entity ID Entity Name Quality ID Quality Name Add'l Entity ID Add 'l Entity Name Mode of inheritance ID Mode of inheritance Name Age of Onset ID Age of Onset Name Frequency Abnormal ID Abnormal Name Description Orthologs Pub Date Created +MIM:600138 MIM:606419 PRPF31 HP:0000006 +MIM:600138 MIM:606419 PRPF31 HP:0000510 Added: phenotype-commons/annotations/OMIM/by-disease/MIM-600143.tab =================================================================== --- phenotype-commons/annotations/OMIM/by-disease/MIM-600143.tab (rev 0) +++ phenotype-commons/annotations/OMIM/by-disease/MIM-600143.tab 2009-10-20 22:10:19 UTC (rev 2863) @@ -0,0 +1,13 @@ +Disease ID Disease Name Gene ID Gene Name Genotype Gene Symbol(s) Phenotype ID Phenotype Name Entity ID Entity Name Quality ID Quality Name Add'l Entity ID Add 'l Entity Name Mode of inheritance ID Mode of inheritance Name Age of Onset ID Age of Onset Name Frequency Abnormal ID Abnormal Name Description Orthologs Pub Date Created +MIM:600143 MIM:607837 CLN8 HP:0000007 +MIM:600143 MIM:607837 CLN8 HP:0000529 +MIM:600143 MIM:607837 CLN8 HP:0001250 +MIM:600143 MIM:607837 CLN8 HP:0001251 GO:0050881 PATO:0000770 +MIM:600143 MIM:607837 CLN8 HP:0001272 +MIM:600143 MIM:607837 CLN8 HP:0001336 +MIM:600143 MIM:607837 CLN8 HP:0002059 +MIM:600143 MIM:607837 CLN8 HP:0002074 +MIM:600143 MIM:607837 CLN8 HP:0002353 +MIM:600143 MIM:607837 CLN8 HP:0002376 +MIM:600143 MIM:607837 CLN8 HP:0002399 +MIM:600143 MIM:607837 CLN8 HP:0003205 Added: phenotype-commons/annotations/OMIM/by-disease/MIM-600145.tab =================================================================== --- phenotype-commons/annotations/OMIM/by-disease/MIM-600145.tab (rev 0) +++ phenotype-commons/annotations/OMIM/by-disease/MIM-600145.tab 2009-10-20 22:10:19 UTC (rev 2863) @@ -0,0 +1,12 @@ +Disease ID Disease Name Gene ID Gene Name Genotype Gene Symbol(s) Phenotype ID Phenotype Name Entity ID Entity Name Quality ID Quality Name Add'l Entity ID Add 'l Entity Name Mode of inheritance ID Mode of inheritance Name Age of Onset ID Age of Onset Name Frequency Abnormal ID Abnormal Name Description Orthologs Pub Date Created +MIM:600145 MIM:610132 VANGL1 HP:0000006 +MIM:600145 MIM:610132 VANGL1 HP:0000011 +MIM:600145 MIM:610132 VANGL1 HP:0000016 +MIM:600145 MIM:610132 VANGL1 HP:0001012 +MIM:600145 MIM:610132 VANGL1 HP:0001287 +MIM:600145 MIM:610132 VANGL1 HP:0002241 GO:0030421 PATO:0000381 +MIM:600145 MIM:610132 VANGL1 HP:0002315 +MIM:600145 MIM:610132 VANGL1 HP:0002435 +MIM:600145 MIM:610132 VANGL1 HP:0003418 +MIM:600145 MIM:610132 VANGL1 HP:0005224 +MIM:600145 MIM:610132 VANGL1 HP:0007293 Added: phenotype-commons/annotations/OMIM/by-disease/MIM-600155.tab =================================================================== --- phenotype-commons/annotations/OMIM/by-disease/MIM-600155.tab (rev 0) +++ phenotype-commons/annotations/OMIM/by-disease/MIM-600155.tab 2009-10-20 22:10:19 UTC (rev 2863) @@ -0,0 +1,5 @@ +Disease ID Disease Name Gene ID Gene Name Genotype Gene Symbol(s) Phenotype ID Phenotype Name Entity ID Entity Name Quality ID Quality Name Add'l Entity ID Add 'l Entity Name Mode of inheritance ID Mode of inheritance Name Age of Onset ID Age of Onset Name Frequency Abnormal ID Abnormal Name Description Orthologs Pub Date Created +MIM:600155 MIM:131244 EDNRB HP:0000007 +MIM:600155 MIM:131244 EDNRB HP:0002251 FMA:14543 PATO:0000586 FMA:5884 +MIM:600155 MIM:131244 EDNRB HP:0002251 FMA:14543 PATO:0000586 FMA:5884 +MIM:600155 MIM:131244 EDNRB HP:0003283 Added: phenotype-commons/annotations/OMIM/by-disease/MIM-600195.tab =================================================================== --- phenotype-commons/annotations/OMIM/by-disease/MIM-600195.tab (rev 0) +++ phenotype-commons/annotations/OMIM/by-disease/MIM-600195.tab 2009-10-20 22:10:19 UTC (rev 2863) @@ -0,0 +1,5 @@ +Disease ID Disease Name Gene ID Gene Name Genotype Gene Symbol(s) Phenotype ID Phenotype Name Entity ID Entity Name Quality ID Quality Name Add'l Entity ID Add 'l Entity Name Mode of inheritance ID Mode of inheritance Name Age of Onset ID Age of Onset Name Frequency Abnormal ID Abnormal Name Description Orthologs Pub Date Created +MIM:600195 MIM:600221 TEK HP:0000006 +MIM:600195 MIM:600221 TEK HP:0000153 PATO:0000001 PATO:0000460 +MIM:600195 MIM:600221 TEK HP:0001438 FMA:9577 PATO:0000001 PATO:0000460 +MIM:600195 MIM:600221 TEK HP:0001626 PATO:0000001 PATO:0000460 Added: phenotype-commons/annotations/OMIM/by-disease/MIM-600202.tab =================================================================== --- phenotype-commons/annotations/OMIM/by-disease/MIM-600202.tab (rev 0) +++ phenotype-commons/annotations/OMIM/by-disease/MIM-600202.tab 2009-10-20 22:10:19 UTC (rev 2863) @@ -0,0 +1,2 @@ +Disease ID Disease Name Gene ID Gene Name Genotype Gene Symbol(s) Phenotype ID Phenotype Name Entity ID Entity Name Quality ID Quality Name Add'l Entity ID Add 'l Entity Name Mode of inheritance ID Mode of inheritance Name Age of Onset ID Age of Onset Name Frequency Abnormal ID Abnormal Name Description Orthologs Pub Date Created +MIM:600202 MIM:609269 KIAA0319 HP:0006871 Added: phenotype-commons/annotations/OMIM/by-disease/MIM-600204.tab =================================================================== --- phenotype-commons/annotations/OMIM/by-disease/MIM-600204.tab (rev 0) +++ phenotype-commons/annotations/OMIM/by-disease/MIM-600204.tab 2009-10-20 22:10:19 UTC (rev 2863) @@ -0,0 +1,9 @@ +Disease ID Disease Name Gene ID Gene Name Genotype Gene Symbol(s) Phenotype ID Phenotype Name Entity ID Entity Name Quality ID Quality Name Add'l Entity ID Add 'l Entity Name Mode of inheritance ID Mode of inheritance Name Age of Onset ID Age of Onset Name Frequency Abnormal ID Abnormal Name Description Orthologs Pub Date Created +MIM:600204 MIM:120260 COL9A2 HP:0000006 +MIM:600204 MIM:120260 COL9A2 HP:0001155 PATO:0000001 PATO:0000460 +MIM:600204 MIM:120260 COL9A2 HP:0001425 +MIM:600204 MIM:120260 COL9A2 HP:0002515 +MIM:600204 MIM:120260 COL9A2 HP:0002656 FMA:24012 PATO:0000640 +MIM:600204 MIM:120260 COL9A2 HP:0003502 +MIM:600204 MIM:120260 COL9A2 HP:0004982 PATO:0000001 +MIM:600204 MIM:120260 COL9A2 HP:0005086 FMA:24974 HP:0002758 Added: phenotype-commons/annotations/OMIM/by-disease/MIM-600208.tab =================================================================== --- phenotype-commons/annotations/OMIM/by-disease/MIM-600208.tab (rev 0) +++ phenotype-commons/annotations/OMIM/by-disease/MIM-600208.tab 2009-10-20 22:10:19 UTC (rev 2863) @@ -0,0 +1,8 @@ +Disease ID Disease Name Gene ID Gene Name Genotype Gene Symbol(s) Phenotype ID Phenotype Name Entity ID Entity Name Quality ID Quality Name Add'l Entity ID Add 'l Entity Name Mode of inheritance ID Mode of inheritance Name Age of Onset ID Age of Onset Name Frequency Abnormal ID Abnormal Name Description Orthologs Pub Date Created +MIM:600208 MIM:160775 MYH9 HP:0000006 +MIM:600208 MIM:160775 MYH9 HP:0000079 +MIM:600208 MIM:160775 MYH9 HP:0000408 +MIM:600208 MIM:160775 MYH9 HP:0000478 PATO:0000001 PATO:0000460 +MIM:600208 MIM:160775 MYH9 HP:0000978 +MIM:600208 MIM:160775 MYH9 HP:0001873 +MIM:600208 MIM:160775 MYH9 HP:0001902 FMA:62851 PATO:0001940 Added: phenotype-commons/annotations/OMIM/by-disease/MIM-600224.tab =================================================================== --- phenotype-commons/annotations/OMIM/by-disease/MIM-600224.tab (rev 0) +++ phenotype-commons/annotations/OMIM/by-disease/MIM-600224.tab 2009-10-20 22:10:19 UTC (rev 2863) @@ -0,0 +1,20 @@ +Disease ID Disease Name Gene ID Gene Name Genotype Gene Symbol(s) Phenotype ID Phenotype Name Entity ID Entity Name Quality ID Quality Name Add'l Entity ID Add 'l Entity Name Mode of inheritance ID Mode of inheritance Name Age of Onset ID Age of Onset Name Frequency Abnormal ID Abnormal Name Description Orthologs Pub Date Created +MIM:600224 MIM:604985 SPTBN2 HP:0000006 +MIM:600224 MIM:604985 SPTBN2 HP:0000617 +MIM:600224 MIM:604985 SPTBN2 HP:0000639 +MIM:600224 MIM:604985 SPTBN2 HP:0001253 FMA:67944 HP:0001251 +MIM:600224 MIM:604985 SPTBN2 HP:0001260 +MIM:600224 MIM:604985 SPTBN2 HP:0001272 +MIM:600224 MIM:604985 SPTBN2 HP:0001347 +MIM:600224 MIM:604985 SPTBN2 HP:0002066 +MIM:600224 MIM:604985 SPTBN2 HP:0002070 FMA:7182 HP:0001251 +MIM:600224 MIM:604985 SPTBN2 HP:0002080 +MIM:600224 MIM:604985 SPTBN2 HP:0002276 FMA:7182 HP:0002311 +MIM:600224 MIM:604985 SPTBN2 HP:0002495 +MIM:600224 MIM:604985 SPTBN2 HP:0003590 +MIM:600224 MIM:604985 SPTBN2 HP:0003618 +MIM:600224 MIM:604985 SPTBN2 HP:0003621 +MIM:600224 MIM:604985 SPTBN2 HP:0003677 +MIM:600224 MIM:604985 SPTBN2 HP:0003743 +MIM:600224 MIM:604985 SPTBN2 HP:0004651 +MIM:600224 MIM:604985 SPTBN2 HP:0007275 FMA:72634 PATO:0001641 Added: phenotype-commons/annotations/OMIM/by-disease/MIM-600263.tab =================================================================== --- phenotype-commons/annotations/OMIM/by-disease/MIM-600263.tab (rev 0) +++ phenotype-commons/annotations/OMIM/by-disease/MIM-600263.tab 2009-10-20 22:10:19 UTC (rev 2863) @@ -0,0 +1,2 @@ +Disease ID Disease Name Gene ID Gene Name Genotype Gene Symbol(s) Phenotype ID Phenotype Name Entity ID Entity Name Quality ID Quality Name Add'l Entity ID Add 'l Entity Name Mode of inheritance ID Mode of inheritance Name Age of Onset ID Age of Onset Name Frequency Abnormal ID Abnormal Name Description Orthologs Pub Date Created +MIM:600263 IFNGR1, PTPRZ1 HP:0005202 Added: phenotype-commons/annotations/OMIM/by-disease/MIM-600274.tab =================================================================== --- phenotype-commons/annotations/OMIM/by-disease/MIM-600274.tab (rev 0) +++ phenotype-commons/annotations/OMIM/by-disease/MIM-600274.tab 2009-10-20 22:10:19 UTC (rev 2863) @@ -0,0 +1,20 @@ +Disease ID Disease Name Gene ID Gene Name Genotype Gene Symbol(s) Phenotype ID Phenotype Name Entity ID Entity Name Quality ID Quality Name Add'l Entity ID Add 'l Entity Name Mode of inheritance ID Mode of inheritance Name Age of Onset ID Age of Onset Name Frequency Abnormal ID Abnormal Name Description Orthologs Pub Date Created +MIM:600274 MAPT, PSEN1 HP:0000006 +MIM:600274 MAPT, PSEN1 HP:0000710 +MIM:600274 MAPT, PSEN1 HP:0000724 +MIM:600274 MAPT, PSEN1 HP:0000727 FMA:61824 HP:0000726 +MIM:600274 MAPT, PSEN1 HP:... 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