GlyCosmos Portal

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Displaying entries **6701 - 6725** of **7942** in total

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Disease ID	Disease Name	Gene Symbol ▼	Gene ID	Organism
DOID:0060298	complement component 4b deficiency	ACE CALR CD55 FCN3 MASP2	10747 1604 1636 811 8547	Homo sapiens (human)
DOID:0060299	complement component 6 deficiency	ACE CALR CD55 FCN3 MASP2	10747 1604 1636 811 8547	Homo sapiens (human)
DOID:0060300	complement component 7 deficiency	ACE CALR CD55 FCN3 MASP2	10747 1604 1636 811 8547	Homo sapiens (human)
DOID:0060303	complement component 9 deficiency	ACE CALR CD55 FCN3 MASP2	10747 1604 1636 811 8547	Homo sapiens (human)
DOID:0060301	type I complement component 8 deficiency	ACE CALR CD55 FCN3 MASP2	10747 1604 1636 811 8547	Homo sapiens (human)
DOID:0060297	complement component 4a deficiency	ACE CALR CD55 FCN3 MASP2	10747 1604 1636 811 8547	Homo sapiens (human)
DOID:0060302	type II complement component 8 deficiency	ACE CALR CD55 FCN3 MASP2	10747 1604 1636 811 8547	Homo sapiens (human)
DOID:4449	macular retinal edema Aliases: macular edema macular oedema macular retinal oedema	ACE CALR CAT	1636 811 847	Homo sapiens (human)
DOID:4447	cystoid macular edema	ACE CALR CAT	1636 811 847	Homo sapiens (human)
DOID:13003	vertebrobasilar insufficiency Aliases: Vertebro-basilar insufficiency Vertebrobasilar arterial insufficiency Vertebrobasilar artery syndrome	ACE CALR CAT CD74 CHKA CYP2C19 DHCR24 FCN1 G6PD GLA GPX3 ICAM1 LTC4S MCFD2 NAMPT OGG1 OLR1 PARP1 PIGA PIK3CA PIK3CB PIK3CD PIK3CG PLA2G7 PTEN PTGS2 SELL SELP SIRT6 SMPD3 SULT1E1	10135 1119 142 1557 1636 1718 2219 2539 2717 2878 3383 4056 4968 4973 51548 5277 5290 5291 5293 5294 55512 5728 5743 6402 6403 6783 7941 811 847 90411 972	Homo sapiens (human)
DOID:626	complement deficiency Aliases: Complement deficiency disease	ACE CALR CAT CD14 CD55 CEL CHI3L1 CHIT1 CYP21A2 CYP27B1 EPHX2 FCGR3B FCN3 IL18R1 LGALS1 LYZ MANBA MASP2 MRC1 NCAM1 PARP9 PIK3CA PIK3CB PIK3CD PIK3CG PLB1 PTGS2 RECK SELE SLC27A5 SMUG1 SOAT1 ST8SIA4 VTCN1	1056 10747 10998 1116 1118 151056 1589 1594 1604 1636 2053 2215 23583 3956 4069 4126 4360 4684 5290 5291 5293 5294 5743 6401 6646 7903 79679 811 83666 8434 847 8547 8809 929	Homo sapiens (human)
DOID:11335	sarcoidosis Aliases: Boeck sarcoid lymphogranulomatosis	ACE CALR CAT CD14 CD55 CEL CHI3L1 CHIT1 CYP21A2 CYP27B1 EPHX2 FCGR3B FCN3 IL18R1 LGALS1 LYZ MANBA MASP2 MRC1 NCAM1 PARP9 PIK3CA PIK3CB PIK3CD PIK3CG PLB1 PTGS2 RECK SELE SFTPD SLC27A5 SMUG1 SOAT1 ST8SIA4 VTCN1	1056 10747 10998 1116 1118 151056 1589 1594 1604 1636 2053 2215 23583 3956 4069 4126 4360 4684 5290 5291 5293 5294 5743 6401 6441 6646 7903 79679 811 83666 8434 847 8547 8809 929	Homo sapiens (human)
DOID:10845	St. Louis encephalitis Aliases: Neuroinvasive St. Louis encephalitis virus infection	ACE CALR CAT CD14 CD33 CD48 FCN2 GLT1D1 LGALS1 MICA PIK3CD SELL SELP SEMA7A SGMS1 SIGLEC1 SOAT1	100507436 144423 1636 2220 259230 3956 5293 6402 6403 6614 6646 811 847 8482 929 945 962	Homo sapiens (human)
DOID:10930	borderline personality disorder	ACE CACNA2D4 COMT DBT DGKH ETNPPL FADS1 G6PD GAD1 GAD2 GPC1 IMPA2 LDHA LMAN2L MCAT MPPE1 PLCG1 SYNJ1	1312 160851 1629 1636 2539 2571 2572 27349 2817 3613 3939 3992 5335 64850 65258 81562 8867 93589	Homo sapiens (human)
DOID:10808	gastric ulcer Aliases: acute gastric ulcer with haemorrhage and perforation acute gastric ulcer with hemorrhage AND with perforation but without obstruction acute gastric ulcer with hemorrhage and obstruction acute gastric ulcer with hemorrhage and perforation acute gastric ulcer with hemorrhage and perforation, with obstruction acute gastric ulcer with hemorrhage and perforation, without mention of obstruction acute gastric ulcer with hemorrhage, with obstruction acute gastric ulcer with hemorrhage, with perforation AND with obstruction acute gastric ulcer with perforation acute gastric ulcer with perforation AND obstruction acute gastric ulcer with perforation, with obstruction acute gastric ulcer without hemorrhage and without perforation acute gastric ulcer without hemorrhage, without perforation AND without obstruction acute gastric ulcer without mention of hemorrhage or perforation, without mention of obstruction bleeding acute gastric ulcer chronic gastric ulcer without hemorrhage AND without perforation chronic gastric ulcer without hemorrhage AND without perforation but with obstruction chronic gastric ulcer without mention of hemorrhage or perforation, with obstruction	ACE BAD CAT CYP2C19 CYP2C9 EFNA5 FUT4 GPX1 IDUA LGALS1 MGLL PLA2G4A PTGS1 PTGS2 TFF1	11343 1557 1559 1636 1946 2526 2876 3425 3956 5321 572 5742 5743 7031 847	Homo sapiens (human)
DOID:11123	Henoch-Schoenlein purpura Aliases: Allergic purpura Autoimmune purpura Henoch-Sch?nlein purpura Henoch-Sch@nlein purpura Henoch-Scholein purpura Henoch-Schonlein Purpura Purpura, autoimmune	ACE B4GALNT1 C1GALT1 CPT1C CYP19A1 CYP2U1 CYP7B1 GBA2 ICAM1 L1CAM MBL2 MGAT5 NAAA PARP1 PLA2G6 PLD3 PNPLA6 SLC33A1	10908 113612 126129 142 1588 1636 23646 2583 27163 3383 3897 4153 4249 56913 57704 8398 9197 9420	Homo sapiens (human)
DOID:11111	hydronephrosis	ACE B3GLCT B4GAT1 CHST14 COG1 COG7 CPT2 CYP1A1 EBP G6PC3 GPC3 HPSE2 IDH2 MASP1 NAGLU NSDHL OGA PGAP2 PGAP3 PIGL PIGN PIGO PIGQ PIGV PIGW PIGY PLD1 PTGES PTGS2 TBXAS1 VNN1	10682 10724 11041 113189 1376 145173 1543 1636 23556 2719 27315 284098 3418 4669 50814 5337 55650 5648 5743 60495 6916 84720 84992 8876 9091 91949 92579 93210 9382 9487 9536	Homo sapiens (human)
DOID:0080491	cerebral cavernous malformation 1	ACE B3GAT1 CEACAM5 CHI3L1 CYP2B6 GLO1 ICAM1 NCAM1 PTEN PTGIS PTGS2 STS	1048 1116 1555 1636 27087 2739 3383 412 4684 5728 5740 5743	Homo sapiens (human)
DOID:854	collagen disease Aliases: collagen disorder	ACE B3GALT6 B4GALT7 CD22 COL9A2 CYP3A5 DCN GLB1 HPRT1 NT5E PCYT1A PKD1 PKD2 PLOD3 SCP2 SELE SLC2A10 TLR4	11285 126792 1298 1577 1634 1636 2720 3251 4907 5130 5310 5311 6342 6401 7099 81031 8985 933	Homo sapiens (human)
DOID:9675	pulmonary emphysema	ACE ATP6V0A2 CAT CD74 CEACAM5 CEACAM7 CH25H CHI3L1 CYP2B6 EPHX2 FDPS FUT8 GCLC GPX1 IL18R1 ISYNA1 KL LGALS9 LMAN2L MAN1C1 PARP1 PIK3CA PTEN PTGS2 RGN SFTPC SFTPD SGMS2 SIGLEC9 SLC2A10 SMPD2 SMPD3 SOAT1 TLR4 TM7SF2 VCAN	1048 1087 1116 142 1462 1555 1636 166929 2053 2224 23545 2530 27180 2729 2876 3965 51477 5290 55512 57134 5728 5743 6440 6441 6610 6646 7099 7108 81031 81562 847 8809 9023 9104 9365 972	Homo sapiens (human)
DOID:0080205	CAKUT Aliases: Congenital anomalies of the kidney and urinary tract Renal or urinary tract malformation	ACE ATP6AP2 FREM1 PIK3CA PIK3CB PIK3CD PIK3CG	10159 158326 1636 5290 5291 5293 5294	Homo sapiens (human)
DOID:841	extrinsic allergic alveolitis Aliases: alveolitis hypersensitivity pneumonitis	ACE ATP6AP2 CEL CHI3L1 CYP2E1 LGALS9 PARP9 SFTPA1 SLC27A5 TNF	10159 1056 10998 1116 1571 1636 3965 653509 7124 83666	Homo sapiens (human)
DOID:4028	angioma serpiginosum Aliases: Angioma serpiginosum of skin	ACE ATP6AP2 ATP6V1A C1GALT1C1 MAG PIK3CA PIK3CB PIK3CD PIK3CG PTEN SRD5A3	10159 1636 29071 4099 523 5290 5291 5293 5294 5728 79644	Homo sapiens (human)
DOID:2725	capillary hemangioma Aliases: Capillary haemangioma Congenital vascular hamartoma Congenital vascular naevus Infantile hemangioma Juvenile hemangioma Strawberry haemangioma Strawberry nevus Strawberry nevus of skin cellular hemangioma of Infancy	ACE ATP6AP2 ATP6V1A C1GALT1C1 CYP1B1 GNPTAB MAG MTM1 MTMR14 PIK3CA PIK3CB PIK3CD PIK3CG PTEN SDHC SDHD SRD5A3	10159 1545 1636 29071 4099 4534 523 5290 5291 5293 5294 5728 6391 6392 64419 79158 79644	Homo sapiens (human)
DOID:483	cavernous hemangioma Aliases: Cavernoma Cavernous haemangioma	ACE ATP6AP2 ATP6V1A C1GALT1C1 CALR CD14 CTSA CYP1B1 DPM1 GAS1 GNPTAB GPC6 HSD17B2 IDH1 IDH2 IGF2R IL18R1 MAG MTM1 MTMR14 PIGF PIK3CA PIK3CB PIK3CD PIK3CG PKD1 PNPLA2 PNPLA6 PTEN SDHC SDHD SRD5A3	10082 10159 10908 1545 1636 2619 29071 3294 3417 3418 3482 4099 4534 523 5281 5290 5291 5293 5294 5310 5476 57104 5728 6391 6392 64419 79158 79644 811 8809 8813 929	Homo sapiens (human)

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