GlyCosmos Portal

Source	Last Updated
Alliance of Genome Resources	July 29, 2024
DisGeNET	July 29, 2024
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **3326 - 3350** of **7942** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▲	Organism	Source
DOID:2518	orchitis Aliases: Inflammation of testis Orchititis	CYP19A1	1588	Homo sapiens (human)	DisGeNET
DOID:0080011	bone resorption disease	CYP19A1	1588	Homo sapiens (human)	DisGeNET
DOID:3603	mucinous cystadenocarcinoma Aliases: Pseudomucinous cystadenocarcinoma	CYP19A1	1588	Homo sapiens (human)	DisGeNET
DOID:11968	postmenopausal atrophic vaginitis Aliases: Senile vaginitis atrophic vaginitis	CYP19A1	1588	Homo sapiens (human)	DisGeNET DisGeNET
DOID:12554	hemolytic-uremic syndrome Aliases: haemolytic-uraemic syndrome hemolytic uremic syndrome	A4GALT ABO BAAT C1GALT1C1 CAT CD22 CLEC1B CYP21A2 DGKE G6PD GPI GRHPR IL1RL1 LIPG MASP1 MBL2 PIGA PLA2G7 SLC35G1 ST8SIA2 TM7SF2	1589 159371 2539 28 2821 29071 4153 51266 5277 53947 5648 570 7108 7941 8128 847 8526 9173 933 9380 9388	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:9182	pemphigus	ACE CAT CD1D CYP21A2 FCN2 MBL2 MRC1	1589 1636 2220 4153 4360 847 912	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:0060851	pemphigus vulgaris Aliases: familial pemphigus vulgaris	ACE CYP21A2 FCN2 MBL2 MRC1	1589 1636 2220 4153 4360	Homo sapiens (human)	DisGeNET DisGeNET
DOID:0060025	immunoglobulin alpha deficiency Aliases: IgA deficiency gamma-A-globulin deficiency	AGA CLEC16A CYP21A2 FUT2 FUT3 MBL2 PTEN SDC1	1589 175 23274 2524 2525 4153 5728 6382	Homo sapiens (human)	DisGeNET DisGeNET
DOID:11701	selective IgA deficiency disease Aliases: Immunoglobulin A deficiency Selective immunoglobulin A deficiency selective IgA immunodeficiency	AGA CLEC16A CYP21A2 FUT2 FUT3 MBL2 PTEN SDC1	1589 175 23274 2524 2525 4153 5728 6382	Homo sapiens (human)	DisGeNET DisGeNET
DOID:9663	aphthous stomatitis Aliases: Aphtha Aphthous ulceration Canker sore Oral aphthae oral ulcer	CAT CYP21A2 ENO1 GTDC1 LGALS1 LYZ SLC37A4 VCAM1	1589 2023 2542 3956 4069 7412 79712 847	Homo sapiens (human)	DisGeNET DisGeNET
DOID:9271	ornithine carbamoyltransferase deficiency Aliases: deficiency of citrulline phosphorylase ornithine transcarbamylase deficiency	CYP21A2 GLUL	1589 2752	Homo sapiens (human)	DisGeNET
DOID:0111416	trichohepatoenteric syndrome 2 Aliases: THES2	CYP21A2	1589	Homo sapiens (human)	DisGeNET
DOID:14757	Ehlers-Danlos syndrome hypermobility type Aliases: Ehlers-Danlos syndrome, type 3 type III Ehlers-Danlos syndrome	CYP21A2	1589	Homo sapiens (human)	DisGeNET
DOID:0050445	X-linked dominant hypophosphatemic rickets Aliases: Hypophosphatemia, Vitamin D-Resistant Rickets Vitamin D-Resistant Rickets, X-Linked X-linked hypophosphatemia hypophosphatemic rickets X-linked dominant	CYP24A1 CYP27B1 ENPP1 KL L1CAM SFTPA1 SLC2A2	1591 1594 3897 5167 6514 653509 9365	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET
DOID:1752	ocular melanoma Aliases: eye melanoma intraocular melanoma melanoma of eye	ASAH1 CD177 CYP24A1 CYP27B1 PNPLA2 SDHD	1591 1594 427 57104 57126 6392	Homo sapiens (human)	DisGeNET
DOID:10983	Alport syndrome Aliases: Hereditary Nephritis	ACE ACSL4 B3GAT1 CYP24A1	1591 1636 2182 27087	Homo sapiens (human)	DisGeNET DisGeNET
DOID:2347	generalized atherosclerosis Aliases: Generalised atherosclerosis	ABO ACE ACSM3 ARSA ATP6V0A2 CYP24A1 DGAT2 GPX3 HPGDS OLR1 PLA2G7 RENBP SELE	1591 1636 23545 27306 28 2878 410 4973 5973 6296 6401 7941 84649	Homo sapiens (human)	DisGeNET
DOID:0060700	familial hypocalciuric hypercalcemia 1 Aliases: FHH type 1 HHC1 familial benign hypercalcemia 1 familial hypocalciuric hypercalcemia type I hypocalciuric hypercalcemia type I	ALPP ATRNL1 CYP24A1 PTGS2	1591 250 26033 5743	Homo sapiens (human)	DisGeNET DisGeNET
DOID:3149	keratoacanthoma	B3GAT1 CAT CD44 CYP24A1 HK2 INPP5A MMUT MOGS MRC1 PIK3CA PLD2 PPT1 PTGS1 PTGS2 SDC1 SDHD	1591 27087 3099 3632 4360 4594 5290 5338 5538 5742 5743 6382 6392 7841 847 960	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET
DOID:0050860	colorectal adenoma	CYP24A1 GPX2 GPX3 PTGIS	1591 2877 2878 5740	Homo sapiens (human)	Alliance of Genome Resources
DOID:6945	inverted follicular keratosis Aliases: Inverted folicular keratosis	CYP24A1 HK2 INPP5A LGALS3 MMUT NTHL1 PIK3CA PIK3CB PIK3CD PIK3CG PLD2 PPT1 PTGS2 SDHD	1591 3099 3632 3958 4594 4913 5290 5291 5293 5294 5338 5538 5743 6392	Homo sapiens (human)	DisGeNET DisGeNET
DOID:11684	melanoacanthoma	CYP24A1 HK2 INPP5A LGALS3 MMUT NTHL1 PIK3CA PIK3CB PIK3CD PIK3CG PLD2 PPT1 PTGS2 SDHD	1591 3099 3632 3958 4594 4913 5290 5291 5293 5294 5338 5538 5743 6392	Homo sapiens (human)	DisGeNET DisGeNET
DOID:13197	nodular goiter Aliases: Goiter, nodular nodular goitre	ALG1 CYP24A1 LGALS3 MINPP1 TPI1	1591 3958 56052 7167 9562	Homo sapiens (human)	DisGeNET DisGeNET
DOID:1602	lymphadenitis Aliases: Adenitis Inflammation of lymph node acute adenitis acute lymphadenitis chronic Lymphadenitis chronic adenitis	CYP24A1 NTM PTEN	1591 50863 5728	Homo sapiens (human)	DisGeNET
DOID:355	mast-cell sarcoma	CAT CYP24A1	1591 847	Homo sapiens (human)	DisGeNET

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