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GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB), DisGeNET, and Alliance of Genome Resources is integrated into one list.

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

Displaying entries **2751 - 2775** of **4621** in total

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Disease ID	Disease Name	Gene Symbol ▲	Gene ID	Organism
DOID:4830	adenosquamous carcinoma Aliases: Adenosquamous cell carcinoma mixed adenocarcinoma and squamous carcinoma	CALR CLEC10A MGLL PGK1 PIK3CA PTEN SIGLEC7	10462 11343 27036 5230 5290 5728 811	Homo sapiens (human)
DOID:1729	retinal vascular occlusion Aliases: Retinal vasc. occlusion	CALR CNTN2 PIK3CA	5290 6900 811	Homo sapiens (human)
DOID:8955	sideroblastic anemia Aliases: ANEMIA SIDEROBLASTIC Anemia, hypochromic with iron loading	CALR CYP2E1	1571 811	Homo sapiens (human)
DOID:8649	tongue cancer Aliases: malignant neoplasm of tongue	CALR DAG1 GOLPH3 HPSE KLRC1 LGALS3 LSS NANS PIK3CA PIK3CB PIK3CD PIK3CG PLAUR PTEN PTGS2	10855 1605 3821 3958 4047 5290 5291 5293 5294 5329 54187 5728 5743 64083 811	Homo sapiens (human)
DOID:0060777	congenital secretory sodium diarrhea 8 Aliases: DIAR8	CALR DGAT1 PTGS2	5743 811 8694	Homo sapiens (human)
DOID:0060781	congenital secretory sodium diarrhea 3 Aliases: congenital secretory sodium diarrhea 3 syndromic congenital secretory sodium diarrhea 3 with or without other congenital anomalies congenital secretory sodium diarrhoea 3 congenital secretory sodium diarrhoea 3 syndromic congenital secretory sodium diarrhoea 3 with or without other congenital anomalies	CALR DGAT1 PTGS2	5743 811 8694	Homo sapiens (human)
DOID:0080531	dedifferentiated liposarcoma	CALR ENPP2 FASN KL PARP1 PIK3CA PIK3CB PIK3CD PIK3CG PSMD10 PTEN SDC1 STS	142 2194 412 5168 5290 5291 5293 5294 5716 5728 6382 811 9365	Homo sapiens (human)
DOID:0050731	vitamin B12 deficiency Aliases: cobalamin deficiency hypocobalaminemia	CALR FUT2 GPX3	2524 2878 811	Homo sapiens (human)
DOID:5339	cyclic hematopoiesis Aliases: Cyclic neutropenia Cyclical neutropenia Neutropenia, periodic cyclic agranulocytosis	CALR G6PC3 IL1R1 PNP PRKAA2 PTGS2 SLC35A2	3554 4860 5563 5743 7355 811 92579	Homo sapiens (human)
DOID:7427	anthrax disease	CALR GALNS HACD1 LGALS1 PARP1 PLB1 STT3A	142 151056 2588 3703 3956 811 9200	Homo sapiens (human)
DOID:11678	onchocerciasis Aliases: Infection by Onchocerca volvulus Onchocerca volvulus infection volvulosis	CALR HPGDS	27306 811	Homo sapiens (human)
DOID:7166	thyroiditis	CALR ICAM1 PIK3CA PIK3CB PIK3CD PIK3CG PTEN SELL	3383 5290 5291 5293 5294 5728 6402 811	Homo sapiens (human)
DOID:3342	bone inflammation disease Aliases: Inflammatory disorder of bone bone inflammatory disease osteitis	CALR MBL2	4153 811	Homo sapiens (human)
DOID:10301	parotitis	CALR PIK3CD	5293 811	Homo sapiens (human)
DOID:10303	sialadenitis Aliases: Sialoadenitis	CALR PIK3CD	5293 811	Homo sapiens (human)
DOID:11258	cat-scratch disease Aliases: Debre's Syndrome Debre-Mollaret Syndrome Foshay-Mollaret Cat Scratch Fever benign lymphoreticulosis cat scratch fever	CALR PTGS2 SMUG1	23583 5743 811	Homo sapiens (human)
DOID:13800	inclusion conjunctivitis Aliases: Chlamydial conjunctivitis Inclusion blennorrhoea adult inclusion conjunctivitis inclusion blenorrhea	CALR PTGS2 SMUG1	23583 5743 811	Homo sapiens (human)
DOID:990	congenital heart block	CALR SIGLEC1	6614 811	Homo sapiens (human)
DOID:13405	cardiac sarcoidosis	CALR SMUG1	23583 811	Homo sapiens (human)
DOID:0111146	acquired von Willebrand syndrome Aliases: AVWS	CALR	811	Homo sapiens (human)
DOID:7428	pineal region germinoma	CALR	811	Homo sapiens (human)
DOID:0050800	cerebral creatine deficiency syndrome 1 Aliases: CEREBRAL CREATINE DEFICIENCY SYNDROME 1 SLC6A8 deficiency creatine transporter deficiency	CALR	811	Homo sapiens (human)
DOID:10022	ampulla of Vater benign neoplasm Aliases: tumor of the ampulla of Vater	CALR	811	Homo sapiens (human)
DOID:7442	monoclonal gammopathy of uncertain significance Aliases: MGUS Monoclonal gammopathy of undetermined significance	CANX CD38 CLEC12A COLEC10 ENPP1 FUT4 GPNMB HAS1 KL KLRK1 LPL MAG NCAM1 PARP1 PNP PRSS21 SDC1 TNKS	10457 10584 10942 142 160364 22914 2526 3036 4023 4099 4684 4860 5167 6382 821 8658 9365 952	Homo sapiens (human)
DOID:9669	senile cataract	CAT CD14 EFNA5 G6PD GALK1 GPX1 HPGDS LSS OGG1 PARP1 PLCD3	113026 142 1946 2539 2584 27306 2876 4047 4968 847 929	Homo sapiens (human)

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