GlyCosmos Portal

Table Filtering

Disease ID

Disease Name

Gene Symbol

Gene ID

Organism

Source

Display
results per page.

Clear

Submissions

GlyCosmos Diseases

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

Source	Last Updated
Alliance of Genome Resources	October 9, 2024
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **1501 - 1525** of **4649** in total

« First

‹ Prev

…

57

58

59

60

61

62

63

64

65

…

Next ›

Last »
Disease ID	Disease Name	Gene Symbol	Gene ID ▲	Organism	Source
DOID:12466	secondary hyperparathyroidism	ABCG2 CASR ENG KL PTGS2 TNFRSF11B	2022 4982 5743 846 9365 9429	Homo sapiens (human)	Alliance of Genome Resources
DOID:12783	migraine without aura Aliases: common migraine	ENO2 LDLR TNF	2026 3949 7124	Homo sapiens (human)	Alliance of Genome Resources
DOID:1800	neuroendocrine carcinoma	ENO2	2026	Homo sapiens (human)	Alliance of Genome Resources
DOID:0112242	congenital symmetric circumferential skin creases 1 Aliases: CSCSC1	TUBB	203068	Homo sapiens (human)	Alliance of Genome Resources
DOID:0090136	complex cortical dysplasia with other brain malformations 6 Aliases: CDCBM56	TUBB	203068	Homo sapiens (human)	Alliance of Genome Resources
DOID:6652	diffuse idiopathic skeletal hyperostosis Aliases: Ankylosing vertebral hyperostosis DISH Disseminated idiopathic skeletal hyperostosis	SLC29A1	2030	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060213	frontotemporal dementia and/or amyotrophic lateral sclerosis 1 Aliases: ALSFTD FTDALS1 FTDMND amyotrophic lateral sclerosis and/or frontotemporal dementia frontotemporal dementia and/or motor neuron disease	C9orf72	203228	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060319	cardiac arrest Aliases: cardiopulmonary arrest circulatory arrest	ABCC8 CCL5 EP300 ITPR1 TNF TRPM4	2033 3708 54795 6352 6833 7124	Homo sapiens (human)	Alliance of Genome Resources
DOID:3669	intermittent claudication Aliases: Charcot's syndrome	BAD BAX EPAS1 MDM2 SIRT2	2034 22933 4193 572 581	Homo sapiens (human)	Alliance of Genome Resources
DOID:12716	newborn respiratory distress syndrome Aliases: HMD - Hyaline membrane disease Neonatal respiratory Distress syndrome hyaline membrane disease pulmonary hyaline membrane disease pulmonary hypoperfusion syndrome of newborn respiratory distress syndrome of newborn	CAT EPAS1 ICAM1 MBL2 NDST1 NPSR1 SFTPA1 SFTPA2 SFTPB SFTPC SFTPD SOD1 VEGFA	2034 3340 3383 387129 4153 6439 6440 6441 653509 6647 729238 7422 847	Homo sapiens (human)	Alliance of Genome Resources
DOID:14175	von Hippel-Lindau disease Aliases: Hippel Lindau syndrome von Hippel-Lindau syndrome	EPAS1 MMP3 SLC18A1	2034 4314 6570	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080339	familial erythrocytosis 4 Aliases: ECYT4	EPAS1	2034	Homo sapiens (human)	Alliance of Genome Resources
DOID:2373	hereditary elliptocytosis Aliases: Congenital elliptocytosis ovalocytosis	EPB41 SLC4A1	2035 6521	Homo sapiens (human)	Alliance of Genome Resources
DOID:0070041	autosomal dominant intellectual developmental disorder 11 Aliases: MRD11 autosomal dominant mental retardation 11 autosomal dominant non-syndromic intellectual disability 11	EPB41L1	2036	Homo sapiens (human)	Alliance of Genome Resources
DOID:12971	hereditary spherocytosis Aliases: Congenital spherocytic hemolytic anemia Minkowski Chauffard syndrome spherocytic anemia	ANK1 EPB42 SLC4A1 SPTA1 SPTB	2038 286 6521 6708 6710	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110284	autosomal recessive limb-girdle muscular dystrophy type 2L Aliases: LGMD2L muscular dystrophy, limb-girdle, type 2L	ANO5 FKTN	203859 2218	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111533	gnathodiaphyseal dysplasia Aliases: GDD Levin syndrome 2 gnathodiaphyseal sclerosis osteogenesis imperfecta with unusual skeletal lesions osteogenesis imperfecta, Levin type	ANO5	203859	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111338	isolated elevated serum creatine phosphokinase levels Aliases: elevated serum CPK idiopathic hyperCKemia isolated hyperCKemia	ANO5	203859	Homo sapiens (human)	Alliance of Genome Resources
DOID:0070201	Miyoshi muscular dystrophy 3 Aliases: MMD3 Miyoshi myopathy 3	ANO5	203859	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110920	hereditary spherocytosis type 5 Aliases: HS5 SPH5 hereditary spherocytosis 5	EPB42	2038	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060718	autosomal recessive congenital ichthyosis 9 Aliases: ARCI9	CERS3	204219	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080685	aortic dissection	ACTA1 EFEMP2 EPHB1 NONO SPP1	2047 30008 4841 58 6696	Homo sapiens (human)	Alliance of Genome Resources
DOID:2218	blood platelet disease Aliases: Thrombocytopathy platelet disorder	CD36 EPHB2 FLI1 GP6 ITGB3 TBXA2R TPM4	2048 2313 3690 51206 6915 7171 948	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060020	reticular dysgenesis Aliases: De Vaal disease	AK2	204	Homo sapiens (human)	Alliance of Genome Resources
DOID:264	hemangiopericytoma Aliases: Haemangiopericytic meningioma hemangiopericytoma, malignant malignant hemangiopericytoma	DLL4 EPHB4 HES1 KDR NOTCH1 NOTCH4 PTEN	2050 3280 3791 4851 4855 54567 5728	Homo sapiens (human)	Alliance of Genome Resources

Download data in CSV format Download data in TSV format Download data in JSON format

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

LM-GlycoRepo

All Resources

Other Information

Tools

Search Tools

Guidelines

International Collaboration

Acknowledgements