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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 **4301 - 4325** of **7942** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▼	Organism	Source
DOID:4372	intracranial embolism Aliases: Cerebral embolism with cerebral infarction cerebral embolism	Kl	16591	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:12466	secondary hyperparathyroidism	Kl	16591	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:1074	kidney failure Aliases: renal failure	Kl Nampt Ppargc1a Tlr2 Tlr4	16591 19017 21898 24088 59027	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:784	chronic kidney disease Aliases: CKD CRF chronic kidney failure chronic renal disease chronic renal failure syndrome renal failure - chronic	Dgat2 Kl Lepr Rbp4	16591 16847 19662 67800	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111680	essential fructosuria Aliases: fructokinase deficiency hepatic fructokinase deficiency ketohexokinase deficiency	Khk	16548	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:10273	heart conduction disease Aliases: heart rhythm disease	Kcnq1	16535	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050793	short QT syndrome	Kcnq1	16535	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:2843	long QT syndrome Aliases: LQT long Q-T syndrome	Kcnq1	16535	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050650	familial atrial fibrillation Aliases: ATFB	Kcnq1	16535	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110644	long QT syndrome 1 Aliases: LQT1 ventricular fibrillation with prolonged QT interval	Kcnq1	16535	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:5572	Beckwith-Wiedemann syndrome	Kcnq1	16535	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:2842	Jervell-Lange Nielsen syndrome Aliases: Jervell and Lange-Nielson syndrome	Kcnq1	16535	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0060224	atrial fibrillation Aliases: A-fib AFib	Kcnq1 Tlr2 Tnf	16535 21926 24088	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:4440	seminoma Aliases: Seminoma, Pure	Kcnq1 Pcna Tymp	16535 18538 72962	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0070218	familial hyperinsulinemic hypoglycemia 2 Aliases: Autosomal recessive hyperinsulinemic hypoglycemia due to Kir6.2 deficiency HHF2 hyperinsulinemic hypoglycemia due to focal adenomatous hyperplasia	Kcnj11	16514	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111110	maturity-onset diabetes of the young type 13 Aliases: MODY type 13 MODY13	Kcnj11	16514	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080569	congenital disorder of glycosylation Ir Aliases: congenital disorder of glycosylation 1r	DDOST	1650	Homo sapiens (human)	Glyco-Disease Genes Database DisGeNET Alliance of Genome Resources
DOID:600	animal phobia Aliases: Fear of animals Zoophobia	CAT DDOST	1650 847	Homo sapiens (human)	DisGeNET DisGeNET
DOID:599	specific phobia Aliases: simple phobia	CAT DDOST	1650 847	Homo sapiens (human)	DisGeNET DisGeNET
DOID:10112	sleeping sickness Aliases: African sleeping sickness African trypanosomiasis	ACHE DDOST GAPDH MTAP PIGB SMUG1 STT3A STT3B	1650 201595 23583 2597 3703 43 4507 9488	Homo sapiens (human)	DisGeNET DisGeNET Alliance of Genome Resources
DOID:0110061	amelogenesis imperfecta hypomaturation type 2A3 Aliases: AI2A3 amelogenesis imperfecta hypomaturation type IIA3 amelogenesis imperfecta type IIA3	AKR1C1 AKR1C2 MMP25 TMEM165	1645 1646 55858 64386	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET
DOID:0110057	amelogenesis imperfecta type 2A1 Aliases: AI2A1 amelogenesis imperfecta pigmented hypomaturation type 1 amelogenesis imperfecta type IIA1	AKR1C1 AKR1C2 MMP25 TMEM165	1645 1646 55858 64386	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET
DOID:0110059	X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2 Aliases: AIH3 amelogenesis imperfecta type IE X-linked 2 amelogenesis imperfecta 3 hypoplastic type	AKR1C1 AKR1C2 MMP25 TMEM165	1645 1646 55858 64386	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET
DOID:0110065	amelogenesis imperfecta type 1F Aliases: AI1F amelogenesis imperfecta hypoplastic type IF amelogenesis imperfecta type IF	AKR1C1 AKR1C2 MMP25 TMEM165	1645 1646 55858 64386	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET
DOID:0110063	amelogenesis imperfecta hypomaturation type 2A5 Aliases: AI2A5 amelogenesis imperfecta hypomaturation type IIA5 amelogenesis imperfecta type IIA5	AKR1C1 AKR1C2 MMP25 TMEM165	1645 1646 55858 64386	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET

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