GlyCosmos Portal

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

Displaying entries **8701 - 8725** of **15957** in total

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Disease ID	Disease Name	Gene Symbol ▼	Gene ID	Organism	Source
DOID:0110274	autosomal recessive limb-girdle muscular dystrophy	HMG1 HMG2 PMT2 PMT3 PMT6	851171 851210 853113 854499 854900	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:1094	attention deficit hyperactivity disorder Aliases: ADHD attention deficit disorder hyperkinetic disorder	HMG1 HMG2 HRR25 TRS120	851171 852016 854900 855897	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:13404	uveoparotid fever Aliases: Heerfordt's syndrome	HLA-DRB1	3123	Homo sapiens (human)	Alliance of Genome Resources
DOID:12029	sympathetic ophthalmia Aliases: Sympathetic uveitis	HLA-DRB1	3123	Homo sapiens (human)	Alliance of Genome Resources
DOID:1395	schistosomiasis	HLA-DRB1	3123	Homo sapiens (human)	Alliance of Genome Resources
DOID:1024	leprosy	HLA-DRB1 IL17A LTA NOD2 SLC11A1 TLR1 TLR2 TNF	3123 3605 4049 64127 6556 7096 7097 7124	Homo sapiens (human)	Alliance of Genome Resources
DOID:0040091	autoimmune pancreatitis	HLA-DQB1	3119	Homo sapiens (human)	Alliance of Genome Resources
DOID:11165	common wart	HLA-DQB1	3119	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050012	chikungunya Aliases: Chikungunya fever	HLA-DQB1	3119	Homo sapiens (human)	Alliance of Genome Resources
DOID:12987	agranulocytosis Aliases: Granulocytopenic disorder Granulopenia granulocytopenia	HLA-DQB1	3119	Homo sapiens (human)	Alliance of Genome Resources
DOID:1019	osteomyelitis	HLA-DQB1	3119	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050840	cervical dystonia Aliases: spasmodic torticollis	HLA-DQB1	3119	Homo sapiens (human)	Alliance of Genome Resources
DOID:11829	degenerative myopia Aliases: degenerative progressive high myopia pathological myopia progressive high (degenerative) myopia progressive high myopia	HLA-DQB1 LRP2	3119 4036	Homo sapiens (human)	Alliance of Genome Resources
DOID:401	multidrug-resistant tuberculosis	HLA-DQB1 HLA-DRB1	3119 3123	Homo sapiens (human)	Alliance of Genome Resources
DOID:1340	pure red-cell aplasia Aliases: Red cell hypoplasia primary red cell aplasia pure red cell aplasia	HLA-DQB1 HLA-DRB1	3119 3123	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060532	latex allergy	HLA-DQB1 HLA-DRB1	3119 3123	Homo sapiens (human)	Alliance of Genome Resources
DOID:12148	alveolar echinococcosis Aliases: Multilocular hydatid alveolococcosis small fox tapeworm	HLA-DQB1 HLA-DRB1 TLR2	3119 3123 7097	Homo sapiens (human)	Alliance of Genome Resources
DOID:1495	cystic echinococcosis Aliases: Echinococcus granulosus infection Echinococcus granulosus infection of lung Echinococcus granulosus infection of thyroid Liver echinococcus granulosus Thyroid echinococcus granulosus echinococcus granulosus echinococcus granulosus infectious disease echinococcus granulosus infectious disease of liver echinococcus granulosus infectious disease of thyroid lung echinococcus granulosus unilocular echinococcosis unilocular hydatid disease	HLA-DQB1 HLA-DRB1 IL4 TLR2 TLR4	3119 3123 3565 7097 7099	Homo sapiens (human)	Alliance of Genome Resources
DOID:639	acute disseminated encephalomyelitis Aliases: ADEM acute disseminated encephalitis	HLA-DQB1 HLA-DRB1 HLA-DRB5 IFNG NEFL	3119 3123 3127 3458 4747	Homo sapiens (human)	Alliance of Genome Resources
DOID:13336	congenital toxoplasmosis Aliases: Toxoplasmosis - congen.	HLA-DQA1	3117	Homo sapiens (human)	Alliance of Genome Resources
DOID:11336	rhinoscleroma	HLA-DQA1 HLA-DQB1	3117 3119	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050748	marginal zone lymphoma Aliases: marginal zone B-cell lymphoma	HLA-DQA1 HLA-DQB1	3117 3119	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050168	autoimmune polyendocrine syndrome type 2 Aliases: Schmidt syndrome	HLA-DQA1 HLA-DQB1 HLA-DRB1	3117 3119 3123	Homo sapiens (human)	Alliance of Genome Resources
DOID:14040	autoimmune polyendocrine syndrome Aliases: Autoimmune polyglandular failure Lloyd's syndrome autoimmune polyendocrinopathy	HLA-DQA1 HLA-DQB1 HLA-DRB1	3117 3119 3123	Homo sapiens (human)	Alliance of Genome Resources
DOID:12859	choreatic disease Aliases: chorea hereditary chorea	HLA-DQA1 HLA-DQB1 HLA-DRB1 NKX2-1 VPS13A	23230 3117 3119 3123 7080	Homo sapiens (human)	Alliance of Genome Resources

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