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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	July 29, 2024
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **2976 - 3000** of **7942** in total

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Disease ID	Disease Name	Gene Symbol ▼	Gene ID	Organism
DOID:13317	hyperinsulinemic hypoglycemia Aliases: Islet cell hyperplasia nesidioblastosis persistent hyperinsulinemia hypoglycemia of infancy	Hex-t1 Hex-t2	117364 43191	Drosophila melanogaster (fruit fly)
DOID:10584	retinitis pigmentosa Aliases: pericentral pigmentary retinopathy	Hex-t1 Hex-t2	117364 43191	Drosophila melanogaster (fruit fly)
DOID:11714	gestational diabetes Aliases: GDM Gestational diabetes mellitus Maternal gestational diabetes mellitus	Hex-t1 Hex-t2 Ogg1	117364 31806 43191	Drosophila melanogaster (fruit fly)
DOID:3393	coronary artery disease Aliases: CHD Coronary disease coronary arteriosclerosis coronary heart disease	Hex-t1 Hex-t2 Idgf1 Idgf2 Idgf3 Idgf4 Idgf5 Idgf6 Ogg1 Tl	117364 31806 31926 34978 34979 34981 36868 37104 43191 43222	Drosophila melanogaster (fruit fly)
DOID:9409	diabetes insipidus	Has2	25694	Rattus norvegicus (Norway rat)
DOID:9409	diabetes insipidus	Has2	15117	Mus musculus (house mouse)
DOID:6432	pulmonary hypertension	Has1 Has2 Has3 Hk1 Hmgb1 Hyal1 Myc Nampt Pgf Tnf	24577 24835 25058 25459 25694 266805 282821 297508 367166 94203	Rattus norvegicus (Norway rat)
DOID:6432	pulmonary hypertension	Has1 Has2 Has3 Hk1 Hmgb1 Hyal1 Hyal2 Myc Nampt Pgf Tnf	15116 15117 15118 15275 15289 15586 15587 17869 18654 21926 59027	Mus musculus (house mouse)
DOID:0050809	mucopolysaccharidosis IX	HYAL1 HYAL2	3373 8692	Homo sapiens (human)
DOID:6432	pulmonary hypertension	HXK1 RHO1	850614 856294	Saccharomyces cerevisiae S288C
DOID:0110196	Charcot-Marie-Tooth disease type 4G Aliases: CMT4G Charcot-Marie-Tooth neuropathy type 4G HMSNR autosomal recessive Charcot-Marie-Tooth disease type 4G hereditary motor and sensory neuropathy Russe type	HXK1 HXK2	850614 852639	Saccharomyces cerevisiae S288C
DOID:10923	sickle cell anemia Aliases: Hb SC disease Hb-S/Hb-C disease Hb-SS disease without crisis Hemoglobin S disease without crisis Sickle-cell/Hb-C disease without crisis drepanocytosis haemoglobin SC disease hemoglobin SC disease sickle cell anaemia	HXK1 HXK2	850614 852639	Saccharomyces cerevisiae S288C
DOID:2355	anemia Aliases: anaemia	HXK1 HXK2 ZWF1	850614 852639 855480	Saccharomyces cerevisiae S288C
DOID:9952	acute lymphoblastic leukemia Aliases: ALL acute lymphoblastic leukaemia acute lymphocytic leukaemia precursor lymphoblastic lymphoma/leukemia	HXK1 HXK2 PGI1	850614 852495 852639	Saccharomyces cerevisiae S288C
DOID:2861	congenital nonspherocytic hemolytic anemia Aliases: HNSHA congenital nonspherocytic hemolytic anaemia hereditary nonspherocytic hemolytic anaemia hereditary nonspherocytic hemolytic anemia	HXK1 HXK2 PGI1 PYK2 ZWF1	850614 852495 852639 854529 855480	Saccharomyces cerevisiae S288C
DOID:252	alcoholic psychosis Aliases: Alcoholic psychoses	HTR2A	3356	Homo sapiens (human)
DOID:9159	gas gangrene Aliases: Gas bacillus infection	HSPG2	3339	Homo sapiens (human)
DOID:0050788	proximal symphalangism Aliases: Cushing's symphalangism	HSPG2 SDC2	3339 6383	Homo sapiens (human)
DOID:12144	low compliance bladder Aliases: Low bladder compliance hyperactivity of bladder hypertonic bladder hypertonicity of bladder	HSPG2 ICAM1	3339 3383	Homo sapiens (human)
DOID:0050590	severe congenital neutropenia	HSP104	850633	Saccharomyces cerevisiae S288C
DOID:0081133	3-methylglutaconic aciduria type 7a	HSP104	850633	Saccharomyces cerevisiae S288C
DOID:0081134	3-methylglutaconic aciduria type 7b	HSP104	850633	Saccharomyces cerevisiae S288C
DOID:0070224	progressive familial intrahepatic cholestasis 4 Aliases: PFIC4 TJP2 deficit	HSD3B7	80270	Homo sapiens (human)
DOID:0111071	congenital bile acid synthesis defect 1 Aliases: CBAS1	HSD3B7	80270	Homo sapiens (human)
DOID:4085	trophoblastic neoplasm Aliases: Trophoblastic tumor	HSD3B1 LGALS1	3283 3956	Homo sapiens (human)

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