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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	October 9, 2024
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **10351 - 10375** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▼	Organism	Source
DOID:2383	neonatal jaundice Aliases: neonatal hyperbilirubinemia neonatal icterus	gspd-1	178046	Caenorhabditis elegans	Alliance of Genome Resources
DOID:2861	congenital nonspherocytic hemolytic anemia Aliases: HNSHA congenital nonspherocytic hemolytic anaemia hereditary nonspherocytic hemolytic anaemia hereditary nonspherocytic hemolytic anemia	gspd-1	178046	Caenorhabditis elegans	Alliance of Genome Resources
DOID:14067	Plasmodium falciparum malaria Aliases: Malaria fever, subtertian falciparum malaria malignant tertian fever	gspd-1	178046	Caenorhabditis elegans	Alliance of Genome Resources
DOID:13628	favism	gspd-1	178046	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0112312	male infertility due to globozoospermia Aliases: globozoospermia syndrome	enpl-1	178014	Caenorhabditis elegans	Alliance of Genome Resources
DOID:2748	glycogen storage disease III Aliases: Glycogen storage disease 3 Glycogen storage disease, type III amylo 1,6 glucosidase deficiency deficiency of debranching enzyme deficiency of dextrin	AGL	178	Homo sapiens (human)	Alliance of Genome Resources
DOID:0070254	congenital disorder of glycosylation type IIb Aliases: CDG IIb CDG2B CDGIIb glucosidase I deficiency	mogs-1	177998	Caenorhabditis elegans	Alliance of Genome Resources
DOID:2590	familial nephrotic syndrome Aliases: Congenital nephrotic syndrome	epi-1	177956	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0060738	junctional epidermolysis bullosa non-Herlitz type Aliases: GABEB JEB-nH gen JEN-nH generalized atrophic benign epidermolysis bullosa generalized junctional epidermolysis bullosa, non-Herlitz type junctional epidermolysis bullosa generalisata mitis junctional epidermolysis bullosa, Disentis type	epi-1	177956	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0111583	carboxypeptidase N deficiency Aliases: anaphylotoxin inactivator deficiency deficiency of carboxypeptidase B	cpd-2 egl-21	177940 181684	Caenorhabditis elegans	Alliance of Genome Resources
DOID:11981	morbid obesity Aliases: Severe obesity	cpd-2 egl-21	177940 181684	Caenorhabditis elegans	Alliance of Genome Resources
DOID:2236	congenital afibrinogenemia Aliases: Factor I deficiency Fibrinogen deficiency	Y43C5A.2	177911	Caenorhabditis elegans	Alliance of Genome Resources
DOID:14735	hereditary angioedema Aliases: HANE Hereditary angioneurotic edema	Y43C5A.2 hst-3.2	177911 3564879	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0060903	thrombosis	W01F3.2 Y43C5A.2 acn-1 srp-1 srp-3 srp-7 zmp-3 zmp-4	177911 178585 178672 178748 179195 179991 180351 180780	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0080442	developmental and epileptic encephalopathy 41 Aliases: DEE41 early infantile epileptic encephalopathy 41	glt-1 glt-3 glt-6	177882 180641 187623	Caenorhabditis elegans	Alliance of Genome Resources
DOID:3307	teratoma	cwn-2	177870	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0060766	autosomal dominant Robinow syndrome 1 Aliases: DRS1	cwn-2	177870	Caenorhabditis elegans	Alliance of Genome Resources
DOID:1911	endodermal sinus tumor Aliases: Hepatoid yolk sac tumour Yolk Sac neoplasm Yolk sac tumour endodermal sinus tumour infantile embryonal carcinoma yolk sac tumor	cwn-2	177870	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0060254	Robinow syndrome Aliases: Robinow dwarfism acral dysostosis with facial and genital abnormalities fetal face syndrome	cwn-2	177870	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0060774	congenital diarrhea	cwn-2	177870	Caenorhabditis elegans	Alliance of Genome Resources
DOID:90	degenerative disc disease Aliases: cervical disc degenerative disease intervertebral disc degeneration lumbar disc degeneration vertebral disc disease	cri-2 gon-1 zmp-3	177850 178748 179197	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0110175	Charcot-Marie-Tooth disease axonal type 2O Aliases: Charcot-Marie-Tooth neuropathy axonal type 2O autosomal dominant Charcot-Marie-Tooth disease type 2O autosomal dominant axonal Charcot-Marie-Tooth disease type 2O	DYNC1H1	1778	Homo sapiens (human)	Alliance of Genome Resources
DOID:0070043	autosomal dominant intellectual developmental disorder 13 Aliases: MRD13 autosomal dominant mental retardation 13 autosomal dominant non-syndromic intellectual disability 13 mental retardation, autosomal dominant 13, with neuronal migration defects	DYNC1H1	1778	Homo sapiens (human)	Alliance of Genome Resources
DOID:0070351	spinal muscular atrophy with lower extremity predominant 1 Aliases: spinal muscular atrophy with lower extremity predominance 1	DYNC1H1	1778	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050429	Hailey-Hailey disease Aliases: BENIGN CHRONIC PEMPHIGUS Pemphigus, Benign Familial	mca-1	177795	Caenorhabditis elegans	Alliance of Genome Resources

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