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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 **10326 - 10350** of **15957** in total

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Disease ID	Disease Name	Gene Symbol ▼	Gene ID	Organism	Source
DOID:3319	lymphangioleiomyomatosis Aliases: lung lymphangioleiomyomatosis lymphangiomyomatosis pulmonary lymphangioleiomyomatosis	ESBP6 TDH1 TDH2 TDH3	853106 853395 853465 855598	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0070353	cataract 47 Aliases: CTRCT47	ESBP6 MCH4 MCH5	854030 854483 855598	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:299	adenocarcinoma	ERS1	850438	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:1062	Fanconi syndrome Aliases: Congenital Fanconi syndrome De Toni-Fanconi syndrome Fanconi-de Toni syndrome Fanconi-de-Toni syndrome Infantile nephropathic cystinosis Lignac-Fanconi syndrome adult Fanconi Anemia adult Fanconi syndrome deToni Fanconi syndrome	ERS1	850438	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0110934	nemaline myopathy 7 Aliases: NEM7 nemaline myopathy 7, autosomal recessive	ERS1	850438	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:1064	cystinosis Aliases: cystine storage disease	ERS1	850438	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:305	carcinoma Aliases: epithelial cancer epithelioma malignant Epithelioma	ERS1 PHO8	850438 852092	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:326	ischemia	ERS1 MSL5	850438 850807	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:219	colon cancer	ERS1 GPX1 GPX2 PBS2	850438 852546 853313 853842	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0070214	familial hyperinsulinemic hypoglycemia 7 Aliases: EIHI HHF7 exercise-induced hyperinsulinemic hypoglycemia exercise-induced hyperinsulinism hyperinsulinism due to SLC16A1 deficiency hyperinsulinism due to monocarboxylate transporter 1 deficiency	ERS1 ESBP6	850438 855598	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:8557	oropharynx cancer Aliases: Oropharyngeal carcinoma malignant Oropharyngeal tumor malignant tumor of oropharynx malignant tumour of mesopharynx oropharyngeal cancer	ERN1	2081	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110771	hereditary spastic paraplegia 18 Aliases: IDMDC SPG18 autosomal recessive spastic paraplegia 18 autosomal recessive spastic paraplegia type 18 intellectual disability, motor dysfunction and joint contractures	ERLIN2	11160	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110813	hereditary spastic paraplegia 62 Aliases: SPG62 autosomal recessive spastic paraplegia 62 autosomal recessive spastic paraplegia type 62	ERLIN1	10613	Homo sapiens (human)	Alliance of Genome Resources
DOID:0090124	neurogenic-type arthrogryposis multiplex congenita-2 Aliases: AMC neurogenic type AMC2 AMCN arthrogryposis multiplex congenita 2, neurogenic type arthrogryposis multiplex congenita neurogenic type	ERGIC1	57222	Homo sapiens (human)	Alliance of Genome Resources
DOID:869	cholesteatoma	EREG HGF IL1A MMP2 MMP9 STAT4 TLR2 TLR4 VEGFA	2069 3082 3552 4313 4318 6775 7097 7099 7422	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080908	Cockayne syndrome B Aliases: Cockayne syndrome 2 Cockayne syndrome type II	ERCC6	2074	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080868	primary ovarian insufficiency 11	ERCC6	2074	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080911	cerebrooculofacioskeletal syndrome 1	ERCC6	2074	Homo sapiens (human)	Alliance of Genome Resources
DOID:0112158	De Sanctis-Cacchione syndrome Aliases: xeroderma pigmentosum with neurologic manifestation	ERCC6	2074	Homo sapiens (human)	Alliance of Genome Resources
DOID:14184	polyneuropathy due to drug	ERCC6	2074	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060240	UV-sensitive syndrome	ERCC6	2074	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110028	age related macular degeneration 5 Aliases: ARMD5	ERCC6	2074	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110849	xeroderma pigmentosum group G Aliases: XP group G XP7 XPG xeroderma pigmentosum VII	ERCC5	2073	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080913	cerebrooculofacioskeletal syndrome 3	ERCC5	2073	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050117	disease by infectious agent Aliases: infectious disease	ERCC5 MBL2 SERPIND1	2073 3053 4153	Homo sapiens (human)	Alliance of Genome Resources

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