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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 **9776 - 9800** of **15957** in total

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Disease ID	Disease Name	Gene Symbol ▼	Gene ID	Organism	Source
DOID:4440	seminoma Aliases: Seminoma, Pure	Fas Fasl Inha Insr Jup Kcne1 Kcnq1 Kit Kras Pcna Pdgfra Pdpn Pou5f1 Smad4 Tymp Vegfa	14102 14103 14726 16322 16337 16480 16509 16535 16590 16653 17128 18538 18595 18999 22339 72962	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:8568	infectious mononucleosis Aliases: Filatov's disease Gammaherpesviral mononucleosis Monocytic angina Pfeiffer's disease glandular fever mononucleosis	Fas Fasl Foxp3 H2-Eb1 Il27 Sod2	14102 14103 14969 20371 20656 246779	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111095	Fanconi anemia complementation group A Aliases: FANCA	Fanca	14087	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:13636	Fanconi anemia Aliases: Fanconi anaemia Fanconi pancytopenia Fanconi panmyelopathy Fanconi's anaemia Fanconi's anemia	Fanca Flt3l Ifng Il10 Prf1 Tnf	14087 14256 15978 16153 18646 21926	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110055	amelogenesis imperfecta type 3A Aliases: ADHCAI amelogenesis imperfecta hypomineralization type amelogenesis imperfecta type III autosomal dominant amelogenesis imperfecta hypocalcification type	Fam83h	105732	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:2187	amelogenesis imperfecta	Fam20c	80752	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:10609	rickets Aliases: active rickets	Fam20c	80752	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050445	X-linked dominant hypophosphatemic rickets Aliases: Hypophosphatemia, Vitamin D-Resistant Rickets Vitamin D-Resistant Rickets, X-Linked X-linked hypophosphatemia hypophosphatemic rickets X-linked dominant	Fam20c Phex	18675 80752	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110066	amelogenesis imperfecta type 1G Aliases: AI1G AIGFS ERS amelogenesis imperfecta and gingival fibromatosis syndrome amelogenesis imperfecta hypoplastic with nephrocalcinosis amelogenesis imperfecta type IG enamel-renal syndrome enamel-renal-gingival syndrome	Fam20a	208659	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0070378	developmental and epileptic encephalopathy 109 Aliases: DEE109	FZR1	51343	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080079	nonsyndromic congenital nail disorder 1 Aliases: nonsyndromic congenital nail disorder 10 twenty-nail dystrophy	FZD6	8323	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060844	Norrie disease Aliases: Episkopi blindness Norrie-Warburg disease atrophia bulborum hereditaria	FZD4	8322	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111412	exudative vitreoretinopathy 1 Aliases: EVR1	FZD4	8322	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080845	omodysplasia 2	FZD2	2535	Homo sapiens (human)	Alliance of Genome Resources
DOID:0081344	congenital myopathy 9B	FXR1	8087	Homo sapiens (human)	Alliance of Genome Resources
DOID:0081343	congenital myopathy 9A	FXR1	8087	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111431	essential tremor 4 Aliases: ETM4 hereditary essential tremor 4	FUS	2521	Homo sapiens (human)	Alliance of Genome Resources
DOID:3382	liposarcoma Aliases: lipomatous cancer	FUS IL22	2521 50616	Homo sapiens (human)	Alliance of Genome Resources
DOID:14500	fucosidosis Aliases: A-fucosidase deficiency alpha fucosidase deficiency	FUCA1	2517	Homo sapiens (human)	Glyco-Disease Genes Database Alliance of Genome Resources
DOID:0112034	non-syndromic X-linked intellectual disability 9 Aliases: MRX44 MRX9 X-linked mental retardation 44 X-linked mental retardation 9	FTSJ1	24140	Homo sapiens (human)	Alliance of Genome Resources
DOID:13963	nuclear senile cataract Aliases: Senile nuclear cataract Senile nuclear sclerosis	FTO	79068	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080334	aortic valve disease 2	FTO LMNA MMP2 SMAD6	4000 4091 4313 79068	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111031	hemochromatosis type 5 Aliases: FTH1-associated iron overload FTH1-related iron overload HFE5	FTH1	2495	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060762	restrictive dermopathy Aliases: Infantile restrictive dermopathy Lethal tight skin contracture syndrome hyperkeratosis-contracture syndrome lethal restrictive dermopathy tight skin contracture syndrome	FST	10468	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111911	spermatogenic failure 34 Aliases: SPGF34	FSIP2	401024	Homo sapiens (human)	Alliance of Genome Resources

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