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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 **6976 - 7000** of **15957** in total

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Disease ID	Disease Name	Gene Symbol ▼	Gene ID	Organism	Source
DOID:0080746	Sweet syndrome Aliases: Acute Febrile Neutrophilic Dermatosis Sweet's syndrome	Mmp2 Mmp9	81686 81687	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0111563	Sturge-Weber syndrome Aliases: SWS Sturge-Weber-Dimitri syndrome Sturge-Weber-Krabbe angiomatosis Sturge-Weber-Krabbe syndrome encephalofacial angiomatosis encephalotrigeminal angiomatosis fourth phacomatosis leptomeningeal angiomatosis meningeal capillary angiomatosis	Mmp2 Mmp9	81686 81687	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:255	hemangioma	Mmp2 Slc2a1	17390 20525	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:8553	pyoderma gangrenosum	Mmp2 Mmp9	17390 17395	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080746	Sweet syndrome Aliases: Acute Febrile Neutrophilic Dermatosis Sweet's syndrome	Mmp2 Mmp9	17390 17395	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080933	immunoglobulin light chain amyloidosis Aliases: AL amyloidosis Amyloidosis primary systemic Light chain amyloidosis Primary AL amyloidosis Primary systemic AL amyloidosis Primary systemic amyloidosis Systemic AL amyloidsis	Mmp1a Mmp2	17390 83995	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080030	spondyloepimetaphyseal dysplasia, Missouri type	Mmp13	17386	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:3362	coronary aneurysm Aliases: Aneurysm of coronary vessels Aneurysmal lesion of coronary artery Arteriovenous aneurysm of coronary vessels	Mmp12	117033	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0111745	cerebellar ataxia type 43 Aliases: SCA43	Mme	24590	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0110160	Charcot-Marie-Tooth disease axonal type 2T Aliases: AR-CMT2T CMT2T Charcot-Marie-Tooth neuropathy type 2T autosomal recessive axonal Charcot-Marie-Tooth disease type 2T	Mme	24590	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:13250	diarrhea	Mme Slc26a3	114629 24590	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0111745	cerebellar ataxia type 43 Aliases: SCA43	Mme	17380	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110160	Charcot-Marie-Tooth disease axonal type 2T Aliases: AR-CMT2T CMT2T Charcot-Marie-Tooth neuropathy type 2T autosomal recessive axonal Charcot-Marie-Tooth disease type 2T	Mme	17380	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:13250	diarrhea	Mme Slc26a3	13487 17380	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:8864	acute monocytic leukemia Aliases: acute Monoblastic Leukemia and acute Monocytic Leukemia acute monocytic leukaemia acute monocytic leukaemia without mention of remission acute monocytic leukemia without mention of remission acute monocytic leukemia, FAB M5 acute monocytic leukemia, morphology	Mllt10	17354	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050465	Muir-Torre syndrome	Mlh1	17350	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0070274	hereditary nonpolyposis colorectal cancer type 2 Aliases: COCA2 FCC2 HNPCC2 familial nonpolyposis colon cancer type 2	Mlh1	17350	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0112182	mismatch repair cancer syndrome Aliases: BTP1 syndrome BTPS1 CMMR-D syndrome CMMRDS MMR deficiency Turcot syndrome brain tumor-polyposis syndrome 1 childhood cancer syndrome constitutional mismatch repair deficiency syndrome	Mlh1 Msh6 Rnaset2a Rnaset2b Slc22a19 Slc22a26 Slc22a27 Slc22a28 Slc22a29 Slc22a30 Tgfbr2 Trp53	100037283 171405 17350 17688 207151 21813 22059 236149 236293 319800 434674 68195	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:5031	adult pineal parenchymal tumor Aliases: adult Pineal Parenchymal neoplasm	Mki67	17345	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110950	Waardenburg syndrome type 2A Aliases: WS2A Waardenburg syndrome type IIA	Mitf	17342	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110948	Waardenburg syndrome type 1 Aliases: WS1 Waardenburg syndrome type I	Mitf	17342	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0090100	ocular albinism with sensorineural deafness Aliases: WS2-OA autosomal recessive Waardenburg syndrome type 2 with ocular albinism digenic Waardenburg syndrome/albinism digenic Waardenburg syndrome/ocular albinism	Mitf	17342	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0090002	Tietz syndrome Aliases: Tietz albinism-deafness syndrome albinism-deafness of Tietz hypopigmentation/deafness of Tietz	Mitf	17342	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:14021	Tietze's syndrome Aliases: Costalchondritis Costochondral junction syndrome Costochondritis Slipping rib syndrome Tietze's disease	Mitf	17342	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:4997	Camurati-Engelmann disease Aliases: Diaphyseal dysplasia Engelman's disease progressive diaphyseal dysplasia	Mitf Tgfb1	17342 21803	Mus musculus (house mouse)	Alliance of Genome Resources

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