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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 **6851 - 6875** of **15957** in total

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Disease ID	Disease Name	Gene Symbol ▼	Gene ID	Organism	Source
DOID:0060651	MYH-9 related disease	Myh9	17886	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110548	autosomal dominant nonsyndromic deafness 17 Aliases: DFNA17 autosomal dominant deafness 17	Myh9	17886	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111268	autosomal recessive hyaline body myopathy Aliases: MSMB Myopathy, myosin storage, autosomal recessive congenital myopathy 7B	Myh7	140781	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0070197	distal myopathy 1 Aliases: Distal myopathy type 1 Gowers disease Laing distal myopathy Laing early-onset distal myopathy MPD1	Myh7	140781	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110307	hypertrophic cardiomyopathy 1 Aliases: CMH1 cardiomyopathy, familial hypertrophic 1 hypertrophic cardiomyopathy 19	Myh7	140781	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110320	hypertrophic cardiomyopathy 14 Aliases: CMH14 cardiomyopathy familial hypertrophic 14	Myh6	17888	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110108	atrial heart septal defect 3 Aliases: ASD3 atrial septal defect 3	Myh6	17888	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110453	dilated cardiomyopathy 1EE Aliases: CMD1EE	Myh6	17888	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111599	distal arthrogryposis type 2B Aliases: DA2B Freeman-Sheldon syndrome variant Sheldon-Hall syndrome	Myh3	17883	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0081321	contractures, pterygia, and spondylocarpotarsal fusion syndrome 1A Aliases: Autosomal dominant multiple pterygium syndrome	Myh3	17883	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0081322	contractures, pterygia, and spondylocarpotarsal fusion syndrome 1B Aliases: Autosomal recessive multiple pterygium syndrome	Myh3	17883	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111596	distal arthrogryposis type 1 Aliases: DA1 digitotalar dysmorphism	Myh13 Myh1 Myh2 Myh3 Myh4 Myh6 Myh7 Myh7b	140781 17879 17882 17883 17884 17888 544791 668940	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111605	distal arthrogryposis type 2A Aliases: DA2A distal arthrogryposis type 2A (Freeman-Sheldon)	Myh13 Myh1 Myh2 Myh3 Myh4 Myh6 Myh7 Myh7b	140781 17879 17882 17883 17884 17888 544791 668940	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:2106	myotonia congenita Aliases: Batten Turner congenital myopathy Thomsen and Becker disease	Myh13 Myh1 Myh2 Myh3 Myh4 Myh6 Myh7 Myh7b	140781 17879 17882 17883 17884 17888 544791 668940	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111269	autosomal dominant hyaline body myopathy Aliases: MSMA Myopathy, myosin storage, autosomal dominant congenital myopathy 7A myopathy with lysis of type I myofibrils	Myh13 Myh1 Myh2 Myh3 Myh4 Myh6 Myh7 Myh7b	140781 17879 17882 17883 17884 17888 544791 668940	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080719	congenital myopathy 6 Aliases: inclusion body myopathy 3 proximal myopathy and ophthalmoplegia	Myh13 Myh1 Myh2 Myh3 Myh4 Myh6 Myh7 Myh7b	140781 17879 17882 17883 17884 17888 544791 668940	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111602	distal arthrogryposis type 2B3 Aliases: DA2B3 distal arthrogryposis type 2B3 (Sheldon-Hall)	Myh13 Myh1 Myh2 Myh3 Myh4 Myh6 Myh7 Myh7b	140781 17879 17882 17883 17884 17888 544791 668940	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110454	dilated cardiomyopathy 1S Aliases: CMD1S	Myh13 Myh1 Myh2 Myh3 Myh4 Myh6 Myh7 Myh7b	140781 17879 17882 17883 17884 17888 544791 668940	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0060464	Feingold syndrome Aliases: FGLDS MODED syndrome ODED syndrome digital anomalies with short palpebral fissures and atresia of esophagus or duodenum microcephaly-digital anomalies-normal intelligence syndrome microcephaly-oculo-digito-esophageal-duodenal syndrome oculo-digito-esophageal-duodenal syndrome	Mycn	18109	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110858	polycystic kidney disease 1 Aliases: Apkd1 Pkd1 Polycystic Kidney Disease, Adult, Type I	Myc	24577	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:3672	rhabdoid cancer Aliases: Rhabdoid sarcoma malignant rhabdoid tumour	Myc	24577	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:8584	Burkitt lymphoma Aliases: Burkitt lymphoma/leukaemia Burkitt's Lymphoma Burkitt's tumor Burkitt's tumor or lymphoma malignant lymphoma, Burkitt's type small Non-Cleaved cell Lymphoma, Burkitt's type	Myc	24577	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0001816	angiosarcoma Aliases: hemangiosarcoma	Myc Tp53	24577 24842	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:5394	prolactinoma Aliases: PITUITARY ADENOMA, PROLACTIN-SECRETING Prolactinoma of Pituitary gland familial prolactinoma	Myc Npy5r Ptgs2	24577 25340 29527	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:1319	brain cancer Aliases: BT - Brain tumour adult brain tumor adult malignant brain neoplasm brain neoplasm brain neoplasm, adult malignant brain tumour malignant primary brain neoplasm malignant primary brain tumor malignant tumor of Brain malignant tumor of adult brain neoplasm of brain primary brain neoplasm primary brain tumor primary malignant neoplasm of brain tumor of the Brain	Myc Notch1 Notch3	24577 25496 56761	Rattus norvegicus (Norway rat)	Alliance of Genome Resources

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