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GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB), DisGeNET, and Alliance of Genome Resources is integrated into one list.

Source	Last Updated
Alliance of Genome Resources	July 29, 2024
DisGeNET	July 29, 2024
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **2001 - 2025** of **7942** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism ▼
DOID:2247	spondylosis Aliases: Lumbar spondylosis with myelopathy Spondylogenic compression of lumbar spinal cord Spondylogenic compression of thoracic spinal cord Thoracic or lumbar spondylosis with myelopathy lumbosacral spondylosis without myelopathy spondylosis with myelopathy	Kl	16591	Mus musculus (house mouse)
DOID:0080176	meningococcal meningitis	Tlr2 Tlr4	21898 24088	Mus musculus (house mouse)
DOID:13078	eumycotic mycetoma Aliases: Madura foot Maduromycosis, mycotic Mycotic mycetoma eumycetoma maduromycosis	Comt	12846	Mus musculus (house mouse)
DOID:1749	squamous cell carcinoma Aliases: epidermoid carcinoma malignant squamous cell tumor squamous carcinoma squamous cell Epithelioma squamous cell cancer	Trp53	22059	Mus musculus (house mouse)
DOID:4795	GM2 gangliosidosis, AB variant Aliases: Tay-Sachs disease AB variant Tay-Sachs disease, variant AB	Gm2a	14667	Mus musculus (house mouse)
DOID:0090129	carnitine palmitoyltransferase I deficiency Aliases: CPT I deficiency CPT1A deficiency L-CPT1 deficiency carnitine palmitoyl transferase 1A deficiency carnitine palmitoyl transferase IA deficiency hepatic CPT deficiency type I hepatic carnitine palmitoyl transferase 1 deficiency hepatic carnitine palmitoyl transferase I deficiency	Cpt1a	12894	Mus musculus (house mouse)
DOID:12783	migraine without aura Aliases: common migraine	Eno2 Tnf	13807 21926	Mus musculus (house mouse)
DOID:11396	pulmonary edema	Tnf	21926	Mus musculus (house mouse)
DOID:0060001	withdrawal disorder	Comt Htr2a	12846 15558	Mus musculus (house mouse)
DOID:11446	sciatic neuropathy	Gsk3b Hmgb1 Kcnj11 Pcna Ppargc1a Tlr4 Tnf	15289 16514 18538 19017 21898 21926 56637	Mus musculus (house mouse)
DOID:1920	hyperuricemia Aliases: Blood urate raized uricacidemia	Ins1 Ins2	16333 16334	Mus musculus (house mouse)
DOID:783	end stage renal disease Aliases: end stage renal failure end-stage kidney disease	Adipoq Cpt1a Enpp1 Kl Lep Pgf Tlr2 Tlr4 Tnf Ucp2	11450 12894 16591 16846 18605 18654 21898 21926 22228 24088	Mus musculus (house mouse)
DOID:9974	drug dependence	Comt	12846	Mus musculus (house mouse)
DOID:12401	intermittent explosive disorder Aliases: explosive personality disorder	Comt	12846	Mus musculus (house mouse)
DOID:0060075	estrogen-receptor positive breast cancer	Pik3ca	18706	Mus musculus (house mouse)
DOID:0080037	Worth syndrome Aliases: Worth's syndrome autosomal dominant endosteal hyperostosis autosomal dominant osteosclerosis benign form of Worth hyperostosis corticalis generalisata with torus platinus	Lrp5	16973	Mus musculus (house mouse)
DOID:0080410	familial adenomatous polyposis 2 Aliases: MUTYH-associated polyposis MUTYH-related attenuated FAP MUTYH-related attenuated familial adenomatous polyposis MUTYH-related attenuated familial polyposis coli	Mutyh	70603	Mus musculus (house mouse)
DOID:0110274	autosomal recessive limb-girdle muscular dystrophy	Poglut1 Pomt2	217734 224143	Mus musculus (house mouse)
DOID:0081427	autosomal recessive distal hereditary motor neuronopathy 8 Aliases: SORDD sorbitol dehydrogenase deficiency with peripheral neuropathy	Sord	20322	Mus musculus (house mouse)
DOID:0112216	developmental and epileptic encephalopathy 80 Aliases: DEE80 GPIBD20 early infantile epileptic encephalopathy 80 glycosylphosphatidylinositol biosynthesis defect 20	Pigb	55981	Mus musculus (house mouse)
DOID:0050902	medulloblastoma Aliases: CNS PNET CPNET Medulloblastoma, histologically defined brain medulloblastoma infratentorial primitive neuroectodermal tumor localized primitive neuroectodermal tumor	Trp53	22059	Mus musculus (house mouse)
DOID:0111240	congenital muscular dystrophy-dystroglycanopathy type A2 Aliases: MDDGA2 Walker-Warburg syndrome or muscle-eye-brain disease, POMT2-related congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A2	Pomt2	217734	Mus musculus (house mouse)
DOID:12466	secondary hyperparathyroidism	Kl	16591	Mus musculus (house mouse)
DOID:0060224	atrial fibrillation Aliases: A-fib AFib	Kcnq1 Tlr2 Tnf	16535 21926 24088	Mus musculus (house mouse)
DOID:326	ischemia	Akt2 Trp53	11652 22059	Mus musculus (house mouse)

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