GlyCosmos Portal

Source	Last Updated
Alliance of Genome Resources	October 9, 2024
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **11026 - 11050** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▼	Organism	Source
DOID:1588	thrombocytopenia	gale-1 pat-2 pat-3	173171 175504 176240	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0060479	Shwachman-Diamond syndrome Aliases: Shwachman syndrome Shwachman-Bodian-Diamond syndrome Shwachman-Diamond type metaphyseal dysplasia pancreatic insufficiency and bone marrow dysfunction	eif-6 srp-1 srp-3 srp-6 srp-7	173169 178585 178672 179125 179195	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0111527	spinal muscular atrophy with progressive myoclonic epilepsy Aliases: Jankovic-Rivera syndrome SMA-PME SMAPME hereditary myoclonus-progressive distal muscular atrophy syndrome	asah-1 asah-2	173120 185021	Caenorhabditis elegans	Alliance of Genome Resources
DOID:1927	sphingolipidosis Aliases: sphingolipidoses	asah-1 asah-2	173120 185021	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0050464	Farber lipogranulomatosis Aliases: Farber disease N-laurylsphingosine deacylase deficiency acid ceramidase deficiency	asah-1 asah-2	173120 185021	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0110590	autosomal dominant nonsyndromic deafness 69 Aliases: DCUA DFNA69 autosomal dominant deafness 69 unilateral or asymmetric congenital deafness	Kitl	17311	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111373	familial progressive hyperpigmentation with or without hypopigmentation Aliases: FPHH MUH melanosis universalis hereditaria	Kitl	17311	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110242	cataract 13 with adult i phenotype Aliases: CTRCT13	gly-15 gly-16	173109 173114	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0081345	congenital myopathy 10B	ced-1	173064	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0111333	early-onset myopathy-areflexia-respiratory distress-dysphagia syndrome Aliases: EMARDD Myopathy, areflexia, respiratory distress, and dysphagia, early-onset congenital myopathy 10A	ced-1	173064	Caenorhabditis elegans	Alliance of Genome Resources
DOID:1289	neurodegenerative disease Aliases: degenerative disease	apl-1 ced-1 deg-1 eat-4 glr-1 glt-3 glt-4 mec-4 pkc-2 poml-1 ptc-1 ptc-3 tir-1 vglu-2 vglu-3	173064 173631 174274 175502 176204 176291 176441 176442 177882 180783 181035 181166 181728 187297 188744	Caenorhabditis elegans	Alliance of Genome Resources
DOID:9562	primary ciliary dyskinesia Aliases: ciliary motility disorder immotile ciliary syndrome	kpc-1	173051	Caenorhabditis elegans	Alliance of Genome Resources
DOID:14679	VACTERL association	grd-2 kpc-1 wrt-6	173051 180349 180638	Caenorhabditis elegans	Alliance of Genome Resources
DOID:234	colon adenocarcinoma Aliases: Colonic adenocarcinoma adenocarcinoma of colon	W01F3.2 kpc-1 rnst-2 ver-4 zmp-4	173051 179991 180351 186632 190096	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0050545	visceral heterotaxy Aliases: heterotaxia situs ambiguus	C14B9.8 daf-4 kpc-1	173051 175781 176149	Caenorhabditis elegans	Alliance of Genome Resources
DOID:11446	sciatic neuropathy	W01F3.2 cri-2 drag-1 eat-4 gpx-3 gpx-5 hyl-2 kpc-1 lmp-1 nlg-1 ver-1 vglu-2 vglu-3 zmp-2 zmp-4	173051 175182 175383 176291 176441 176442 179197 179991 180351 180743 180912 181178 181484 182513 190602	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0050861	colorectal adenocarcinoma	kpc-1 let-23 mnr-1 pgp-1 pgp-3 rnst-2 tpst-1 ver-1 ver-4	173051 174462 175182 176684 178215 180350 181326 186632 190096	Caenorhabditis elegans	Alliance of Genome Resources
DOID:13375	temporal arteritis Aliases: Horton's disease giant cell arteritis	W01F3.2 cht-1 spe-9 zmp-4	173042 179991 180351 180628	Caenorhabditis elegans	Alliance of Genome Resources
DOID:799	varicose veins Aliases: Varix Venous ectasia Venous varices varices	W01F3.2 lron-5 spe-9 zmp-3 zmp-4	173042 178748 179991 180351 184307	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0050852	limb ischemia	cts-1 spe-9	173042 176437	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0060227	Adams-Oliver syndrome Aliases: Adams Oliver syndrome	H12D21.10 glp-1 spe-9	173042 176286 179990	Caenorhabditis elegans	Alliance of Genome Resources
DOID:5241	hemangioblastoma Aliases: Capillary Hemangioblastoma	glp-1 lin-12 spe-9	173042 176282 176286	Caenorhabditis elegans	Alliance of Genome Resources
DOID:264	hemangiopericytoma Aliases: Haemangiopericytic meningioma hemangiopericytoma, malignant malignant hemangiopericytoma	glp-1 lin-12 spe-9 vab-1 ver-1 ver-4	173042 173794 175182 176282 176286 186632	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0110274	autosomal recessive limb-girdle muscular dystrophy	lam-3	172952	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0110636	congenital merosin-deficient muscular dystrophy 1A Aliases: CMD1A MDC1A Merosin-negative congenital muscular dystrophy congenital muscular dystrophy due to laminin alpha2 deficiency	lam-3	172952	Caenorhabditis elegans	Alliance of Genome Resources

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