GlyCosmos Portal

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

Displaying entries **15801 - 15825** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism ▼	Source
DOID:0110122	Axenfeld-Rieger syndrome type 3 Aliases: Axenfeld-Rieger anomaly with or without cardiac defects and/or sensorineural hearing loss RIEG3 Rieger syndrome type 3 anterior chamber cleavage syndrome anterior segment mesenchymal dysgenesis	dbl-1	179068	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0111678	hereditary folate malabsorption Aliases: congenital defect of folate absorption congenital folate malabsorption	slc-46A	189356	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0070422	syndromic X-linked intellectual disability Pilorge type Aliases: MRXSP	glc-1 glc-2	172103 180086	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0060240	UV-sensitive syndrome	csa-1	174474	Caenorhabditis elegans	Alliance of Genome Resources
DOID:2843	long QT syndrome Aliases: LQT long Q-T syndrome	unc-103	175527	Caenorhabditis elegans	Alliance of Genome Resources
DOID:18	urinary system disease Aliases: Non-neoplastic urinary tract disease urinary tract disease	dbl-1	179068	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0060774	congenital diarrhea	cwn-2	177870	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0050851	glomerulosclerosis	W01F3.2 acn-1 zmp-2 zmp-4	175383 179991 180351 180780	Caenorhabditis elegans	Alliance of Genome Resources
DOID:9970	obesity	C06G1.1 C27A7.3 C49C8.5 W01C8.5 W01F3.2 abt-2 acn-1 apl-1 asp-1 cnx-1 cpd-2 cpi-1 cri-2 cwn-1 daf-2 dat-1 dhrr-1 dop-1 dop-2 dsc-4 egl-21 eif-6 enpp-1 gcy-27 glp-1 gon-1 gpd-1 gpd-3 gpd-4 gpx-3 gpx-5 gspd-1 hda-4 let-2 lev-9 lin-44 nhx-3 nhx-9 nkb-1 nkb-3 npr-17 pkc-2 poml-1 poml-2 ptp-3 rig-4 scav-1 sdn-1 skn-1 stim-1 zmp-4	171782 171994 171999 173169 173399 174578 174603 174685 175201 175410 176124 176286 176304 176390 176852 177343 177372 177597 177668 177850 177940 178046 178126 179197 179347 179663 179665 179991 180251 180351 180601 180714 180780 180783 180812 180836 181166 181178 181259 181494 181684 181708 181720 181723 182513 182726 183811 187297 188252 191374 191654	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0060210	amyotrophic lateral sclerosis type 19 Aliases: ALS19 amyotrophic lateral sclerosis 19	let-23	174462	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0112189	thyroid dyshormonogenesis 6 Aliases: TDH6 genetic defect in thyroid hormonogenesis 6	bli-3 duox-2	171608 186188	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0070222	progressive familial intrahepatic cholestasis 2 Aliases: BSEP deficiency PFIC2	pgp-1 pgp-3	178215 181326	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0060669	cerebral cavernous malformation Aliases: cavernous angiomatous malformations cerebral capillary malformations familial cavernous angioma	poml-1 poml-2 ver-1 ver-3 ver-4	171999 175182 181289 186632 187297	Caenorhabditis elegans	Alliance of Genome Resources
DOID:9408	acute myocardial infarction	gpx-3 gpx-5	181178 182513	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0090050	dystonia 27	R193.2	182256	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0080348	Alzheimer's disease 1 Aliases: Alzheimer's disease 1, early onset	apl-1 pxn-1 pxn-2	180783 181288 191484	Caenorhabditis elegans	Alliance of Genome Resources
DOID:10964	cholesteatoma of middle ear Aliases: Cholesteatoma of middle ear and mastoid Cholesteatoma of middle ear and/or mastoid Cholesteatoma of the middle ear Epidermosis of ear Epidermosis of middle ear middle ear cholesteatoma	W01F3.2 zmp-3 zmp-4	178748 179991 180351	Caenorhabditis elegans	Alliance of Genome Resources
DOID:5409	lung small cell carcinoma	acr-2 acr-3 cdh-4 daf-1 epi-1 glp-1 lam-1 lam-2 lev-1 pat-3 sma-6 unc-38 unc-63 ver-4	172105 172150 174044 175504 175590 176286 176829 177292 177956 178269 180936 180937 180980 186632	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0110680	congenital myasthenic syndrome 2C Aliases: CMS2C congenital myasthenic syndrome 2C associated with acetylcholine receptor deficiency	acr-3 unc-63	172150 180937	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0050787	juvenile polyposis syndrome	daf-4 sma-6	174044 175781	Caenorhabditis elegans	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	daf-4 rnst-2	175781 190096	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0111029	hemochromatosis type 1 Aliases: HFE1 symptomatic form of HFE-related hereditary hemochromatosis symptomatic form of classic hemochromatosis symptomatic form of hemochromatosis type 1	dbl-1	179068	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0080470	developmental and epileptic encephalopathy 36 Aliases: congenital disorder of glycosylation, type Is early infantile epileptic encephalopathy 36	algn-13	179890	Caenorhabditis elegans	Alliance of Genome Resources
DOID:4250	conjunctivochalasis	W01F3.2 zmp-3 zmp-4	178748 179991 180351	Caenorhabditis elegans	Alliance of Genome Resources
DOID:4948	gallbladder carcinoma Aliases: cancer of the gallbladder carcinoma gallbladder carcinoma of gallbladder	T13H5.8 gpx-3 gpx-5 ptc-1 ptc-3	173631 174274 174362 181178 182513	Caenorhabditis elegans	Alliance of Genome Resources

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