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 6726 - 6750 of 7942 in total
Disease ID Disease Name ▲ Gene Symbol Gene ID Organism
DOID:1070
  • primary open angle glaucoma
  • Aliases:
    • chronic simple glaucoma
Saccharomyces cerevisiae S288C
DOID:1070
  • primary open angle glaucoma
  • Aliases:
    • chronic simple glaucoma
Homo sapiens (human)
DOID:1070
  • primary open angle glaucoma
  • Aliases:
    • chronic simple glaucoma
Mus musculus (house mouse)
DOID:5426
  • primary ovarian insufficiency
  • Aliases:
    • hypergonadotropic hypogonadism
    • premature ovarian failure
    • premature ovarian insufficiency
Homo sapiens (human)
DOID:0060280
  • primary pigmented nodular adrenocortical disease
Homo sapiens (human)
DOID:10780
  • primary polycythemia
  • Aliases:
    • Familiar Polycythemia
    • familial erythrocytosis
Homo sapiens (human)
DOID:0050784
  • primary progressive multiple sclerosis
  • Aliases:
    • PPMS
    • Primary-progressive MS
Homo sapiens (human)
DOID:14557
  • primary pulmonary hypertension
  • Aliases:
    • Idiopathic pulmonary arterial hypertension
Homo sapiens (human)
DOID:0060643
  • primary sclerosing cholangitis
Mus musculus (house mouse)
DOID:0060643
  • primary sclerosing cholangitis
Rattus norvegicus (Norway rat)
DOID:0060643
  • primary sclerosing cholangitis
Homo sapiens (human)
DOID:0080218
  • primary spontaneous pneumothorax
Homo sapiens (human)
DOID:649
  • prion disease
  • Aliases:
    • Prion disease pathway
    • Prion protein disease
    • Spongiform Encephalopathy
    • prion induced disorder
    • transmissible spongiform encephalopathy
Homo sapiens (human)
DOID:3127
  • proctitis
Homo sapiens (human)
DOID:3911
  • progeria
  • Aliases:
    • HGPS
    • Hutchinson Gilford syndrome
    • Hutchinson-Gilford Progeria syndrome
    • Hutchinson-Gilford disease
Mus musculus (house mouse)
DOID:3911
  • progeria
  • Aliases:
    • HGPS
    • Hutchinson Gilford syndrome
    • Hutchinson-Gilford Progeria syndrome
    • Hutchinson-Gilford disease
Homo sapiens (human)
DOID:681
  • progressive bulbar palsy
Homo sapiens (human)
DOID:0070226
  • progressive familial intrahepatic cholestasis 1
  • Aliases:
    • FIC1 deficiency
    • PFIC1
Homo sapiens (human)
DOID:0070224
  • progressive familial intrahepatic cholestasis 4
  • Aliases:
    • PFIC4
    • TJP2 deficit
Homo sapiens (human)
DOID:0070221
  • progressive familial intrahepatic cholestasis
  • Aliases:
    • PFIC; Byler disease
Homo sapiens (human)
DOID:643
  • progressive multifocal leukoencephalopathy
Homo sapiens (human)
DOID:318
  • progressive muscular atrophy
  • Aliases:
    • Pure progressive muscular atrophy
    • progressive spinal muscular atrophy
Homo sapiens (human)
DOID:0111452
  • progressive myoclonus epilepsy 1A
  • Aliases:
    • EPM1A
Homo sapiens (human)
DOID:0111444
  • progressive myoclonus epilepsy 4
  • Aliases:
    • AMRF
    • EPM4
    • Myoclonus-nephropathy syndrome
    • action myoclonus-renal failure syndrome
Homo sapiens (human)
DOID:0111451
  • progressive myoclonus epilepsy 8
  • Aliases:
    • EMP8
    • PME type 8
    • progressive myoclonic epilepsy due to CERS1 deficiency
    • progressive myoclonus epilepsy type 8
Homo sapiens (human)

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024