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 7651 - 7675 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:12241
  • beta thalassemia
Homo sapiens (human)
DOID:2920
  • membranoproliferative glomerulonephritis
  • Aliases:
    • Lobular glomerulonephritis
    • chronic glomerulonephritis, lobular
Homo sapiens (human)
DOID:0111108
  • maturity-onset diabetes of the young type 10
  • Aliases:
    • MODY10
Homo sapiens (human)
DOID:0060480
  • left ventricular noncompaction
  • Aliases:
    • left ventricular hypertrabeculation
Mus musculus (house mouse)
DOID:0081394
  • Caroli syndrome
Mus musculus (house mouse)
DOID:0112282
  • spondyloepiphyseal dysplasia Kimberley type
  • Aliases:
    • SEDK
Mus musculus (house mouse)
DOID:674
  • cleft palate
  • Aliases:
    • Palatoschisis
Homo sapiens (human)
DOID:559
  • acute pyelonephritis
Homo sapiens (human)
DOID:13515
  • tuberous sclerosis
  • Aliases:
    • Bourneville's disease
    • Epiloia
    • Tuberose sclerosis
    • Tuberous sclerosis syndrome
    • cerebral sclerosis
Drosophila melanogaster (fruit fly)
DOID:13328
  • diabetic cataract
  • Aliases:
    • Cataract - diabetic
Saccharomyces cerevisiae S288C
DOID:1380
  • endometrial cancer
  • Aliases:
    • endometrial Ca
    • endometrial neoplasm
    • malignant endometrial neoplasm
    • malignant neoplasm of endometrium
    • neoplasm of endometrium
    • primary malignant neoplasm of endometrium
    • tumor of Endometrium
Mus musculus (house mouse)
DOID:0081141
  • agammaglobulinemia 9
Saccharomyces cerevisiae S288C
DOID:0110160
  • Charcot-Marie-Tooth disease axonal type 2T
  • Aliases:
    • AR-CMT2T
    • CMT2T
    • Charcot-Marie-Tooth neuropathy type 2T
    • autosomal recessive axonal Charcot-Marie-Tooth disease type 2T
Homo sapiens (human)
DOID:0111441
  • optic atrophy 1
  • Aliases:
    • OPA1
Homo sapiens (human)
DOID:0110721
  • neuronal ceroid lipofuscinosis 1
  • Aliases:
    • CLN1
    • neuronal ceroid lipofuscinosis 1 variable age of onset
Mus musculus (house mouse)
DOID:0112186
  • thyroid dyshormonogenesis 2A
  • Aliases:
    • TDH2A
    • genetic defect in thyroid hormonogenesis 2A
    • iodide peroxidase deficiency
    • thyroid peroxidase deficiency
Homo sapiens (human)
DOID:986
  • alopecia areata
  • Aliases:
    • Circumscribed alopecia
Mus musculus (house mouse)
DOID:11520
  • benign hypertensive renal disease
  • Aliases:
    • hypertensive renal disease, benign
    • hypertensive renal disease, benign, without mention of renal failure
Homo sapiens (human)
DOID:0090056
  • dystonia 12
Drosophila melanogaster (fruit fly)
DOID:3908
  • lung non-small cell carcinoma
  • Aliases:
    • NSCLC
    • Non-small cell lung cancer
    • non-small cell lung carcinoma
Caenorhabditis elegans
DOID:13533
  • osteopetrosis
  • Aliases:
    • Albers-Schonberg disease
    • marble bone
Caenorhabditis elegans
DOID:2986
  • IgA glomerulonephritis
  • Aliases:
    • Berger's IgA or IgG nephropathy
    • Focal Glomerulonephritis
    • IgA nephropathy
    • primary IgA nephropathy
    • segmental glomerulonephritis
Xenopus laevis (African clawed frog)
DOID:10685
  • separation anxiety disorder
Danio rerio (zebrafish)
DOID:0111141
  • delayed sleep phase syndrome
  • Aliases:
    • DSPD
Mus musculus (house mouse)
DOID:0080554
  • congenital disorder of glycosylation Ib
  • Aliases:
    • congenital disorder of glycosylation 1b
Rattus norvegicus (Norway rat)

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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: December 9, 2024