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 1151 - 1175 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼ Source
DOID:0080470
  • developmental and epileptic encephalopathy 36
  • Aliases:
    • congenital disorder of glycosylation, type Is
    • early infantile epileptic encephalopathy 36
Saccharomyces cerevisiae S288C
DOID:0110669
  • congenital myasthenic syndrome 14
  • Aliases:
    • CMS14
    • CMSTA3
    • congenital myasthenic syndrome 14, with tubular aggregates
    • congenital myasthenic syndrome with tubular aggregates 3
Saccharomyces cerevisiae S288C
DOID:1324
  • lung cancer
Saccharomyces cerevisiae S288C
DOID:14323
  • Marfan syndrome
  • Aliases:
    • Marfan's syndrome
Saccharomyces cerevisiae S288C
DOID:3910
  • lung adenocarcinoma
  • Aliases:
    • bronchogenic lung adenocarcinoma
    • nonsmall cell adenocarcinoma
Saccharomyces cerevisiae S288C
DOID:13317
  • hyperinsulinemic hypoglycemia
  • Aliases:
    • Islet cell hyperplasia
    • nesidioblastosis
    • persistent hyperinsulinemia hypoglycemia of infancy
Saccharomyces cerevisiae S288C
DOID:0060081
  • triple-receptor negative breast cancer
Saccharomyces cerevisiae S288C
DOID:13268
  • porphyria
  • Aliases:
    • Hematoporphyria
    • Porphyrinopathy
    • disorder of porphyrin and hem metabolism
    • disorder of porphyrin metabolism
Saccharomyces cerevisiae S288C
DOID:0111155
  • autosomal recessive spinocerebellar ataxia 21
  • Aliases:
    • SCAR21
    • acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome
    • autosomal recessive spinocerebellar ataxia 21 with hepatopathy
Saccharomyces cerevisiae S288C
DOID:3892
  • insulinoma
  • Aliases:
    • Insulin-Producing tumor of Islet cells
    • Islet cell adenoma
Saccharomyces cerevisiae S288C
DOID:0060466
  • gingival fibromatosis
  • Aliases:
    • hereditary gingival fibromatosis
    • hereditary gingival hyperplasia
Saccharomyces cerevisiae S288C
DOID:0070185
  • X-linked spermatogenic failure 2
  • Aliases:
    • SPGFX2
Saccharomyces cerevisiae S288C
DOID:1100
  • ovarian disease
Saccharomyces cerevisiae S288C
DOID:0110725
  • neuronal ceroid lipofuscinosis 10
  • Aliases:
    • CLN10
    • Cathepsin D deficiency
    • neuronal ceroid lipofuscinosis cathepsin D-deficient
    • neuronal ceroid lipofuscinosis due to cathepsin D deficiency
Saccharomyces cerevisiae S288C
DOID:0050645
  • arterial tortuosity syndrome
Saccharomyces cerevisiae S288C
DOID:0110914
  • infantile hypophosphatasia
  • Aliases:
    • Hops
    • phosphoethanolaminuria
Saccharomyces cerevisiae S288C
DOID:591
  • phobic disorder
Saccharomyces cerevisiae S288C
DOID:0050644
  • arterial calcification of infancy
  • Aliases:
    • generalized arterial calcification of infancy
    • idiopathic infantile arterial calcification
    • infantile arteriosclerosis
Saccharomyces cerevisiae S288C
DOID:2349
  • arteriosclerosis
  • Aliases:
    • Arteriosclerotic vascular disease
Saccharomyces cerevisiae S288C
DOID:8719
  • in situ carcinoma
Saccharomyces cerevisiae S288C
DOID:9538
  • multiple myeloma
  • Aliases:
    • myeloma
Saccharomyces cerevisiae S288C
DOID:10003
  • sensorineural hearing loss
  • Aliases:
    • High Frequency Hearing Loss
    • High frequency deafness
    • Perceptive deafness
    • Perceptive hearing loss
    • Perceptive hearing loss or deafness
    • Sensorineural Deafness
    • Sensory hearing loss
    • central hearing loss
    • high-frequency hearing loss
Saccharomyces cerevisiae S288C
DOID:0112333
  • pontocerebellar hypoplasia type 16
  • Aliases:
    • PCH16
Saccharomyces cerevisiae S288C
DOID:10976
  • membranous glomerulonephritis
  • Aliases:
    • membranous nephropathy
Saccharomyces cerevisiae S288C
DOID:0111030
  • hemochromatosis type 3
  • Aliases:
    • HFE3
    • TFR2-related hemochromatosis
    • hemochromatosis due to defect in transferrin receptor 2
Saccharomyces cerevisiae S288C

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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