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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 14476 - 14500 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲ Source
DOID:7474
  • malignant pleural mesothelioma
  • Aliases:
    • malignant mesothelioma of pleura
Saccharomyces cerevisiae S288C
DOID:0111630
  • familial erythrocytosis 8
  • Aliases:
    • BPGM deficiency
    • DPGM deficiency
    • ECYT8
    • bisphosphoglycerate mutase deficiency
    • bisphosphoglyceromutase deficiency
    • diphosphoglycerate mutase deficiency of erythrocyte
    • hemolytic anemia due to diphosphoglycerate mutase deficiency
Saccharomyces cerevisiae S288C
DOID:1825
  • childhood absence epilepsy
  • Aliases:
    • petit mal seizure
    • pyknolepsy
Saccharomyces cerevisiae S288C
DOID:585
  • nephrolithiasis
  • Aliases:
    • Stone - kidney/ureter
    • kidney stones
Saccharomyces cerevisiae S288C
DOID:14525
  • Reye syndrome
  • Aliases:
    • Reye's syndrome
Saccharomyces cerevisiae S288C
DOID:1967
  • leiomyosarcoma
  • Aliases:
    • Leiomyosarcomas
Saccharomyces cerevisiae S288C
DOID:2917
  • cryoglobulinemia
  • Aliases:
    • Cryoimmunoglobulinaemia
Saccharomyces cerevisiae S288C
DOID:750
  • peptic ulcer disease
  • Aliases:
    • acute peptic ulcer with hemorrhage
    • acute peptic ulcer with hemorrhage and perforation
    • acute peptic ulcer without hemorrhage and without perforation
Saccharomyces cerevisiae S288C
DOID:9277
  • primary cerebellar degeneration
Saccharomyces cerevisiae S288C
DOID:0110861
  • autosomal recessive polycystic kidney disease
  • Aliases:
    • Arpkd
    • Pkhd1
    • Polycystic Kidney Disease, Infantile, Type I
    • Polycystic Kidney and Hepatic Disease 1
Saccharomyces cerevisiae S288C
DOID:783
  • end stage renal disease
  • Aliases:
    • end stage renal failure
    • end-stage kidney disease
Saccharomyces cerevisiae S288C
DOID:0111403
  • mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations
  • Aliases:
    • MCCCHCM
Saccharomyces cerevisiae S288C
DOID:0110914
  • infantile hypophosphatasia
  • Aliases:
    • Hops
    • phosphoethanolaminuria
Saccharomyces cerevisiae S288C
DOID:0050883
  • infantile cerebellar-retinal degeneration
Saccharomyces cerevisiae S288C
DOID:0080552
  • congenital disorder of glycosylation Ia
  • Aliases:
    • PMM2-congenital disorder of glycosylation
    • congenital disorder of glycosylation 1a
Saccharomyces cerevisiae S288C
DOID:2739
  • Gilbert syndrome
  • Aliases:
    • Constitutional hyperbilirubinemia
    • Gilbert's disease
    • Gilbert's syndrome
    • Gilbert-Meulengracht syndrome
    • hereditary nonhemolytic jaundice
Saccharomyces cerevisiae S288C
DOID:0080562
  • congenital disorder of glycosylation Ij
  • Aliases:
    • Congenital disorder of glycosylation 1j
Saccharomyces cerevisiae S288C
DOID:0080909
  • castration-resistant prostate carcinoma
Saccharomyces cerevisiae S288C
DOID:0080630
  • B-lymphoblastic leukemia/lymphoma
  • Aliases:
    • B lymphoblastic leukemia/lymphoma
    • B-ALL
    • precursor B lymphoblastic lymphoma/leukemia
Saccharomyces cerevisiae S288C
DOID:3659
  • sialuria
Saccharomyces cerevisiae S288C
DOID:0070112
  • Niemann-Pick disease type B
Saccharomyces cerevisiae S288C
DOID:417
  • autoimmune disease
  • Aliases:
    • autoimmune hypersensitivity disease
    • hypersensitivity reaction type II disease
Saccharomyces cerevisiae S288C
DOID:9884
  • muscular dystrophy
Saccharomyces cerevisiae S288C
DOID:13628
  • favism
Saccharomyces cerevisiae S288C
DOID:2223
  • platelet storage pool deficiency
  • Aliases:
    • Dense body defect
    • Platelet dense granule deficiency
    • Platelet storage pool defect
Saccharomyces cerevisiae S288C
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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