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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 7526 - 7550 of 15957 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Organism Source
DOID:5016
  • hepatocellular clear cell carcinoma
  • Aliases:
    • Clear cell carcinoma of the Liver cells
    • Hepatocellular carcinoma, clear cell type
Saccharomyces cerevisiae S288C
DOID:417
  • autoimmune disease
  • Aliases:
    • autoimmune hypersensitivity disease
    • hypersensitivity reaction type II disease
Saccharomyces cerevisiae S288C
DOID:0050575
  • D-2-hydroxyglutaric aciduria
Saccharomyces cerevisiae S288C
DOID:0111352
  • D-2-hydroxyglutaric aciduria 2
  • Aliases:
    • D2HGA2
Saccharomyces cerevisiae S288C
DOID:0080005
  • bone remodeling disease
Saccharomyces cerevisiae S288C
DOID:4928
  • intrahepatic cholangiocarcinoma
  • Aliases:
    • Intrahepatic bile duct carcinoma
    • peripheral Cholangiocarcinoma
Saccharomyces cerevisiae S288C
DOID:12799
  • mucopolysaccharidosis II
  • Aliases:
    • Hunter syndrome
    • Hunter's syndrome
    • MPS II - Hunter syndrome
    • Mucopolysaccharidosis, MPS-II
    • deficiency of iduronate-2-sulphatase
Homo sapiens (human)
DOID:12802
  • mucopolysaccharidosis I
  • Aliases:
    • Hurler syndrome
    • Hurler-Scheie syndrome
    • Lipochondrodystrophy
    • MPS I - Hurler syndrome
    • Mucopolysaccharidosis, MPS-I
    • Mucopolysaccharidosis, type 1
    • iduronidase deficiency disease
Homo sapiens (human)
DOID:0111389
  • mucopolysaccharidosis Ih/s
  • Aliases:
    • MPS1H/S
    • MPSIH/S
    • Mucopolysaccharidosis type 1H/S
Homo sapiens (human)
DOID:0111390
  • mucopolysaccharidosis Ih
  • Aliases:
    • Dysostosis multiplex syndrome
    • Hurler disease MPS type 1H
    • Hurler-Pfaundler syndrome
    • L-iduronidase deficiency, Hurler type
    • MPS1-H
    • Mucopolysaccharidosis type I severe form
    • dysostosis multiplex
    • gargoylism
Homo sapiens (human)
DOID:0060222
  • Scheie syndrome
  • Aliases:
    • mucopolysaccharidosis type 1S
    • mucopolysaccharidosis type IS
    • mucopolysaccharidosis type V
Homo sapiens (human)
DOID:0111994
  • immunodeficiency 45
  • Aliases:
    • IMD45
Homo sapiens (human)
DOID:2862
  • glucosephosphate dehydrogenase deficiency
  • Aliases:
    • Glucose-6-phosphate dehydrogenase deficiency
    • deficiency of G-6PD
Homo sapiens (human)
DOID:11121
  • pulpitis
  • Aliases:
    • pulp stones
Homo sapiens (human)
DOID:1884
  • viral hepatitis
  • Aliases:
    • Viral hepatitis with hepatic coma
    • animal viral hepatitis
    • human viral hepatitis
Homo sapiens (human)
DOID:11506
  • suppurative otitis media
  • Aliases:
    • Otitis media with effusion - purulent
    • Purulent otitis media
Homo sapiens (human)
DOID:0080325
  • tuberous sclerosis 2
Homo sapiens (human)
DOID:0112006
  • immunodeficiency 69
  • Aliases:
    • IMD69
Homo sapiens (human)
DOID:14176
  • selective IgG deficiency disease
  • Aliases:
    • Immunoglobin G subclass deficiency
    • Selective IgG Immunodeficiency
    • Selective Immunoglobulin G Subclass deficiency
    • Selective deficiency of IgG
    • Selective immunoglobulin G deficiency
Homo sapiens (human)
DOID:9123
  • eczema herpeticum
  • Aliases:
    • Herpes simplex dermatitis of eyelid
    • Herpes simplex eyelid dermatitis
    • Herpes simplex virus dermatitis
    • herpes simplex dermatitis
    • herpes simplex virus eyelid dermatitis
Homo sapiens (human)
DOID:0111955
  • immunodeficiency 27A
  • Aliases:
    • IMD27A
    • autosomal recessive IFNGR1 deficiency
    • autosomal recessive MSMD due to partial IFNgammaR1 deficiency
    • autosomal recessive MSMD due to partial interferon gamma receptor 1 deficiency
    • autosomal recessive immunodeficiency 27A, mycobacteriosis
    • autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency
    • autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial interferon gamma receptor 1 deficiency
Homo sapiens (human)
DOID:0111956
  • immunodeficiency 27B
  • Aliases:
    • IMD27B
    • autosomal dominant IFNGR1 deficiency
    • autosomal dominant MSMD due to partial IFNgammaR1 deficiency
    • autosomal dominant MSMD due to partial interferon gamma receptor 1 deficiency
    • autosomal dominant immunodeficiency 27B, mycobacteriosis
    • autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency
    • autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial interferon gamma receptor 1 deficiency
Homo sapiens (human)
DOID:0111995
  • immunodeficiency 28
  • Aliases:
    • IFNGR2 deficiency
    • IMD28
    • MSMD due to complete IFNgammaR2 deficiency
    • MSMD due to complete interferon gamma receptor 2 deficiency
    • Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR2 deficiency
    • Mendelian susceptibility to mycobacterial diseases due to complete interferon gamma receptor 2 deficiency
    • immunodeficiency 28, mycobacteriosis
Homo sapiens (human)
DOID:0081011
  • Bardet-Biedl syndrome 22
Homo sapiens (human)
DOID:0112352
  • spermatogenic failure 58
  • Aliases:
    • SPGF58
Homo sapiens (human)
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Last updated: December 9, 2024