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 776 - 800 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲ Source
DOID:10908
  • hydrocephalus
  • Aliases:
    • hydrocephalus, X-linked
    • hydrocephalus, nonsyndromic, autosomal recessive
Caenorhabditis elegans
DOID:8893
  • psoriasis
Caenorhabditis elegans
DOID:820
  • myocarditis
  • Aliases:
    • Myocardial inflammation
Caenorhabditis elegans
DOID:1324
  • lung cancer
Caenorhabditis elegans
DOID:2986
  • IgA glomerulonephritis
  • Aliases:
    • Berger's IgA or IgG nephropathy
    • Focal Glomerulonephritis
    • IgA nephropathy
    • primary IgA nephropathy
    • segmental glomerulonephritis
Caenorhabditis elegans
DOID:13533
  • osteopetrosis
  • Aliases:
    • Albers-Schonberg disease
    • marble bone
Caenorhabditis elegans
DOID:0050127
  • sinusitis
Caenorhabditis elegans
DOID:9206
  • Barrett's esophagus
  • Aliases:
    • Barrett esophagus
    • Barrett's esophagus with esophagitis
    • Barrett's oesophagus
    • Barrett's ulcer of esophagus
    • Barretts syndrome
    • ulcerative esophagitis
Caenorhabditis elegans
DOID:1148
  • polydactyly
  • Aliases:
    • postaxial polydactyly
Caenorhabditis elegans
DOID:0070232
  • benign recurrent intrahepatic cholestasis 2
  • Aliases:
    • BRIC type 2
    • BRIC2
Caenorhabditis elegans
DOID:0081097
  • Rafiq syndrome
  • Aliases:
    • MENTAL RETARDATION, AUTOSOMAL RECESSIVE 15
Caenorhabditis elegans
DOID:0070068
  • autosomal dominant intellectual developmental disorder 38
  • Aliases:
    • MRD38
    • PRELDS
    • autosomal dominant mental retardation 38
    • autosomal dominant non-syndromic intellectual disability 38
    • psychomotor retardation, epilepsy, and language disability syndrome
Caenorhabditis elegans
DOID:0080176
  • meningococcal meningitis
Caenorhabditis elegans
DOID:2377
  • multiple sclerosis
  • Aliases:
    • Generalized multiple sclerosis
    • insular sclerosis
Caenorhabditis elegans
DOID:0080797
  • nasal type extranodal NK/T-cell lymphoma
Caenorhabditis elegans
DOID:0080561
  • congenital disorder of glycosylation Ii
  • Aliases:
    • congenital disorder of glycosylation 1i
Caenorhabditis elegans
DOID:0070422
  • syndromic X-linked intellectual disability Pilorge type
  • Aliases:
    • MRXSP
Caenorhabditis elegans
DOID:0070223
  • progressive familial intrahepatic cholestasis 3
  • Aliases:
    • MDR3 deficiency
    • PFIC3
    • progressive familial intrahepatic cholestasis with elevated serum gama-glutamyltransferase
Caenorhabditis elegans
DOID:3892
  • insulinoma
  • Aliases:
    • Insulin-Producing tumor of Islet cells
    • Islet cell adenoma
Caenorhabditis elegans
DOID:0111607
  • distal arthrogryposis type 3
  • Aliases:
    • DA3
    • Gordon syndrome
    • camptodactyly-cleft palate-clubfoot syndrome
    • distal arthrogryposis multiplex congenita type IIA
Caenorhabditis elegans
DOID:0111526
  • Mullerian aplasia and hyperandrogenism
  • Aliases:
    • Mullerian duct failure and hyperandrogenism
    • WNT4 deficiency
Caenorhabditis elegans
DOID:0050458
  • juvenile myelomonocytic leukemia
Caenorhabditis elegans
DOID:0110034
  • X-linked Alport syndrome
  • Aliases:
    • nephropathy and deafness, X-linked
Caenorhabditis elegans
DOID:9470
  • bacterial meningitis
Caenorhabditis elegans
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
Caenorhabditis elegans

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Last updated: December 9, 2024