GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB), DisGeNET, and Alliance of Genome Resources is integrated into one list.

Source Last Updated
Alliance of Genome Resources July 29, 2024
DisGeNET July 29, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 4001 - 4025 of 4621 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲
DOID:13608
  • biliary atresia
  • Aliases:
    • Atresia of bile duct
    • Congenital biliary atresia
    • biliary atresia, congenital
Homo sapiens (human)
DOID:5348
  • adult endodermal sinus tumor
  • Aliases:
    • adult Yolk Sac neoplasm
    • adult endodermal sinus neoplasm
Homo sapiens (human)
DOID:0060705
  • X-linked lymphoproliferative syndrome 1
  • Aliases:
    • XLP1
Homo sapiens (human)
DOID:10609
  • rickets
  • Aliases:
    • active rickets
Homo sapiens (human)
DOID:7689
  • leptomeninges sarcoma
  • Aliases:
    • Leptomeningeal sarcoma
    • sarcoma of Leptomeninges
Homo sapiens (human)
DOID:4535
  • hypotrichosis
Homo sapiens (human)
DOID:1947
  • trichomoniasis
Homo sapiens (human)
DOID:2510
  • Kluver-Bucy syndrome
  • Aliases:
    • Klver-Bucy syndrome
Homo sapiens (human)
DOID:0111060
  • Ambras type hypertrichosis universalis congenita
  • Aliases:
    • Ambras syndrome
    • HTC1
Homo sapiens (human)
DOID:6228
  • peritoneal serous papillary adenocarcinoma
  • Aliases:
    • primary serous papillary carcinoma of peritoneum
Homo sapiens (human)
DOID:3012
  • Li-Fraumeni syndrome
  • Aliases:
    • LFS
    • Li-Fraumeni Familiar cancer Susceptibility syndrome
    • SBLA syndrome
    • sarcoma, breast, leukaemia and adrenal gland syndrome
Homo sapiens (human)
DOID:0060785
  • adult-onset autosomal dominant demyelinating leukodystrophy
  • Aliases:
    • ADLD
    • adult-onset autosomal dominant leukodystrophy
    • autosomal-dominant or late-onset type Pelizaeus-Merzbacher disease
Homo sapiens (human)
DOID:4961
  • bone marrow disease
  • Aliases:
    • bone marrow disorder
Homo sapiens (human)
DOID:4195
  • hyperglycemia
Homo sapiens (human)
DOID:9540
  • vascular skin disease
Homo sapiens (human)
DOID:9741
  • biliary tract disease
Homo sapiens (human)
DOID:0060222
  • Scheie syndrome
  • Aliases:
    • mucopolysaccharidosis type 1S
    • mucopolysaccharidosis type IS
    • mucopolysaccharidosis type V
Homo sapiens (human)
DOID:10907
  • microcephaly
  • Aliases:
    • Microcephalus
    • microencephaly
Homo sapiens (human)
DOID:1596
  • depressive disorder
  • Aliases:
    • mental depression
Homo sapiens (human)
DOID:2583
  • agammaglobulinemia
  • Aliases:
    • IGHM
    • hypogammaglobulinemia
    • mu heavy chain deficiency
Homo sapiens (human)
DOID:0110262
  • cataract 45
  • Aliases:
    • CTRCT45
Homo sapiens (human)
DOID:8506
  • bullous pemphigoid
Homo sapiens (human)
DOID:13206
  • nodular prostate
Homo sapiens (human)
DOID:12179
  • tinea corporis
  • Aliases:
    • Dermatophytosis of the trunk
    • dermatophytosis of the body
Homo sapiens (human)
DOID:0110268
  • cataract 22 multiple types
  • Aliases:
    • CTRCT22
Homo sapiens (human)

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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: August 19, 2024