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 5601 - 5625 of 7942 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism
DOID:5812
  • MHC class II deficiency
  • Aliases:
    • BLSII
    • SCID due to absent class II HLA antigens
    • bare lymphocyte syndrome type II
Homo sapiens (human)
DOID:5810
  • adenosine deaminase deficiency
  • Aliases:
    • ADA
Homo sapiens (human)
DOID:0050540
  • Charcot-Marie-Tooth disease type 3
  • Aliases:
    • DEJERINE-SOTTAS NEUROPATHY
    • DEJERINE-SOTTAS SYNDROME
Homo sapiens (human)
DOID:8634
  • prostate carcinoma in situ
  • Aliases:
    • PIN III
    • carcinoma in situ of prostate
    • grade III PIN
Homo sapiens (human)
DOID:7079
  • adult cystic teratoma
Homo sapiens (human)
DOID:2660
  • cystic teratoma
Homo sapiens (human)
DOID:5565
  • adult teratoma
Homo sapiens (human)
DOID:0050486
  • exanthem
Homo sapiens (human)
DOID:0111169
  • subcortical band heterotopia
  • Aliases:
    • HeCo
    • band heterotopia
    • double cortex syndrome
    • heterotopic cortex
    • subcortical laminar heterotopia
Homo sapiens (human)
DOID:450
  • myotonic disease
Homo sapiens (human)
DOID:13619
  • extrahepatic cholestasis
  • Aliases:
    • extrahepatic biliary Stasis
    • extrahepatic obstructive biliary disease
Homo sapiens (human)
DOID:0060700
  • familial hypocalciuric hypercalcemia 1
  • Aliases:
    • FHH type 1
    • HHC1
    • familial benign hypercalcemia 1
    • familial hypocalciuric hypercalcemia type I
    • hypocalciuric hypercalcemia type I
Homo sapiens (human)
DOID:5690
  • well-differentiated liposarcoma
  • Aliases:
    • atypical lipomatous tumor
Homo sapiens (human)
DOID:5704
  • sclerosing liposarcoma
Homo sapiens (human)
DOID:8233
  • inflammatory liposarcoma
Homo sapiens (human)
DOID:0060402
  • chromosome 17p13.1 deletion syndrome
Homo sapiens (human)
DOID:74
  • hematopoietic system disease
  • Aliases:
    • Blood disease
    • Blood dyscrasia
    • DISEASE OF THE BLOOD AND BLOOD-FORMING ORGANS
    • Hematological disease
    • blood disorder
    • disease of haematopoietic system
    • disease of hematopoietic system
    • haematopoietic system disease
Homo sapiens (human)
DOID:674
  • cleft palate
  • Aliases:
    • Palatoschisis
Homo sapiens (human)
DOID:0110213
  • isolated cleft palate
Homo sapiens (human)
DOID:0050453
  • lissencephaly
Homo sapiens (human)
DOID:2717
  • Bloom syndrome
  • Aliases:
    • Bloom-Torre-Machacek syndrome
    • Congenital Telangiectatic Erythema syndrome
Homo sapiens (human)
DOID:0111344
  • myeloproliferative disorder with eosinophilia
  • Aliases:
    • chronic myeloproliferative disorder with eosinophilia
Homo sapiens (human)
DOID:0110915
  • childhood hypophosphatasia
Homo sapiens (human)
DOID:0050763
  • ARC syndrome
  • Aliases:
    • ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS
    • Arthrogryposis, renal dysfunction and cholestasis (ARC) syndrome
    • Arthrogryposis-renal dysfunction-cholestasis
Homo sapiens (human)
DOID:0111353
  • arthrogryposis, renal dysfunction, and cholestasis 1
  • Aliases:
    • ARCS1
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