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 1776 - 1800 of 4621 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼
DOID:5574
  • VIPoma
  • Aliases:
    • VIP- Secreting tumor
    • Vasoactive intestinal peptide-secreting tumor
    • Vipoma, malignant
    • malignant vasoactive intestinal peptide-secreting tumor
Homo sapiens (human)
DOID:2846
  • bruxism
  • Aliases:
    • Bruxism - teeth grinding
    • Grinding teeth
    • Teeth grinding
    • sleep related bruxism
Homo sapiens (human)
DOID:0050855
  • renal fibrosis
Homo sapiens (human)
DOID:0110131
  • Bardet-Biedl syndrome 9
  • Aliases:
    • BBS9
Homo sapiens (human)
DOID:0112333
  • pontocerebellar hypoplasia type 16
  • Aliases:
    • PCH16
Homo sapiens (human)
DOID:14080
  • glucocorticoid-remediable aldosteronism
  • Aliases:
    • GRA
    • GRS
    • familial hyperaldosteronism type I
    • glucocorticoid-suppressible hyperaldosteronism
Homo sapiens (human)
DOID:0060573
  • von Willebrand's disease 1
  • Aliases:
    • VWD type 1
    • VWD1
    • von Willebrand disease type 1
    • von Willebrand disease type I
Homo sapiens (human)
DOID:0070395
  • developmental and epileptic encephalopathy 110
  • Aliases:
    • DEE110
    • early infantile epileptic encephalopathy 110
Homo sapiens (human)
DOID:0110791
  • hereditary spastic paraplegia 3A
  • Aliases:
    • FSP1
    • SPG3A
    • autosomal dominant familial spastic paraplegia 1
    • autosomal dominant spastic paraplegia 3
    • autosomal dominant spastic paraplegia type 3
    • strumpell disease
Homo sapiens (human)
DOID:0060567
  • erythema elevatum diutinum
Homo sapiens (human)
DOID:0112319
  • Kanzaki disease
  • Aliases:
    • NAGA deficiency type 2
    • adult-onset alpha-N-acetylgalactosaminidase deficiency
    • alpha-N-acetylgalactosaminidase deficiency type 2
Homo sapiens (human)
DOID:9952
  • acute lymphoblastic leukemia
  • Aliases:
    • ALL
    • acute lymphoblastic leukaemia
    • acute lymphocytic leukaemia
    • precursor lymphoblastic lymphoma/leukemia
Homo sapiens (human)
DOID:479
  • angiokeratoma
  • Aliases:
    • Angiokeratoma of skin
    • Cutaneous Angiokeratoma
    • skin angiokeratoma
Homo sapiens (human)
DOID:0070219
  • familial hyperinsulinemic hypoglycemia 1
  • Aliases:
    • HHF1
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:0111626
  • D-glyceric aciduria
  • Aliases:
    • D-glycerate kinase deficiency
    • D-glyceric acidemia
    • D-glycericacidemia
    • deficiency of glycerate kinase
    • non ketotic hyperglycinemia syndrome
Homo sapiens (human)
DOID:11427
  • endosalpingiosis
Homo sapiens (human)
DOID:0090077
  • hypogonadotropic hypogonadism 4 with or without anosmia
Homo sapiens (human)
DOID:1673
  • pneumothorax
Homo sapiens (human)
DOID:11269
  • chronic apical periodontitis
Homo sapiens (human)
DOID:0090032
  • Silverman-Handmaker type dyssegmental dysplasia
Homo sapiens (human)
DOID:3308
  • embryonal carcinoma
  • Aliases:
    • primary extragonadal embryonal carcinoma
Homo sapiens (human)
DOID:0110546
  • autosomal dominant nonsyndromic deafness 15
  • Aliases:
    • DFNA15
    • autosomal dominant deafness 15
Homo sapiens (human)
DOID:0111330
  • combined saposin deficiency
  • Aliases:
    • PSAPD
    • combined SAP deficiency
    • encephalopathy due to prosaposin deficiency
Homo sapiens (human)
DOID:0080288
  • spinocerebellar ataxia 46
Homo sapiens (human)

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Last updated: August 19, 2024