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 3626 - 3650 of 4621 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Organism
DOID:0050888
  • syndromic intellectual disability
Homo sapiens (human)
DOID:4372
  • intracranial embolism
  • Aliases:
    • Cerebral embolism with cerebral infarction
    • cerebral embolism
Homo sapiens (human)
DOID:0111156
  • spermatogenic failure 9
  • Aliases:
    • globozoospermia
    • male infertility due to round-headed spermatozoa
Homo sapiens (human)
DOID:0070432
  • hyperphosphatasia with impaired intellectual development syndrome 5
  • Aliases:
    • GPIBD11
    • HPMRS5
    • glycosylphosphatidylinositol biosynthesis defect 11
    • hyperphosphatasia with mental retardation syndrome 5
Homo sapiens (human)
DOID:0060227
  • Adams-Oliver syndrome
  • Aliases:
    • Adams Oliver syndrome
Homo sapiens (human)
DOID:0050441
  • mucosulfatidosis
  • Aliases:
    • Sulfatidosis, Juvenile, Austin Type
    • multiple sulfatase deficiency disease
Homo sapiens (human)
DOID:13272
  • Klebsiella pneumonia
  • Aliases:
    • Pneumonia due to Klebsiella pneumoniae
    • Pneumonia due to Klebsiella pneumoniae (disorder)
Homo sapiens (human)
DOID:7371
  • superficial urinary bladder cancer
  • Aliases:
    • Superficial urinary bladder carcinoma
Homo sapiens (human)
DOID:11758
  • iron deficiency anemia
Homo sapiens (human)
DOID:0070004
  • myeloid neoplasm
Homo sapiens (human)
DOID:7941
  • Barrett's adenocarcinoma
  • Aliases:
    • Barrett adenocarcinoma
    • adenocarcinoma Arising in Barrett's Mucosa
Homo sapiens (human)
DOID:13129
  • severe pre-eclampsia
  • Aliases:
    • Severe pre-eclampsia, with delivery
    • antepartum severe pre-eclampsia
    • postpartum severe pre-eclampsia
    • severe preeclampsia
Homo sapiens (human)
DOID:14701
  • propionic acidemia
  • Aliases:
    • GLYCINEMIA, KETOTIC
    • KETOTIC HYPERGLYCINEMIA
    • ketotic II glycinemia
    • ketotic glycinemia
    • propionic aciduria
    • propionyl-CoA carboxylase deficiency
Homo sapiens (human)
DOID:0110406
  • retinitis pigmentosa 30
  • Aliases:
    • RP30
Homo sapiens (human)
DOID:0080797
  • nasal type extranodal NK/T-cell lymphoma
Homo sapiens (human)
DOID:10590
  • mild pre-eclampsia
Homo sapiens (human)
DOID:0050967
  • spinocerebellar ataxia type 17
Homo sapiens (human)
DOID:0050850
  • diabetic encephalopathy
Homo sapiens (human)
DOID:12803
  • Sly syndrome
  • Aliases:
    • MPS VII - Sly syndrome
    • beta-glucuronidase deficiency
    • deficiency of beta-glucuronidase
    • mucopolysaccharidosis VII
Homo sapiens (human)
DOID:0050579
  • glycogen storage disease XV
  • Aliases:
    • Glycogen storage disease 15
    • Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency
    • glycogen storage disease type XV
Homo sapiens (human)
DOID:0111233
  • congenital muscular dystrophy-dystroglycanopathy A14
  • Aliases:
    • MDDGA14
    • Walker-Warburg syndrome or muscle-eye-brain disease GMPPB-related
    • congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A14
Homo sapiens (human)
DOID:0112377
  • muscular dystrophy-dystroglycanopathy type B14
  • Aliases:
    • MDDGB14
    • congenital muscular dystrophy GMPPB-related
Homo sapiens (human)
DOID:0050602
  • triple-A syndrome
  • Aliases:
    • AAAS
    • Achalasia-Addisonianism-Alacrimia syndrome
    • Allgrove Syndrome
Homo sapiens (human)
DOID:0112321
  • alacrima, achalasia, and impaired intellectual development syndrome
  • Aliases:
    • AAMR
    • alacrima, achalasia, and mental retardation syndrome
Homo sapiens (human)
DOID:0080555
  • congenital disorder of glycosylation Ic
  • Aliases:
    • congenital disorder of glycosylation 1c
Homo sapiens (human)

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Last updated: August 19, 2024