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 1751 - 1775 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲
DOID:1498
  • cholera
  • Aliases:
    • Cholera - Vibrio cholerae
    • Cholera due to Vibrio cholerae
    • Vibrio cholerae
Homo sapiens (human)
DOID:10241
  • thalassemia
  • Aliases:
    • Sickle-cell thalassemia with crisis
    • Sickle-cell thalassemia without crisis
    • thalassemia Hb-S disease with crisis
    • thalassemia Hb-S disease without crisis
Homo sapiens (human)
DOID:13099
  • Moyamoya disease
  • Aliases:
    • progressive intracranial arterial occlusion
Homo sapiens (human)
DOID:5032
  • pineal gland cancer
  • Aliases:
    • Pineocytic tumor
    • malignant Pineal Region tumor
    • malignant tumor of pineal gland
    • neoplasm of pineal gland
    • neoplasm of the Pineal Region
    • pineal body neoplasm
    • tumor of the pineal region
Homo sapiens (human)
DOID:3168
  • squamous cell neoplasm
  • Aliases:
    • Epidermoid cell tumor
    • squamous cell tumor
Homo sapiens (human)
DOID:0080128
  • mitochondrial DNA depletion syndrome 9
  • Aliases:
    • fatal infantile lactic acidosis
Homo sapiens (human)
DOID:0110637
  • muscular dystrophy-dystroglycanopathy type B6
  • Aliases:
    • MDC1D
    • MDDGB6
    • congenital muscular dystrophy LARGE-related
    • congenital muscular dystrophy type 1D
    • muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 6
    • muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B, 6
Homo sapiens (human)
DOID:0110774
  • hereditary spastic paraplegia 23
  • Aliases:
    • Lison syndrome
    • SPG23
    • Spastic paraparesis-vitiligo-premature graying-characteristic facies syndrome
    • spastic paraplegia 23
    • spastic paraplegia with pigmentary abnormalities
Homo sapiens (human)
DOID:0070219
  • familial hyperinsulinemic hypoglycemia 1
  • Aliases:
    • HHF1
Homo sapiens (human)
DOID:5518
  • penis squamous cell carcinoma
  • Aliases:
    • Epidermoid cell carcinoma of penis
Homo sapiens (human)
DOID:9835
  • refractive error
Homo sapiens (human)
DOID:0050912
  • colon adenoma
Homo sapiens (human)
DOID:7474
  • malignant pleural mesothelioma
  • Aliases:
    • malignant mesothelioma of pleura
Homo sapiens (human)
DOID:2340
  • craniosynostosis
  • Aliases:
    • Premature closure of cranial sutures
Homo sapiens (human)
DOID:345
  • uterine disease
Homo sapiens (human)
DOID:5166
  • endometrial stromal tumor
  • Aliases:
    • endometrial Stromal neoplasm
Homo sapiens (human)
DOID:3304
  • germinoma
Homo sapiens (human)
DOID:0060232
  • branchiootic syndrome
  • Aliases:
    • BO syndrome
    • BOR
    • branchiootic dysplasia
Homo sapiens (human)
DOID:11161
  • neonatal respiratory failure
  • Aliases:
    • respiratory failure of newborn
Homo sapiens (human)
DOID:11603
  • infant gynecomastia
  • Aliases:
    • Neonatal gynaecomastia
    • breast engorgement in newborn
Homo sapiens (human)
DOID:7566
  • eccrine porocarcinoma
  • Aliases:
    • Eccrine porocarcinoma of skin
    • Porocarcinoma
    • malignant Eccrine Poroma
Homo sapiens (human)
DOID:0050851
  • glomerulosclerosis
Homo sapiens (human)
DOID:0110302
  • obsolete autosomal dominant limb-girdle muscular dystrophy type 1C
Homo sapiens (human)
DOID:4189
  • mutism
Homo sapiens (human)
DOID:5614
  • eye disease
Homo sapiens (human)

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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