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 2701 - 2725 of 4621 in total
Disease ID ▲ Disease Name Gene Symbol Gene ID Organism
DOID:14159
  • obstructive hydrocephalus
Homo sapiens (human)
DOID:14174
  • central neurocytoma
  • Aliases:
    • Neurolipocytoma
Homo sapiens (human)
DOID:14175
  • von Hippel-Lindau disease
  • Aliases:
    • Hippel Lindau syndrome
    • von Hippel-Lindau syndrome
Homo sapiens (human)
DOID:14176
  • selective IgG deficiency disease
  • Aliases:
    • Immunoglobin G subclass deficiency
    • Selective IgG Immunodeficiency
    • Selective Immunoglobulin G Subclass deficiency
    • Selective deficiency of IgG
    • Selective immunoglobulin G deficiency
Homo sapiens (human)
DOID:14177
  • congenital hypogammaglobulinemia
  • Aliases:
    • Congenital hypogammaglobulinaemia
Homo sapiens (human)
DOID:14179
  • X-linked agammaglobulinemia
  • Aliases:
    • BTK deficiency
    • Bruton agammaglobulinemia tyrosine kinase deficiency
    • Bruton disease
    • Bruton's Sex-Linked Agammaglobulinemia
    • Bruton's agammaglobulinaemia
    • Bruton's type agammaglobulinemia
    • Bruton-type agammaglobulinemia
Homo sapiens (human)
DOID:14181
  • calcific tendinitis
Homo sapiens (human)
DOID:14183
  • alcoholic neuropathy
  • Aliases:
    • Alcohol-related polyneuropathy
    • Alcoholic polyneuropathy
Homo sapiens (human)
DOID:14188
  • frozen shoulder
  • Aliases:
    • Adhesive capsulitis of shoulder
    • adhesions-capsulitis,shoulder
Homo sapiens (human)
DOID:14203
  • childhood type dermatomyositis
  • Aliases:
    • Juvenile dermatomyositis
    • childhood Dermatomyositis
Homo sapiens (human)
DOID:14213
  • hypophosphatasia
  • Aliases:
    • deficiency of alkaline phosphatase
Homo sapiens (human)
DOID:14219
  • renal tubular acidosis
Homo sapiens (human)
DOID:14221
  • abdominal obesity-metabolic syndrome 1
  • Aliases:
    • dysmetabolic syndrome X
    • metabolic syndrome X
Homo sapiens (human)
DOID:14223
  • ochronosis
Homo sapiens (human)
DOID:14224
  • tracheal calcification
  • Aliases:
    • Calcification of trachea
Homo sapiens (human)
DOID:14227
  • azoospermia
Homo sapiens (human)
DOID:14228
  • oligospermia
Homo sapiens (human)
DOID:14239
  • gastrointestinal tularemia
  • Aliases:
    • Enteric tularemia
    • intestinal tularaemia
Homo sapiens (human)
DOID:14247
  • chronic purulent otitis media
  • Aliases:
    • chronic suppurative otitis media
Homo sapiens (human)
DOID:1425
  • pyoureter
  • Aliases:
    • Ureter abscess
Homo sapiens (human)
DOID:14250
  • Down syndrome
  • Aliases:
    • Complete trisomy 21 syndrome
    • Down's syndrome
    • Down's syndrome - trisomy 21
    • Downs syndrome
    • G Trisomy
    • trisomy 21 syndrome
Homo sapiens (human)
DOID:14256
  • adult-onset Still's disease
  • Aliases:
    • adult onset Still's disease
    • adult-onset Still disease
Homo sapiens (human)
DOID:14261
  • fragile X syndrome
  • Aliases:
    • FRAGILE X MENTAL RETARDATION SYNDROME
    • MARKER X SYNDROME
    • MARTIN-BELL SYNDROME
Homo sapiens (human)
DOID:14262
  • oral candidiasis
  • Aliases:
    • Candidiasis of mouth
    • Oral moniliasis
    • Thrush, oral
    • thrush
Homo sapiens (human)
DOID:14264
  • benign neonatal seizures
  • Aliases:
    • benign familial neonatal seizures
    • benign neonatal convulsions
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