GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB) and Alliance of Genome Resources is integrated into one list.

Source Last Updated
Alliance of Genome Resources October 9, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 826 - 850 of 4649 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source ▼
DOID:3321
  • GM2 gangliosidosis
  • Aliases:
    • gangliosidosis GM2
Homo sapiens (human)
DOID:332
  • amyotrophic lateral sclerosis
  • Aliases:
    • ALS
    • Lou Gehrig's disease
    • motor neuron disease, bulbar
Homo sapiens (human)
DOID:3319
  • lymphangioleiomyomatosis
  • Aliases:
    • lung lymphangioleiomyomatosis
    • lymphangiomyomatosis
    • pulmonary lymphangioleiomyomatosis
Homo sapiens (human)
DOID:3317
  • hepatic angiomyolipoma
Homo sapiens (human)
DOID:3314
  • angiomyolipoma
Homo sapiens (human)
DOID:3312
  • bipolar disorder
  • Aliases:
    • Manic Bipolar Affective disorder
    • Manic Depressive disorder
    • Manic bipolar I disorder
    • bipolar depression
    • bipolar disorder manic phase
    • manic depression
    • manic disorder
    • mixed bipolar disorder
Homo sapiens (human)
DOID:3310
  • atopic dermatitis
  • Aliases:
    • Atopic neurodermatitis
    • Besnier's prurigo
    • allergic dermatitis
    • atopic eczema
Homo sapiens (human)
DOID:331
  • central nervous system disease
Homo sapiens (human)
DOID:3308
  • embryonal carcinoma
  • Aliases:
    • primary extragonadal embryonal carcinoma
Homo sapiens (human)
DOID:3307
  • teratoma
Homo sapiens (human)
DOID:3305
  • teratocarcinoma
  • Aliases:
    • mixed Embryonal carcinoma and teratoma
Homo sapiens (human)
DOID:3304
  • germinoma
Homo sapiens (human)
DOID:3275
  • thymoma
Homo sapiens (human)
DOID:3265
  • chronic granulomatous disease
  • Aliases:
    • Bridges-Good syndrome
    • CGD
    • Congenital dysphagocytosis
    • Quie syndrome
Homo sapiens (human)
DOID:3263
  • piebaldism
  • Aliases:
    • PIEBALD TRAIT
    • Partial albinism
Homo sapiens (human)
DOID:3261
  • hyper IgE recurrent infection syndrome 1
  • Aliases:
    • Job syndrome
    • Job's syndrome
    • hyperimmunoglobulin E syndrome
Homo sapiens (human)
DOID:326
  • ischemia
Homo sapiens (human)
DOID:3247
  • rhabdomyosarcoma
Homo sapiens (human)
DOID:3234
  • central nervous system lymphoma
  • Aliases:
    • Microglioma
    • primary CNS lymphoma
Homo sapiens (human)
DOID:3227
  • tracheal stenosis
  • Aliases:
    • Stenosis of trachea
Homo sapiens (human)
DOID:322
  • myelitis
Homo sapiens (human)
DOID:3213
  • demyelinating disease
  • Aliases:
    • demyelinating disorder
Homo sapiens (human)
DOID:3211
  • lysosomal storage disease
  • Aliases:
    • disorder of lysosomal enzyme
    • inborn lysosomal enzyme disorder
    • lysosomal storage metabolism disorder
Homo sapiens (human)
DOID:3210
  • Pelizaeus-Merzbacher disease
  • Aliases:
    • HLD1
    • Leukodystrophy, sudanophilic
    • PMD
    • Pelizaeus Merzbacher brain sclerosis
    • Pelizaeus-Merzbacher brain sclerosis
    • diffuse familial brain sclerosis
    • hypomyelinating leukodystrophy 1
    • sudanophilic leukodystrophy, Paelizeus-Merzbacher type
Homo sapiens (human)
DOID:321
  • tropical spastic paraparesis
  • Aliases:
    • HTLV-associated myelopathy
    • Tropical spastic paralysis
    • Tropical spastic paraplegia
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: December 9, 2024