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 July 29, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 6551 - 6575 of 7942 in total
Disease ID Disease Name ▼ Gene Symbol Gene ID Organism
DOID:0111246
  • amyotrophic lateral sclerosis-parkinsonism/dementia complex 1
  • Aliases:
    • ALS-PDC
    • Amyotrophic lateral sclerosis-parkinsonism-dementia of Guam syndrome
    • Guam disease
    • Lytico-Bodig disease
    • PDALS
    • amyotrophic lateral sclerosis-parkinsonism/dementia complex of Guam
    • parkinsonism-dementia-ALS complex
Homo sapiens (human)
DOID:332
  • amyotrophic lateral sclerosis
  • Aliases:
    • ALS
    • Lou Gehrig's disease
    • motor neuron disease, bulbar
Caenorhabditis elegans
DOID:332
  • amyotrophic lateral sclerosis
  • Aliases:
    • ALS
    • Lou Gehrig's disease
    • motor neuron disease, bulbar
Mus musculus (house mouse)
DOID:332
  • amyotrophic lateral sclerosis
  • Aliases:
    • ALS
    • Lou Gehrig's disease
    • motor neuron disease, bulbar
Rattus norvegicus (Norway rat)
DOID:332
  • amyotrophic lateral sclerosis
  • Aliases:
    • ALS
    • Lou Gehrig's disease
    • motor neuron disease, bulbar
Danio rerio (zebrafish)
DOID:332
  • amyotrophic lateral sclerosis
  • Aliases:
    • ALS
    • Lou Gehrig's disease
    • motor neuron disease, bulbar
Drosophila melanogaster (fruit fly)
DOID:332
  • amyotrophic lateral sclerosis
  • Aliases:
    • ALS
    • Lou Gehrig's disease
    • motor neuron disease, bulbar
Homo sapiens (human)
DOID:0060198
  • amyotrophic lateral sclerosis type 6
  • Aliases:
    • ALS6
    • amyotrophic lateral sclerosis 6, with or without frontotemporal dementia
    • autosomal recessive amyotrophic lateral sclerosis 6
Homo sapiens (human)
DOID:0060196
  • amyotrophic lateral sclerosis type 4
  • Aliases:
    • ALS 4
    • amyotrophic lateral sclerosis 4
    • amyotrophic lateral sclerosis 4, juvenile
    • dHMN with upper motor neuron signs
    • distal hereditary motor neuropathy with pyramidal features
    • distal hereditary motor neuropathy with upper motor neuron signs
Homo sapiens (human)
DOID:0060194
  • amyotrophic lateral sclerosis type 2
  • Aliases:
    • ALS2
    • amyotrophic lateral sclerosis 2
    • amyotrophic lateral sclerosis 2, juvenile
Homo sapiens (human)
DOID:0060202
  • amyotrophic lateral sclerosis type 11
  • Aliases:
    • ALS11
    • amyotrophic lateral sclerosis 11
Homo sapiens (human)
DOID:0060202
  • amyotrophic lateral sclerosis type 11
  • Aliases:
    • ALS11
    • amyotrophic lateral sclerosis 11
Drosophila melanogaster (fruit fly)
DOID:0060202
  • amyotrophic lateral sclerosis type 11
  • Aliases:
    • ALS11
    • amyotrophic lateral sclerosis 11
Saccharomyces cerevisiae S288C
DOID:0060193
  • amyotrophic lateral sclerosis type 1
  • Aliases:
    • ALS1
    • amyotrophic lateral sclerosis 1
Homo sapiens (human)
DOID:9120
  • amyloidosis
  • Aliases:
    • amyloid disease
Mus musculus (house mouse)
DOID:9120
  • amyloidosis
  • Aliases:
    • amyloid disease
Rattus norvegicus (Norway rat)
DOID:9120
  • amyloidosis
  • Aliases:
    • amyloid disease
Homo sapiens (human)
DOID:4932
  • ampulla of Vater carcinoma
  • Aliases:
    • ampulla of vater cancer
    • ampullary carcinoma
    • carcinoma of ampulla of vater
Homo sapiens (human)
DOID:10022
  • ampulla of Vater benign neoplasm
  • Aliases:
    • tumor of the ampulla of Vater
Homo sapiens (human)
DOID:3502
  • ampulla of Vater adenocarcinoma
  • Aliases:
    • ampullary adenocarcinoma
Homo sapiens (human)
DOID:670
  • amphetamine abuse
Rattus norvegicus (Norway rat)
DOID:670
  • amphetamine abuse
Homo sapiens (human)
DOID:670
  • amphetamine abuse
Mus musculus (house mouse)
DOID:10914
  • amnestic disorder
  • Aliases:
    • Amnestic syndrome
    • Korsakoff's psychosis or syndrome
    • amnesia
Homo sapiens (human)
DOID:9252
  • amino acid metabolic disorder
  • Aliases:
    • inborn errors of amino acid metabolism
Homo sapiens (human)

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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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