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 7376 - 7400 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:1962
  • fallopian tube disease
Homo sapiens (human)
DOID:0110530
  • autosomal recessive nonsyndromic deafness 84B
  • Aliases:
    • DFNB84B
    • autosomal recessive deafness 84B
Mus musculus (house mouse)
DOID:2316
  • brain ischemia
  • Aliases:
    • Ischaemic encephalopathy
    • Ischemic encephalopathy
    • cerebral ischemia
Drosophila melanogaster (fruit fly)
DOID:0112001
  • immunodeficiency 50
  • Aliases:
    • CID due to Moesin deficiency
    • IMD50
    • MSN-related combined immunodeficiency
    • X-linked Moesin-associated immunodeficiency
    • combined immunodeficiency due to Moesin deficiency
    • immunodeficiency 50 X linked recessive
Mus musculus (house mouse)
DOID:0070352
  • stress-induced childhood-onset neurodegeneration with variable ataxia and seizures
  • Aliases:
    • CONDSIAS
Caenorhabditis elegans
DOID:3659
  • sialuria
Saccharomyces cerevisiae S288C
DOID:2871
  • endometrial carcinoma
  • Aliases:
    • carcinoma of the Endometrium
    • endometrioid carcinoma
    • endometrioid carcinoma of female Reproductive system
Danio rerio (zebrafish)
DOID:0080600
  • COVID-19
  • Aliases:
    • 2019 Novel Coronavirus (2019-nCoV)
    • 2019-nCoV infection
    • COVID19
    • SARS-CoV-2 infection
    • Wuhan coronavirus infection
    • Wuhan seafood market pneumonia virus infection
Danio rerio (zebrafish)
DOID:14400
  • capillary leak syndrome
Mus musculus (house mouse)
DOID:1307
  • dementia
Mus musculus (house mouse)
DOID:769
  • neuroblastoma
Homo sapiens (human)
DOID:2367
  • neuroaxonal dystrophy
Rattus norvegicus (Norway rat)
DOID:0111030
  • hemochromatosis type 3
  • Aliases:
    • HFE3
    • TFR2-related hemochromatosis
    • hemochromatosis due to defect in transferrin receptor 2
Rattus norvegicus (Norway rat)
DOID:0070134
  • autosomal recessive cutis laxa type IIA
  • Aliases:
    • ARCL2A
Homo sapiens (human)
DOID:0112337
  • spermatogenic failure 55
  • Aliases:
    • SPGF55
Mus musculus (house mouse)
DOID:0080517
  • Meier-Gorlin syndrome 6
Homo sapiens (human)
DOID:0050752
  • amyotrophic lateral sclerosis type 8
  • Aliases:
    • ALS8
    • amyotrophic lateral sclerosis 8
Homo sapiens (human)
DOID:1572
  • normal pressure hydrocephalus
  • Aliases:
    • Low pressure hydrocephalus
Mus musculus (house mouse)
DOID:670
  • amphetamine abuse
Caenorhabditis elegans
DOID:0112105
  • X-linked parkinsonism-spasticity syndrome
  • Aliases:
    • X-linked Parkinsonism with spasticity
    • XPDS
Homo sapiens (human)
DOID:0070339
  • cerebellar hyplasia/atrophy, epilepsy, and global developmental delay
Homo sapiens (human)
DOID:0110210
  • Charcot-Marie-Tooth disease X-linked recessive 5
  • Aliases:
    • CMT5X
    • CMTX5
    • Charcot-Marie-Tooth neuropathy X-linked recessive 5
    • Rosenberg-Chutorian syndrome
    • X-linked Charcot-Marie-Tooth disease type 5
    • optic atrophy, polyneuropathy, and deafness
Mus musculus (house mouse)
DOID:13366
  • Stiff-Person syndrome
  • Aliases:
    • Stiff-man syndrome
    • stiff man syndrome
Mus musculus (house mouse)
DOID:0080444
  • developmental and epileptic encephalopathy 27
  • Aliases:
    • DEE27
    • early infantile epileptic encephalopathy 27
Homo sapiens (human)
DOID:693
  • dental enamel hypoplasia
  • Aliases:
    • enamel hypoplasia
Danio rerio (zebrafish)

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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