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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 6501 - 6525 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:0080631
  • Elsahy-Waters syndrome
  • Aliases:
    • branchioskeletogenital syndrome
Mus musculus (house mouse)
DOID:1024
  • leprosy
Mus musculus (house mouse)
DOID:13399
  • color blindness
  • Aliases:
    • BLINDNESS COLOR
    • Colour blindness
    • Colour vision deficiency
Caenorhabditis elegans
DOID:0070453
  • xanthinuria type II
  • Aliases:
    • XAN2
Homo sapiens (human)
DOID:0110196
  • Charcot-Marie-Tooth disease type 4G
  • Aliases:
    • CMT4G
    • Charcot-Marie-Tooth neuropathy type 4G
    • HMSNR
    • autosomal recessive Charcot-Marie-Tooth disease type 4G
    • hereditary motor and sensory neuropathy Russe type
Saccharomyces cerevisiae S288C
DOID:0111801
  • syndromic microphthalmia 3
  • Aliases:
    • AEG syndrome
    • MCOPS3
    • SOX2 anophthalmia syndrome
    • anophthalmia clinical with associated anomalies
    • anophthalmia esophageal genital syndrome
    • anophthalmia microphthalmia esophageal atresia
    • anophthalmia/microphthalmia-esophageal atresia syndrome
    • microphthalmia and esophageal atresia syndrome
    • syndromic microphthalmia type 3
Homo sapiens (human)
DOID:3181
  • oligodendroglioma
  • Aliases:
    • oligodendroglial neoplasm
    • oligodendroglial tumor
Homo sapiens (human)
DOID:9206
  • Barrett's esophagus
  • Aliases:
    • Barrett esophagus
    • Barrett's esophagus with esophagitis
    • Barrett's oesophagus
    • Barrett's ulcer of esophagus
    • Barretts syndrome
    • ulcerative esophagitis
Homo sapiens (human)
DOID:234
  • colon adenocarcinoma
  • Aliases:
    • Colonic adenocarcinoma
    • adenocarcinoma of colon
Rattus norvegicus (Norway rat)
DOID:0060889
  • prune belly syndrome
  • Aliases:
    • Eagle-Barret syndrome
    • Obrisnksy syndrome
    • abdominal muscle deficiency syndrome
Caenorhabditis elegans
DOID:0060355
  • amyotrophic lateral sclerosis type 22
  • Aliases:
    • ALS 22
    • amyotrohpic lateral sclerosis 22 with or without frontotemporal dementia
    • amyotrophic lateral sclerosis 22
Homo sapiens (human)
DOID:0112319
  • Kanzaki disease
  • Aliases:
    • NAGA deficiency type 2
    • adult-onset alpha-N-acetylgalactosaminidase deficiency
    • alpha-N-acetylgalactosaminidase deficiency type 2
Caenorhabditis elegans
DOID:0081401
  • autosomal dominant distal hereditary motor neuronopathy 13
Mus musculus (house mouse)
DOID:0080345
  • blepharocheilodontic syndrome 1
Danio rerio (zebrafish)
DOID:0111344
  • myeloproliferative disorder with eosinophilia
  • Aliases:
    • chronic myeloproliferative disorder with eosinophilia
Drosophila melanogaster (fruit fly)
DOID:4479
  • pseudohypoaldosteronism
Rattus norvegicus (Norway rat)
DOID:0111386
  • inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 3
  • Aliases:
    • IBMPFD3
    • MSP3
    • multisystem proteinopathy 3
Mus musculus (house mouse)
DOID:0070303
  • multiple epiphyseal dysplasia 1
  • Aliases:
    • EDM1
    • MED1
    • multiple epiphyseal dysplasia COMP-related
    • polyepiphyseal dysplasia type 1
Rattus norvegicus (Norway rat)
DOID:0081151
  • common variable immunodeficiency 8
  • Aliases:
    • common variable immunodeficiency-8 (CVID8) with autoimmunity
Homo sapiens (human)
DOID:0111558
  • Charcot-Marie-Tooth disease type 2DD
  • Aliases:
    • ATP1A1-related CMT2
    • ATP1A1-related autosomal dominant Charcot-Marie-Tooth disease type 2
    • CMT2DD
    • Charcot-Marie-Tooth disease, axonal, type 2DD
    • Charcot-Marie-Tooth neuropathy, type 2DD
Mus musculus (house mouse)
DOID:13099
  • Moyamoya disease
  • Aliases:
    • progressive intracranial arterial occlusion
Caenorhabditis elegans
DOID:0080985
  • syndromic X-linked intellectual disorder Lujan-Fryns-type
Saccharomyces cerevisiae S288C
DOID:0111503
  • Li-Fraumeni syndrome 1
  • Aliases:
    • LFS1
Mus musculus (house mouse)
DOID:3910
  • lung adenocarcinoma
  • Aliases:
    • bronchogenic lung adenocarcinoma
    • nonsmall cell adenocarcinoma
Rattus norvegicus (Norway rat)
DOID:0070515
  • chromosome 16p11.2 deletion syndrome, 593-kb
  • Aliases:
    • Proximal 16p11.2 microdeletion syndrome
Drosophila melanogaster (fruit fly)
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Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: December 9, 2024