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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 9176 - 9200 of 15957 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Organism Source
DOID:643
  • progressive multifocal leukoencephalopathy
Homo sapiens (human)
DOID:0110149
  • Charcot-Marie-Tooth disease type 1F
  • Aliases:
    • CMT1F
    • Charcot-Marie-Tooth neuropathy type 1F
Homo sapiens (human)
DOID:0080294
  • Charcot-Marie-Tooth disease dominant intermediate G
Homo sapiens (human)
DOID:0081378
  • amyotrophic lateral sclerosis type 24
Homo sapiens (human)
DOID:0110092
  • short-rib thoracic dysplasia 6 with or without polydactyly
  • Aliases:
    • Majewski syndrome
    • SRPS2A
    • SRTD6
    • polydactyly with neonatal chondrodystrophy, type II
    • short rib-polydactyly syndrome type IIA
Homo sapiens (human)
DOID:0110326
  • hypertrophic cardiomyopathy 20
  • Aliases:
    • CMH20
    • cardiomyopathy familial hypertrophic 20
Homo sapiens (human)
DOID:0110424
  • dilated cardiomyopathy 1CC
  • Aliases:
    • CMD1CC
Homo sapiens (human)
DOID:0111253
  • neurofibromatosis 1
  • Aliases:
    • NF1
    • Peripheral Neurofibromatosis
    • Recklinghausen's neurofibromatosis
    • neurofibromatosis type I
    • von Recklinghausen Disease
Homo sapiens (human)
DOID:4992
  • optic nerve glioma
  • Aliases:
    • glioma of the optic nerve
Homo sapiens (human)
DOID:8712
  • neurofibromatosis
Homo sapiens (human)
DOID:0070483
  • Watson syndrome
Homo sapiens (human)
DOID:0111683
  • neurofibromatosis-Noonan syndrome
  • Aliases:
    • NFNS
    • Noonan neurofibromatosis syndrome
    • neurofibromatosis type 1-Noonan syndrome
    • neurofibromatosis with Noonan phenotype
Homo sapiens (human)
DOID:5151
  • plexiform neurofibroma
Homo sapiens (human)
DOID:0070482
  • spinal neurofibromatosis
  • Aliases:
    • FNSF
    • SNF
    • familial spinal neurofibromatosis
Homo sapiens (human)
DOID:0060409
  • NFIA-related disorder
  • Aliases:
    • 1p31p32 microdeletion syndrome
    • Chromosome 1, Monosomy 1p32
    • brain malformations with or without urinary tract defects
    • chromosome 1p32-p31 deletion syndrome
Homo sapiens (human)
DOID:0050858
  • Marshall-Smith syndrome
Homo sapiens (human)
DOID:0112102
  • Sotos syndrome 2
  • Aliases:
    • SOTOS2
Homo sapiens (human)
DOID:0050340
  • opportunistic bacterial infectious disease
Homo sapiens (human)
DOID:0081154
  • common variable immunodeficiency 12
Homo sapiens (human)
DOID:0081152
  • common variable immunodeficiency 10
Homo sapiens (human)
DOID:0070425
  • combined oxidative phosphorylation deficiency 52
  • Aliases:
    • COXPD52
Homo sapiens (human)
DOID:1724
  • duodenal ulcer
  • Aliases:
    • Curling Ulcer
    • Curling's ulcers
    • Stress Ulcer
Saccharomyces cerevisiae S288C
DOID:0060643
  • primary sclerosing cholangitis
Saccharomyces cerevisiae S288C
DOID:11132
  • prostatic hypertrophy
Saccharomyces cerevisiae S288C
DOID:0080526
  • bronchiectasis 1
Saccharomyces cerevisiae S288C
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

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