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 1026 - 1050 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:4914
  • esophagus adenocarcinoma
  • Aliases:
    • Oesophageal adenocarcinoma
Mus musculus (house mouse)
DOID:0080887
  • vitamin D-dependent rickets type 1B
Homo sapiens (human)
DOID:0112045
  • non-syndromic X-linked intellectual disability 93
  • Aliases:
    • MRX93
    • X-linked mental retardation 93
    • X-linked mental retardation with macrocephaly
Homo sapiens (human)
DOID:0111481
  • combined oxidative phosphorylation deficiency 11
  • Aliases:
    • COXPD11
    • infantile encephaloneuromyopathy due to mitochondrial translation defect
Homo sapiens (human)
DOID:0090078
  • hypogonadotropic hypogonadism 7 with or without anosmia
Rattus norvegicus (Norway rat)
DOID:12176
  • goiter
  • Aliases:
    • goitre
Drosophila melanogaster (fruit fly)
DOID:0080504
  • Parkinson's disease 22
  • Aliases:
    • autosomal dominant Parkinson's disease 22
Mus musculus (house mouse)
DOID:0111936
  • immunodeficiency 14
  • Aliases:
    • APDS
    • IMD14
    • PASLI disease
    • activated PI3K-delta syndrome
    • senescent T-cells-lymphadenopathy-immunodeficiency syndrome due to p110delta-activating mutation
Homo sapiens (human)
DOID:4483
  • rhinitis
Danio rerio (zebrafish)
DOID:784
  • chronic kidney disease
  • Aliases:
    • CKD
    • CRF
    • chronic kidney failure
    • chronic renal disease
    • chronic renal failure syndrome
    • renal failure - chronic
Mus musculus (house mouse)
DOID:0110629
  • Wolfram syndrome 1
  • Aliases:
    • DIDMOAD
    • WFS1
    • diabetes mellitus AND insipidus with optic atrophy AND deafness
Homo sapiens (human)
DOID:2300
  • spondylolysis
Rattus norvegicus (Norway rat)
DOID:399
  • tuberculosis
Rattus norvegicus (Norway rat)
DOID:0080163
  • otulipenia
  • Aliases:
    • autoinflammation, panniculitis and dermatosis syndrome
    • otulin-related autoinflammatory syndrome
Homo sapiens (human)
DOID:0080096
  • myofibrillar myopathy 5
  • Aliases:
    • filaminopathy
Mus musculus (house mouse)
DOID:0090045
  • childhood onset GLUT1 deficiency syndrome 2
Homo sapiens (human)
DOID:0110539
  • autosomal recessive nonsyndromic deafness 97
  • Aliases:
    • DFNB97
    • autosomal recessive deafness 97
Mus musculus (house mouse)
DOID:0111861
  • Meester-Loeys syndrome
  • Aliases:
    • MRLS
Rattus norvegicus (Norway rat)
DOID:0112374
  • muscular dystrophy-dystroglycanopathy
  • Aliases:
    • MDDG
Saccharomyces cerevisiae S288C
DOID:0081183
  • autosomal recessive intellectual developmental disorder 7
Drosophila melanogaster (fruit fly)
DOID:7475
  • diverticulitis
Mus musculus (house mouse)
DOID:0110042
  • Alzheimer's disease 3
  • Aliases:
    • AD3
    • Alzheimer disease 3
    • Alzheimer disease 3, early onset
    • Alzheimer disease familial 3
Homo sapiens (human)
DOID:0111258
  • pentosuria
  • Aliases:
    • L-xylulose reductase deficiency
    • L-xylulosuria
    • PNTSU
    • essential pentosuria
    • xylitol dehydrogenase deficiency
Homo sapiens (human)
DOID:0111526
  • Mullerian aplasia and hyperandrogenism
  • Aliases:
    • Mullerian duct failure and hyperandrogenism
    • WNT4 deficiency
Homo sapiens (human)
DOID:0111504
  • Li-Fraumeni syndrome 2
  • Aliases:
    • LFS2
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