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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 8451 - 8475 of 15957 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism Source
DOID:2797
  • idiopathic interstitial pneumonia
  • Aliases:
    • Diffuse idiopathic pulmonary fibrosis
    • Idiopathic fibrosing alveolitis
Homo sapiens (human)
DOID:3904
  • bronchus carcinoma
  • Aliases:
    • BC - Bronchogenic carcinoma
Homo sapiens (human)
DOID:0080135
  • multiple mitochondrial dysfunctions syndrome 3
  • Aliases:
    • IBA57 deficiency
Homo sapiens (human)
DOID:0110819
  • hereditary spastic paraplegia 74
  • Aliases:
    • SPG74
    • autosomal recessive spastic paraplegia 74
Homo sapiens (human)
DOID:0111974
  • immunodeficiency 59
  • Aliases:
    • IMD59
    • granulocytopenia with immunoglobin abnormality
    • immunodeficiency 59 and hypoglycemia
Rattus norvegicus (Norway rat)
DOID:0111974
  • immunodeficiency 59
  • Aliases:
    • IMD59
    • granulocytopenia with immunoglobin abnormality
    • immunodeficiency 59 and hypoglycemia
Mus musculus (house mouse)
DOID:0060793
  • hypomyelinating leukodystrophy 5
  • Aliases:
    • HLD5
    • hypomyelination-congenital cataract syndrome
Mus musculus (house mouse)
DOID:0050809
  • mucopolysaccharidosis IX
Rattus norvegicus (Norway rat)
DOID:0050809
  • mucopolysaccharidosis IX
Mus musculus (house mouse)
DOID:0060811
  • syndromic X-linked intellectual disability Turner type
  • Aliases:
    • Brooks-Wisniewski-Brown syndrome
    • MRXST
    • X-linked intellectual disability, Brooks type
    • mental retardation and macrocephaly syndrome
    • mental retardation, X-linked syndromic, Turner type
Mus musculus (house mouse)
DOID:0060309
  • syndromic X-linked intellectual disability
  • Aliases:
    • syndromic X-linked mental retardation
Mus musculus (house mouse)
DOID:8689
  • anorexia nervosa
Rattus norvegicus (Norway rat)
DOID:8689
  • anorexia nervosa
Mus musculus (house mouse)
DOID:11983
  • Prader-Willi syndrome
  • Aliases:
    • Prader Willi syndrome
Rattus norvegicus (Norway rat)
DOID:11983
  • Prader-Willi syndrome
  • Aliases:
    • Prader Willi syndrome
Mus musculus (house mouse)
DOID:252
  • alcoholic psychosis
  • Aliases:
    • Alcoholic psychoses
Rattus norvegicus (Norway rat)
DOID:2537
  • inflammatory and toxic neuropathy
Rattus norvegicus (Norway rat)
DOID:252
  • alcoholic psychosis
  • Aliases:
    • Alcoholic psychoses
Mus musculus (house mouse)
DOID:2537
  • inflammatory and toxic neuropathy
Mus musculus (house mouse)
DOID:12995
  • conduct disorder
Rattus norvegicus (Norway rat)
DOID:10939
  • antisocial personality disorder
  • Aliases:
    • Asocial personality
    • Dissocial personality disorder
    • Psychopath.personality
    • Psychopathic personality
    • Psychopathic personality disorder
    • sociopathic personality
Rattus norvegicus (Norway rat)
DOID:13481
  • thanatophoric dysplasia
Mus musculus (house mouse)
DOID:0090032
  • Silverman-Handmaker type dyssegmental dysplasia
Mus musculus (house mouse)
DOID:0090005
  • Schwartz-Jampel syndrome 1
  • Aliases:
    • Aberfeld syndrome
    • Burton skeletal dysplasia
    • Burton syndrome
    • Catel-Hempel syndrome
    • Catel-Hempel type dysostosis enchondralis metaepiphysaria
    • Schwartz-Jampel syndrome type 1
    • Schwartz-Jampel-Aberfeld syndrome
    • myotonic chondrodystrophy
    • myotonic myopathy, dwarfism, chondrodystrophy, ocular and facial anomalies
    • osteochondromuscular dystrophy
Mus musculus (house mouse)
DOID:0060789
  • hypomyelinating leukodystrophy 4
  • Aliases:
    • HLD4
    • MitCHAP60 disease
    • Pelizaeus-Merzbacher-like disease due to HSPD1 mutation
    • mitochondrial HSP60 chaperonopathy
Rattus norvegicus (Norway rat)
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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