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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 4426 - 4450 of 4649 in total
Disease ID Disease Name ▼ Gene Symbol Gene ID Organism Source
DOID:6457
  • Cowden syndrome
  • Aliases:
    • Cowden disease
    • Lhermitte-Duclos disease
    • dysplastic Gangliocytoma of Cerebellum
Homo sapiens (human)
DOID:0081003
  • Cowden syndrome 7
Homo sapiens (human)
DOID:0081002
  • Cowden syndrome 6
Homo sapiens (human)
DOID:0081001
  • Cowden syndrome 5
Homo sapiens (human)
DOID:0050469
  • Costello syndrome
  • Aliases:
    • FCS SYNDROME
    • Faciocutaneoskeletal Syndrome
Homo sapiens (human)
DOID:0080599
  • Coronavirus infectious disease
Homo sapiens (human)
DOID:11725
  • Cornelia de Lange syndrome
  • Aliases:
    • Brachmann de Lange syndrome
    • De Lange syndrome
Homo sapiens (human)
DOID:0080507
  • Cornelia de Lange syndrome 3
  • Aliases:
    • CDLS3
    • Cornelia De Lange syndrome 3 with or without midline brain defects
Homo sapiens (human)
DOID:0080506
  • Cornelia de Lange syndrome 2
Homo sapiens (human)
DOID:0080505
  • Cornelia de Lange syndrome 1
Homo sapiens (human)
DOID:8515
  • Cor pulmonale
  • Aliases:
    • cardiopulmonary disease
    • pulmonary heart disease
Homo sapiens (human)
DOID:0080101
  • Compton-North congenital myopathy
  • Aliases:
    • congenital myopathy 12
Homo sapiens (human)
DOID:0060438
  • Cole-Carpenter syndrome
Homo sapiens (human)
DOID:0111590
  • Cohen syndrome
  • Aliases:
    • COH1
    • Hypotonia, obesity, and prominent incisors
    • Pepper syndrome
Homo sapiens (human)
DOID:1925
  • Coffin-Siris syndrome
  • Aliases:
    • Dwarfism-Onychodysplasia
    • Fifth Digit Syndrome
    • Short Stature-Onychodysplasia.
Homo sapiens (human)
DOID:0112367
  • Coffin-Siris syndrome 8
  • Aliases:
    • CSS8
Homo sapiens (human)
DOID:0080297
  • Coffin-Siris syndrome 6
Homo sapiens (human)
DOID:0112368
  • Coffin-Siris syndrome 5
  • Aliases:
    • CSS5
Homo sapiens (human)
DOID:0070046
  • Coffin-Siris syndrome 4
  • Aliases:
    • CSS4
    • MRD16
    • autosomal dominant mental retardation 16
Homo sapiens (human)
DOID:0070045
  • Coffin-Siris syndrome 3
  • Aliases:
    • CSS3
    • MRD15
    • autosomal dominant mental retardation 15
Homo sapiens (human)
DOID:0070044
  • Coffin-Siris syndrome 2
  • Aliases:
    • CSS2
    • MRD14
    • autosomal dominant mental retardation 14
Homo sapiens (human)
DOID:0112370
  • Coffin-Siris syndrome 12
  • Aliases:
    • CSS12
Homo sapiens (human)
DOID:0112372
  • Coffin-Siris syndrome 11
  • Aliases:
    • CSS11
Homo sapiens (human)
DOID:0070042
  • Coffin-Siris syndrome 1
  • Aliases:
    • CSS1
    • MRD12
    • autosomal dominant mental retardation 12
    • fifth digit syndrome
Homo sapiens (human)
DOID:3783
  • Coffin-Lowry syndrome
Homo sapiens (human)
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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: February 17, 2025