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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 January 28, 2025
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 2551 - 2575 of 4115 in total
Disease ID Disease Name ▲ Gene Symbol Gene ID Organism Source
DOID:0060569
  • hypertrichotic osteochondrodysplasia Cantu type
  • Aliases:
    • Cantu syndrome
Homo sapiens (human)
DOID:0110307
  • hypertrophic cardiomyopathy 1
  • Aliases:
    • CMH1
    • cardiomyopathy, familial hypertrophic 1
    • hypertrophic cardiomyopathy 19
Homo sapiens (human)
DOID:0110317
  • hypertrophic cardiomyopathy 11
  • Aliases:
    • CMH11
    • cardiomyopathy familial hypertrophic 11
Homo sapiens (human)
DOID:0110321
  • hypertrophic cardiomyopathy 15
  • Aliases:
    • CMH15
    • cardiomyopathy familial hypertrophic 15
Homo sapiens (human)
DOID:0110326
  • hypertrophic cardiomyopathy 20
  • Aliases:
    • CMH20
    • cardiomyopathy familial hypertrophic 20
Homo sapiens (human)
DOID:0110327
  • hypertrophic cardiomyopathy 26
  • Aliases:
    • CMH26
    • cardiomyopathy familial hypertrophic 26
Homo sapiens (human)
DOID:0110310
  • hypertrophic cardiomyopathy 4
  • Aliases:
    • CMH4
    • cardiomyopathy, familial hypertrophic, 4
Homo sapiens (human)
DOID:0110312
  • hypertrophic cardiomyopathy 6
  • Aliases:
    • CMH6
    • cardiomyopathy, familial hypertrophic 6
Homo sapiens (human)
DOID:0110313
  • hypertrophic cardiomyopathy 7
  • Aliases:
    • CMH7
    • cardiomyopathy, familial hypertrophic 7
Homo sapiens (human)
DOID:0110315
  • hypertrophic cardiomyopathy 9
  • Aliases:
    • CMH9
    • cardiomyopathy, familial hypertrophic, 9
Homo sapiens (human)
DOID:11984
  • hypertrophic cardiomyopathy
  • Aliases:
    • hypertrophic obstructive cardiomyopathy
Homo sapiens (human)
DOID:1920
  • hyperuricemia
  • Aliases:
    • Blood urate raized
    • uricacidemia
Homo sapiens (human)
DOID:1390
  • hypobetalipoproteinemia
  • Aliases:
    • Hypo-beta-lipoproteinemia
Homo sapiens (human)
DOID:0080041
  • hypochondroplasia
Homo sapiens (human)
DOID:11759
  • hypochromic anemia
  • Aliases:
    • ANEMIA HYPOCHROMIC
Homo sapiens (human)
DOID:0050642
  • hypochromic microcytic anemia
Homo sapiens (human)
DOID:9993
  • hypoglycemia
  • Aliases:
    • Hypoglycaemia
Homo sapiens (human)
DOID:1924
  • hypogonadism
Homo sapiens (human)
DOID:0090094
  • hypogonadotropic hypogonadism 1 with or without anosmia
  • Aliases:
    • dysplasia olfactogenitalis of de morsier
Homo sapiens (human)
DOID:0090071
  • hypogonadotropic hypogonadism 11 with or without anosmia
Homo sapiens (human)
DOID:0090075
  • hypogonadotropic hypogonadism 15 with or without anosmia
Homo sapiens (human)
DOID:0090080
  • hypogonadotropic hypogonadism 16 with or without anosmia
Homo sapiens (human)
DOID:0090076
  • hypogonadotropic hypogonadism 18 with or without anosmia
Homo sapiens (human)
DOID:0090083
  • hypogonadotropic hypogonadism 2 with or without anosmia
Homo sapiens (human)
DOID:0090082
  • hypogonadotropic hypogonadism 20 with or without anosmia
Homo sapiens (human)
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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: April 7, 2025