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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 10751 - 10775 of 15957 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism Source
DOID:0111167
  • Dyggve-Melchior-Clausen disease
  • Aliases:
    • DMC disease
    • pseudo-Morquio disease type I
Homo sapiens (human)
DOID:0060247
  • Smith-McCort dysplasia
Homo sapiens (human)
DOID:0060767
  • autosomal dominant Robinow syndrome 3
  • Aliases:
    • DRS3
Homo sapiens (human)
DOID:0060765
  • autosomal dominant Robinow syndrome 2
  • Aliases:
    • DRS2
Homo sapiens (human)
DOID:0112184
  • thyroid dyshormonogenesis 5
  • Aliases:
    • TDH5
    • genetic defect in thyroid hormonogenesis 5
Homo sapiens (human)
DOID:0112189
  • thyroid dyshormonogenesis 6
  • Aliases:
    • TDH6
    • genetic defect in thyroid hormonogenesis 6
Homo sapiens (human)
DOID:1498
  • cholera
  • Aliases:
    • Cholera - Vibrio cholerae
    • Cholera due to Vibrio cholerae
    • Vibrio cholerae
Homo sapiens (human)
DOID:0050338
  • primary bacterial infectious disease
Homo sapiens (human)
DOID:0060545
  • Hermansky-Pudlak syndrome 7
Homo sapiens (human)
DOID:0110774
  • hereditary spastic paraplegia 23
  • Aliases:
    • Lison syndrome
    • SPG23
    • Spastic paraparesis-vitiligo-premature graying-characteristic facies syndrome
    • spastic paraplegia 23
    • spastic paraplegia with pigmentary abnormalities
Homo sapiens (human)
DOID:0080206
  • CAKUT1
  • Aliases:
    • Congenital anomalies of the kidney and urinary tract 1
Homo sapiens (human)
DOID:0070151
  • hereditary sensory and autonomic neuropathy type 6
  • Aliases:
    • HSAN6
    • hereditary sensory and autonomic neuropathy type VI
Homo sapiens (human)
DOID:0110076
  • arrhythmogenic right ventricular dysplasia 8
  • Aliases:
    • ARVC8
    • ARVD8
    • arrhythmogenic right ventricular cardiomyopathy 8
    • familial arrhythmogenic right ventricular dysplasia 8
Homo sapiens (human)
DOID:0090128
  • Carvajal syndrome
  • Aliases:
    • DCWHK
    • dilated cardiomyopathy with woolly hair and keratoderma
    • palmoplantar keratoderma with left ventricular cardiomyopathy and woolly hair
Homo sapiens (human)
DOID:0081109
  • keratosis palmoplantaris striata 2
Homo sapiens (human)
DOID:0110703
  • hypotrichosis 6
  • Aliases:
    • Hypotrichosis, Localized, Autosomal Recessive 1
    • Hypt6
    • Lah1
    • Monilethrix-like hypotrichosis
    • autosomal recessive localized hypotrichosis
Homo sapiens (human)
DOID:4535
  • hypotrichosis
Homo sapiens (human)
DOID:0060851
  • pemphigus vulgaris
  • Aliases:
    • familial pemphigus vulgaris
Homo sapiens (human)
DOID:0110458
  • dilated cardiomyopathy 1BB
  • Aliases:
    • CMD1BB
Homo sapiens (human)
DOID:0110081
  • arrhythmogenic right ventricular dysplasia 10
  • Aliases:
    • ARVC10
    • ARVD10
    • arrhythmogenic right ventricular cardiomyopathy 10
    • familial arrhythmogenic right ventricular dysplasia 10
Homo sapiens (human)
DOID:0081108
  • keratosis palmoplantaris striata 1
Homo sapiens (human)
DOID:0080737
  • Ehlers-Danlos syndrome musculocontractural type 2
Homo sapiens (human)
DOID:0110082
  • arrhythmogenic right ventricular dysplasia 11
  • Aliases:
    • ARVC11
    • ARVD11
    • arrhythmogenic right ventricular cardiomyopathy 11
    • familial arrhythmogenic right ventricular dysplasia 11
Homo sapiens (human)
DOID:529
  • blepharospasm
Homo sapiens (human)
DOID:0060040
  • pervasive developmental disorder
  • Aliases:
    • Pervasive Child Development Disorders
    • pervasive development disorder
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: December 9, 2024