GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB), DisGeNET, and Alliance of Genome Resources is integrated into one list.

Source Last Updated
Alliance of Genome Resources July 29, 2024
DisGeNET July 29, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 1551 - 1575 of 4621 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲
DOID:3042
  • allergic contact dermatitis
Homo sapiens (human)
DOID:0090058
  • torsion dystonia with onset in infancy
Homo sapiens (human)
DOID:9563
  • bronchiectasis
  • Aliases:
    • Polynesian bronchiectasis
Homo sapiens (human)
DOID:7848
  • interdigitating dendritic cell sarcoma
  • Aliases:
    • Interdigitating cell sarcoma
Homo sapiens (human)
DOID:0110487
  • autosomal recessive nonsyndromic deafness 29
  • Aliases:
    • DFNB29
    • autosomal recessive deafness 29
Homo sapiens (human)
DOID:10095
  • intracranial abscess
Homo sapiens (human)
DOID:3443
  • mammary Paget's disease
  • Aliases:
    • Paget cell neoplasm
    • Paget's disease
    • Paget's disease of the breast
    • mammary Paget disease
Homo sapiens (human)
DOID:0111136
  • congenital generalized lipodystrophy type 2
  • Aliases:
    • Berardinelli-Seip congenital lipodystrophy type 2
    • Berardinelli-Seip syndrome
    • Brunzell syndrome BSCL2-related
    • CGL2
    • congenital lipoatrophic diabetes
    • total lipodystrophy and acromegaloid gigantism
Homo sapiens (human)
DOID:0080021
  • Schmid metaphyseal chondrodysplasia
  • Aliases:
    • Japanese type spondylometaphyseal dysplasia
    • Schmid type metaphyseal dysplasia
Homo sapiens (human)
DOID:0112105
  • X-linked parkinsonism-spasticity syndrome
  • Aliases:
    • X-linked Parkinsonism with spasticity
    • XPDS
Homo sapiens (human)
DOID:2602
  • chondroma
  • Aliases:
    • central Chondroma
Homo sapiens (human)
DOID:8504
  • impetigo
Homo sapiens (human)
DOID:2065
  • syringoma
Homo sapiens (human)
DOID:0110813
  • hereditary spastic paraplegia 62
  • Aliases:
    • SPG62
    • autosomal recessive spastic paraplegia 62
    • autosomal recessive spastic paraplegia type 62
Homo sapiens (human)
DOID:678
  • progressive supranuclear palsy
  • Aliases:
    • Steele-Richardson-Olszewski syndrome
    • progressive supranuclear ophthalmoplegia
Homo sapiens (human)
DOID:6869
  • parasagittal meningioma
Homo sapiens (human)
DOID:11100
  • Q fever
  • Aliases:
    • Infection due to Coxiella burnetii
Homo sapiens (human)
DOID:13501
  • Moebius syndrome
  • Aliases:
    • Mobius syndrome
    • Moebius congenital oculofacial paralysis
    • Oromandibular-limb hypogenesis spectrum
Homo sapiens (human)
DOID:0060422
  • chromosome 6pter-p24 deletion syndrome
  • Aliases:
    • 6p subtelomeric deletion syndrome
    • 6p25 microdeletion syndrome
    • distal monosomy 6p
Homo sapiens (human)
DOID:9341
  • urethral diverticulum
Homo sapiens (human)
DOID:631
  • fibromyalgia
Homo sapiens (human)
DOID:0090089
  • hypogonadotropic hypogonadism 10 with or without anosmia
Homo sapiens (human)
DOID:0110301
  • obsolete autosomal dominant limb-girdle muscular dystrophy type 1B
Homo sapiens (human)
DOID:0070216
  • familial hyperinsulinemic hypoglycemia 3
  • Aliases:
    • HHF3
    • hyperinsulinemic hypoglycemia due to glucokinase deficiency
    • hyperinsulinism due to glucokinase deficiency
Homo sapiens (human)
DOID:1754
  • mitral valve stenosis
  • Aliases:
    • Mitral stenosis
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: August 19, 2024