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 1076 - 1100 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲
DOID:682
  • compartment syndrome
  • Aliases:
    • Compartmental syndrome
Homo sapiens (human)
DOID:0070434
  • hyperphosphatasia with impaired intellectual development syndrome 2
  • Aliases:
    • GPIBD6
    • HPMRS2
    • glycosylphosphatidylinositol biosynthesis defect 6
    • hyperphosphatasia with mental retardation syndrome 2
Homo sapiens (human)
DOID:0050460
  • Wolf-Hirschhorn syndrome
  • Aliases:
    • 4p deletion syndrome
    • PITT SYNDROME
    • Pitt-Rogers-Danks Syndrome
    • chromosome 4p16.3 deletion syndrome
Homo sapiens (human)
DOID:13208
  • background diabetic retinopathy
  • Aliases:
    • Non proliferative diabetic retinopathy
    • Non-Proliferative Diabetic Retinopathy
Homo sapiens (human)
DOID:0111405
  • Fraser syndrome 1
  • Aliases:
    • FRASRS1
Homo sapiens (human)
DOID:0110178
  • Charcot-Marie-Tooth disease axonal type 2V
  • Aliases:
    • CMT2V
    • Charcot-Marie-Tooth neuropathy type 2V
    • autosomal dominant Charcot-Marie-Tooth disease type 2V
    • autosomal dominant axonal Charcot-Marie-Tooth disease type 2V
Homo sapiens (human)
DOID:0110298
  • autosomal recessive limb-girdle muscular dystrophy type 2N
  • Aliases:
    • LGMD2N
    • muscular dystrophy-dystroglycanopathy (limb-girdle) type C 2
    • muscular dystrophy-dystroglycanopathy limb-girdle POMT2-related
Homo sapiens (human)
DOID:1307
  • dementia
Homo sapiens (human)
DOID:12995
  • conduct disorder
Homo sapiens (human)
DOID:1405
  • primary angle-closure glaucoma
  • Aliases:
    • primary Angle Closure Glaucoma
Homo sapiens (human)
DOID:2986
  • IgA glomerulonephritis
  • Aliases:
    • Berger's IgA or IgG nephropathy
    • Focal Glomerulonephritis
    • IgA nephropathy
    • primary IgA nephropathy
    • segmental glomerulonephritis
Homo sapiens (human)
DOID:1495
  • cystic echinococcosis
  • Aliases:
    • Echinococcus granulosus infection
    • Echinococcus granulosus infection of lung
    • Echinococcus granulosus infection of thyroid
    • Liver echinococcus granulosus
    • Thyroid echinococcus granulosus
    • echinococcus granulosus
    • echinococcus granulosus infectious disease
    • echinococcus granulosus infectious disease of liver
    • echinococcus granulosus infectious disease of thyroid
    • lung echinococcus granulosus
    • unilocular echinococcosis
    • unilocular hydatid disease
Homo sapiens (human)
DOID:0080531
  • dedifferentiated liposarcoma
Homo sapiens (human)
DOID:1019
  • osteomyelitis
Homo sapiens (human)
DOID:1496
  • echinococcosis
  • Aliases:
    • Echinococcosis of liver
    • echinococcal disease
    • hepatic echinococcosis
    • hydatid disease
    • hydatidosis
    • liver echinococcus
    • pulmonary echinococcosis
Homo sapiens (human)
DOID:10762
  • portal hypertension
Homo sapiens (human)
DOID:6712
  • anterior spinal artery syndrome
  • Aliases:
    • Anterior spinal artery occlusion syndrome
Homo sapiens (human)
DOID:0050591
  • tooth agenesis
  • Aliases:
    • familial tooth agenesis
    • hypodontia
    • oligodontia
    • selective tooth agenesis
Homo sapiens (human)
DOID:2297
  • leptospirosis
  • Aliases:
    • Fort Bragg fever
    • Leptospirosis icterohaemorrhagica
    • Rat Catcher's Yellows
    • Weil's disease
    • nanukayami fever
    • spirochetal jaundice
Homo sapiens (human)
DOID:9834
  • hyperopia
  • Aliases:
    • Far-sightedness
    • farsightedness
    • hypermetropia
Homo sapiens (human)
DOID:9746
  • hemorrhoid
  • Aliases:
    • hemorrhoidal disease
Homo sapiens (human)
DOID:0060810
  • syndromic X-linked intellectual disability type 10
  • Aliases:
    • HSD10 deficiency, atypical type
    • HSD10 disease, atypical type
    • MRXS10
    • X-linked intellectual disability-choreoathetosis-abnormal behavior syndrome
    • mental retardation, X-linked syndromic 10
Homo sapiens (human)
DOID:4730
  • vasomotor rhinitis
Homo sapiens (human)
DOID:9042
  • polyp of corpus uteri
  • Aliases:
    • endometrial/uterine polyp
    • polyp of Endometrium
    • polyp of the Uterus
    • polyp, uterus
Homo sapiens (human)
DOID:5389
  • oxyphilic adenoma
  • Aliases:
    • Follicular adenoma, oxyphilic cell
    • Oncocytoma
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