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 4826 - 4850 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Organism
DOID:4404
  • occupational dermatitis
  • Aliases:
    • Occupational allergic contact dermatitis
    • Occupational eczema
Homo sapiens (human)
DOID:2773
  • contact dermatitis
  • Aliases:
    • Contact dermatitis/eczema
    • Contact eczema
    • Dermatitis, venenata
    • dermatitis venenata
Homo sapiens (human)
DOID:2712
  • phimosis
  • Aliases:
    • Tight foreskin
    • Tight frenulum
Homo sapiens (human)
DOID:0050448
  • white sponge nevus
  • Aliases:
    • hereditary mucosal leukokeratosis
    • white sponge nevus of Cannon
Homo sapiens (human)
DOID:9655
  • oral mucosa leukoplakia
Homo sapiens (human)
DOID:750
  • peptic ulcer disease
  • Aliases:
    • acute peptic ulcer with hemorrhage
    • acute peptic ulcer with hemorrhage and perforation
    • acute peptic ulcer without hemorrhage and without perforation
Homo sapiens (human)
DOID:229
  • female reproductive system disease
Homo sapiens (human)
DOID:0050689
  • brachydactyly-syndactyly syndrome
Homo sapiens (human)
DOID:10908
  • hydrocephalus
  • Aliases:
    • hydrocephalus, X-linked
    • hydrocephalus, nonsyndromic, autosomal recessive
Mus musculus (house mouse)
DOID:234
  • colon adenocarcinoma
  • Aliases:
    • Colonic adenocarcinoma
    • adenocarcinoma of colon
Mus musculus (house mouse)
DOID:3526
  • cerebral infarction
  • Aliases:
    • CVA - Cerebral infarction
    • Cerebral infarct
Mus musculus (house mouse)
DOID:13603
  • obstructive jaundice
  • Aliases:
    • Cholestatic Jaundice
    • Cholestatic jaundice syndrome
    • Obstructive hyperbilirubinemia
Mus musculus (house mouse)
DOID:11446
  • sciatic neuropathy
Mus musculus (house mouse)
DOID:0050948
  • autosomal dominant hypophosphatemic rickets
Homo sapiens (human)
DOID:1100
  • ovarian disease
Homo sapiens (human)
DOID:0110741
  • type 1 diabetes mellitus 2
  • Aliases:
    • IDDM2
    • Insulin-Dependent Diabetes Mellitus 2
Mus musculus (house mouse)
DOID:0110196
  • Charcot-Marie-Tooth disease type 4G
  • Aliases:
    • CMT4G
    • Charcot-Marie-Tooth neuropathy type 4G
    • HMSNR
    • autosomal recessive Charcot-Marie-Tooth disease type 4G
    • hereditary motor and sensory neuropathy Russe type
Mus musculus (house mouse)
DOID:10923
  • sickle cell anemia
  • Aliases:
    • Hb SC disease
    • Hb-S/Hb-C disease
    • Hb-SS disease without crisis
    • Hemoglobin S disease without crisis
    • Sickle-cell/Hb-C disease without crisis
    • drepanocytosis
    • haemoglobin SC disease
    • hemoglobin SC disease
    • sickle cell anaemia
Mus musculus (house mouse)
DOID:10584
  • retinitis pigmentosa
  • Aliases:
    • pericentral pigmentary retinopathy
Mus musculus (house mouse)
DOID:0080029
  • autosomal recessive spinocerebellar ataxia 16
  • Aliases:
    • SCAR16
Homo sapiens (human)
DOID:3211
  • lysosomal storage disease
  • Aliases:
    • disorder of lysosomal enzyme
    • inborn lysosomal enzyme disorder
    • lysosomal storage metabolism disorder
Mus musculus (house mouse)
DOID:3323
  • Sandhoff disease
  • Aliases:
    • Sandhoff Jatzkewitz disease
Mus musculus (house mouse)
DOID:12377
  • spinal muscular atrophy
Mus musculus (house mouse)
DOID:3320
  • Tay-Sachs disease
  • Aliases:
    • GM2 gangliosidosis, type 1
    • hexosaminidase A deficiency
Mus musculus (house mouse)
DOID:9409
  • diabetes insipidus
Mus musculus (house mouse)

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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