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 1951 - 1975 of 4621 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼
DOID:4840
  • sebaceous carcinoma
  • Aliases:
    • Malignant Sebaceous Neoplasm
    • malignant Sebaceous tumor
    • malignant neoplasm of sebaceous gland
Homo sapiens (human)
DOID:440
  • neuromuscular disease
Homo sapiens (human)
DOID:0110293
  • autosomal recessive limb-girdle muscular dystrophy type 2P
  • Aliases:
    • LGMD2P
    • MDDGC9
    • muscular dystrophy-dystroglycanopathy (limb-girdle) type C9
    • muscular dystrophy-dystroglycanopathy limb-girdle DAG1-related
Homo sapiens (human)
DOID:1492
  • obsolete eye and adnexa disease
Homo sapiens (human)
DOID:0080762
  • autosomal recessive limb-girdle muscular dystrophy type 2Z
  • Aliases:
    • limb-girdle muscular dystrophy 21
Homo sapiens (human)
DOID:332
  • amyotrophic lateral sclerosis
  • Aliases:
    • ALS
    • Lou Gehrig's disease
    • motor neuron disease, bulbar
Homo sapiens (human)
DOID:11211
  • buphthalmos
  • Aliases:
    • primary congenital glaucoma 3A
    • simple buphthalmos
Homo sapiens (human)
DOID:1556
  • arthus reaction
  • Aliases:
    • Arthus phenomenon
    • Arthus type urticaria
Homo sapiens (human)
DOID:0050789
  • tarsal-carpal coalition syndrome
Homo sapiens (human)
DOID:0110485
  • autosomal recessive nonsyndromic deafness 27
  • Aliases:
    • DFNB27
    • autosomal recessive deafness 27
Homo sapiens (human)
DOID:0110206
  • Charcot-Marie-Tooth disease dominant intermediate F
  • Aliases:
    • CMTDIF
    • autosomal dominant intermediate Charcot-Marie-Tooth disease type F
Homo sapiens (human)
DOID:0111421
  • familial apolipoprotein A5 deficiency
  • Aliases:
    • familial APOA5 deficiency
    • familial apolipoprotein A-V deficiency
Homo sapiens (human)
DOID:0110593
  • autosomal dominant nonsyndromic deafness 9
  • Aliases:
    • DFNA9
    • autosomal dominant deafness 9
Homo sapiens (human)
DOID:0110150
  • Charcot-Marie-Tooth disease type 1D
  • Aliases:
    • CMT1D
    • Charcot-Marie-Tooth neuropathy type 1D
    • HMSN ID
    • HMSN1D
    • hereditary motor and sensory neuropathy 1D
Homo sapiens (human)
DOID:0080736
  • Ehlers-Danlos syndrome musculocontractural type 1
Homo sapiens (human)
DOID:1340
  • pure red-cell aplasia
  • Aliases:
    • Red cell hypoplasia
    • primary red cell aplasia
    • pure red cell aplasia
Homo sapiens (human)
DOID:13300
  • Scheuermann's disease
  • Aliases:
    • Juvenile osteochondritis of the spine
    • Juvenile osteochondrosis of Scheurermann
    • Juvenile osteochondrosis of spine
    • Scheuermann's kyphosis
    • Sherman's Disease
Homo sapiens (human)
DOID:13934
  • facial paralysis
  • Aliases:
    • Facial Palsy
Homo sapiens (human)
DOID:1702
  • ichthyosis vulgaris
  • Aliases:
    • Dominant congenital ichthyosiform erythroderma
Homo sapiens (human)
DOID:4247
  • coronary restenosis
Homo sapiens (human)
DOID:0060404
  • chromosome 17q12 deletion syndrome
  • Aliases:
    • 17q12 microdeletion syndrome
Homo sapiens (human)
DOID:0111531
  • bilateral optic nerve hypoplasia
  • Aliases:
    • ONH
    • familial bilateral optic nerve hypoplasia
    • isolated optic nerve hypoplasia/aplasia
Homo sapiens (human)
DOID:0110427
  • dilated cardiomyopathy 1V
  • Aliases:
    • CMD1V
Homo sapiens (human)
DOID:0050242
  • primary amebic meningoencephalitis
  • Aliases:
    • Naegleria fowleri infection
Homo sapiens (human)
DOID:11714
  • gestational diabetes
  • Aliases:
    • GDM
    • Gestational diabetes mellitus
    • Maternal gestational diabetes mellitus
Homo sapiens (human)

About Release Notes Help Feedback

Click here to visit the beta site.


International Collaboration

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


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.0.0

Last updated: August 19, 2024