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 15826 - 15850 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼ Source
DOID:3978
  • extrinsic cardiomyopathy
Caenorhabditis elegans
DOID:14452
  • hypokalemic periodic paralysis
  • Aliases:
    • Hypokalemic familial periodic paralysis
    • Periodic paralysis I
    • Westphal disease
    • familial hypokalemic periodic paralysis
    • periodic hypokalemic paralysis
Caenorhabditis elegans
DOID:0111458
  • galactose epimerase deficiency
  • Aliases:
    • GALE deficiency
    • GALE-D
    • UDP-galactose-4-epimerase deficiency
    • epimerase deficiency galactosemia
    • galactosemia III
    • galactosemia type 3
    • uridine diphosphate galactose-4-epimerase deficiency
Caenorhabditis elegans
DOID:0050771
  • pheochromocytoma
  • Aliases:
    • phaeochromocytoma
Caenorhabditis elegans
DOID:0070063
  • autosomal dominant intellectual developmental disorder 33
  • Aliases:
    • MRD33
    • autosomal dominant mental retardation 33
    • autosomal dominant non-syndromic intellectual disability 33
Caenorhabditis elegans
DOID:11383
  • cryptorchidism
  • Aliases:
    • Cryptorchism
    • Undescended testicle
    • Undescended testis
    • undescended testicles
Caenorhabditis elegans
DOID:0080957
  • primary hypoalphalipoproteinemia 1
  • Aliases:
    • familial HDL deficiency
    • familial hypoalphalipoproteinemia
Caenorhabditis elegans
DOID:0050697
  • chorioamnionitis
Caenorhabditis elegans
DOID:0060676
  • catecholaminergic polymorphic ventricular tachycardia 2
  • Aliases:
    • CVPT2
Caenorhabditis elegans
DOID:0070299
  • multiple epiphyseal dysplasia 5
  • Aliases:
    • BHMED
    • EDM5
    • bilateral hereditary microepiphyseal dysplasia
    • multiple epiphyseal dysplasia MATN3-related
Caenorhabditis elegans
DOID:0111153
  • congenital mirror movement disorder
  • Aliases:
    • familial congenital controlateral synkinesia
    • familial congenital mirror movements
    • hereditary congenital controlateral synkinesia
    • hereditary congenital mirror movements
    • isolated congenital controlateral synkinesia
    • isolated congenital mirror movements
Caenorhabditis elegans
DOID:9074
  • systemic lupus erythematosus
  • Aliases:
    • Lupus Erythematosus, systemic
    • SLE - Lupus Erythematosus, systemic
    • disseminated lupus erythematosus
Caenorhabditis elegans
DOID:0080557
  • congenital disorder of glycosylation Ie
  • Aliases:
    • congenital disorder of glycosylation 1e
Caenorhabditis elegans
DOID:2320
  • obstructive lung disease
  • Aliases:
    • respiratory airway obstruction
Caenorhabditis elegans
DOID:1148
  • polydactyly
  • Aliases:
    • postaxial polydactyly
Caenorhabditis elegans
DOID:3905
  • lung carcinoma
  • Aliases:
    • cancer of lung
Caenorhabditis elegans
DOID:12132
  • granulomatosis with polyangiitis
  • Aliases:
    • Necrotizing respiratory granulomatosis
    • Wegener granulomatosis, formerly
Caenorhabditis elegans
DOID:0110678
  • congenital myasthenic syndrome 4A
  • Aliases:
    • CMS Ia1
    • CMS1A1
    • CMS4A
    • congenital myasthenic syndrome 4A slow-channel
    • congenital myasthenic syndrometype Ia1
Caenorhabditis elegans
DOID:4971
  • myelofibrosis
  • Aliases:
    • Agnogenic myeloid metaplasia
    • Aleukemic myelosis
    • Megakaryocytic myelosclerosis
    • bone Marrow Fibrosis
    • myelosclerosis
    • primary myelofibrosis
Caenorhabditis elegans
DOID:2219
  • Glanzmann's thrombasthenia
  • Aliases:
    • BDPLT2
    • Glanzmann thrombasthenia
    • Glycoprotein IIb/IIIa defect
    • Thrombocytasthenia
    • deficiency of GP IIb-IIIa complex
    • deficiency of glycoprotein complex IIb-IIIa
    • deficiency of platelet fibrinogen receptor
    • platelet glycoprotein IIb-IIIa deficiency
    • platelet-type bleeding disorder 2
    • thrombasthenia of Glanzmann and Naegeli
Caenorhabditis elegans
DOID:535
  • sleep disorder
  • Aliases:
    • Non-organic sleep disorder
Caenorhabditis elegans
DOID:0110160
  • Charcot-Marie-Tooth disease axonal type 2T
  • Aliases:
    • AR-CMT2T
    • CMT2T
    • Charcot-Marie-Tooth neuropathy type 2T
    • autosomal recessive axonal Charcot-Marie-Tooth disease type 2T
Caenorhabditis elegans
DOID:0060462
  • Desbuquois dysplasia
  • Aliases:
    • Desbuquois syndrome
    • micromelic dwarfism with vertebral and metaphyseal abnormalities and advanced carpotarsal ossification
Caenorhabditis elegans
DOID:0110965
  • brachydactyly type A2
  • Aliases:
    • BDA2
    • Mohr-Wriedt type brachydactyly
    • brachymesophalangy II
Caenorhabditis elegans
DOID:12858
  • Huntington's disease
  • Aliases:
    • HD
    • Huntington disease
    • Huntington's chorea
Caenorhabditis elegans

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 v4.1.0

Last updated: December 9, 2024