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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 10651 - 10675 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲ Source
DOID:12053
  • cryptococcosis
  • Aliases:
    • Busse-Buschke's disease
    • European cryptococcosis
    • cryptococcal infection
    • torula
    • torulosis
Mus musculus (house mouse)
DOID:13689
  • prostate calculus
  • Aliases:
    • Prostatic lithiasis
    • Prostatic stone
    • Stone of prostate
    • calculus of prostate
Mus musculus (house mouse)
DOID:0060260
  • ptosis
  • Aliases:
    • blepharoptosis
    • drooping eyelid
Mus musculus (house mouse)
DOID:0050567
  • orofacial cleft
Mus musculus (house mouse)
DOID:0060652
  • familial erythrocytosis 1
  • Aliases:
    • ECYT1
    • autosomal dominant benign erythrocytosis
    • primary familial and congenital polycythemia
Mus musculus (house mouse)
DOID:0050866
  • oral squamous cell carcinoma
  • Aliases:
    • mouth squamous cell carcinoma
Mus musculus (house mouse)
DOID:0050871
  • fibroma
Mus musculus (house mouse)
DOID:0081156
  • common variable immunodeficiency 14
Mus musculus (house mouse)
DOID:0110202
  • Charcot-Marie-Tooth disease dominant intermediate A
  • Aliases:
    • CMTDIA
    • Charcot-Marie-Tooth neuropathy dominant intermediate A
    • DI-CMTA
    • autosomal dominant intermediate Charcot-Marie-Tooth disease type A
Mus musculus (house mouse)
DOID:0070219
  • familial hyperinsulinemic hypoglycemia 1
  • Aliases:
    • HHF1
Mus musculus (house mouse)
DOID:0070515
  • chromosome 16p11.2 deletion syndrome, 593-kb
  • Aliases:
    • Proximal 16p11.2 microdeletion syndrome
Mus musculus (house mouse)
DOID:5241
  • hemangioblastoma
  • Aliases:
    • Capillary Hemangioblastoma
Mus musculus (house mouse)
DOID:0112359
  • congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay
  • Aliases:
    • CAKUTHED
Mus musculus (house mouse)
DOID:0112102
  • Sotos syndrome 2
  • Aliases:
    • SOTOS2
Mus musculus (house mouse)
DOID:2537
  • inflammatory and toxic neuropathy
Mus musculus (house mouse)
DOID:12714
  • Ellis-Van Creveld syndrome
  • Aliases:
    • Chondroectodermal dysplasia
    • mesoectodermal dysplasia
Mus musculus (house mouse)
DOID:0080557
  • congenital disorder of glycosylation Ie
  • Aliases:
    • congenital disorder of glycosylation 1e
Mus musculus (house mouse)
DOID:0080055
  • achondrogenesis type IB
  • Aliases:
    • achondrogenesis Fraccaro type
Mus musculus (house mouse)
DOID:8618
  • oral cavity cancer
  • Aliases:
    • malignant neoplasm of floor of mouth
Mus musculus (house mouse)
DOID:0111402
  • mucopolysaccharidosis type IIID
  • Aliases:
    • GNS deficiency
    • MPS IIID
    • MPS3D
    • Mucopolysaccharidosis type 3D
    • N-acetylglucosamine-6-sulfatase deficiency
    • Sanfilippo syndrome D
    • Sanfilippo syndrome type D
Mus musculus (house mouse)
DOID:3326
  • purpura
  • Aliases:
    • Purpuric disorder
Mus musculus (house mouse)
DOID:0070235
  • Loeys-Dietz syndrome 1
  • Aliases:
    • AAT5
    • Furlong syndrome
    • LDS1
    • familial throacic aortic aneurysm 5
Mus musculus (house mouse)
DOID:0111343
  • lateral meningocele syndrome
  • Aliases:
    • Lehman syndrome
Mus musculus (house mouse)
DOID:11678
  • onchocerciasis
  • Aliases:
    • Infection by Onchocerca volvulus
    • Onchocerca volvulus infection
    • volvulosis
Mus musculus (house mouse)
DOID:0081399
  • autosomal dominant distal hereditary motor neuronopathy 10
Mus musculus (house mouse)
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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

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Last updated: December 9, 2024