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 3326 - 3350 of 4621 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼
DOID:0110064
  • amelogenesis imperfecta type 1H
  • Aliases:
    • AI1H
    • amelogenesis imperfecta type IH
Homo sapiens (human)
DOID:3488
  • cellulitis
Homo sapiens (human)
DOID:1790
  • malignant mesothelioma
  • Aliases:
    • Diffuse malignant Mesothelioma
    • advanced malignant mesothelioma
    • asbestos-related malignant mesothelioma
    • malignant tumor of Mesothelium
Homo sapiens (human)
DOID:0060169
  • benign familial infantile epilepsy
  • Aliases:
    • BFIC
    • BFIE
    • benign familial infantile convulsion
    • benign familial infantile seizures
Homo sapiens (human)
DOID:263
  • kidney cancer
  • Aliases:
    • malignant neoplasm of kidney except pelvis
    • malignant tumour of kidney
    • renal cancer
Homo sapiens (human)
DOID:890
  • mitochondrial encephalomyopathy
Homo sapiens (human)
DOID:5847
  • posterior myocardial infarction
Homo sapiens (human)
DOID:5485
  • synovial sarcoma
Homo sapiens (human)
DOID:2696
  • Leydig cell tumor
  • Aliases:
    • Leydig cell neoplasm
Homo sapiens (human)
DOID:10456
  • tonsillitis
  • Aliases:
    • Throat infection - tonsillitis
    • chronic tonsillitis
Homo sapiens (human)
DOID:2001
  • neuroma
Homo sapiens (human)
DOID:0050771
  • pheochromocytoma
  • Aliases:
    • phaeochromocytoma
Homo sapiens (human)
DOID:0060285
  • parietal foramina
  • Aliases:
    • Caitlin marks
    • enlarged parietal foramina
    • hereditary cranium bifidum
Homo sapiens (human)
DOID:0060291
  • oculodentodigital dysplasia
  • Aliases:
    • ODD syndrome
Homo sapiens (human)
DOID:0060644
  • chondrodysplasia-pseudohermaphroditism syndrome
  • Aliases:
    • Nivelon-Nivelon-Mabille syndrome
    • chondrodysplasia-disorder of sex development syndrome
Homo sapiens (human)
DOID:0110797
  • hereditary spastic paraplegia 45
  • Aliases:
    • SPG45
    • SPG65
    • autosomal recessive spastic paraplegia 45
    • autosomal recessive spastic paraplegia type 45
    • autosomal recessive spastic paraplegia type 65
Homo sapiens (human)
DOID:13214
  • hole retinal cyst
  • Aliases:
    • Macular cyst or hole
    • Macular cyst, hole, or pseudohole of retina
    • Macular pseudohole retinal cyst
Homo sapiens (human)
DOID:9534
  • tuberculous pneumothorax
Homo sapiens (human)
DOID:13789
  • staphyloma posticum
Homo sapiens (human)
DOID:1485
  • cystic fibrosis
  • Aliases:
    • CF
    • mucoviscidosis
Homo sapiens (human)
DOID:0110274
  • autosomal recessive limb-girdle muscular dystrophy
Homo sapiens (human)
DOID:182
  • calcinosis
  • Aliases:
    • Pathologically calcified structure
    • pathologic calcification
Homo sapiens (human)
DOID:0070324
  • systemic Epstein-Barr virus positive T-cell lymphoma of childhood
  • Aliases:
    • EBV-positive T-cell lymphoproliferative disorder of childhood
    • systemic EBV-positive T-cell lymphoma of childhood
Homo sapiens (human)
DOID:11198
  • DiGeorge syndrome
  • Aliases:
    • 22q11.2 deletion syndrome
    • DiGeorge sequence
    • DiGeorge's syndrome
    • Pharyngeal pouch syndrome
Homo sapiens (human)
DOID:0060389
  • chromosome 10q23 deletion syndrome
Homo sapiens (human)

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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