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 5226 - 5250 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼
DOID:0110493
  • autosomal recessive nonsyndromic deafness 35
  • Aliases:
    • DFNB35
    • autosomal recessive deafness 35
Homo sapiens (human)
DOID:6676
  • Froelich syndrome
  • Aliases:
    • Babinski-Froelich syndrome
    • Froehlich syndrome
    • Froehlich's syndrome
    • Froelich's syndrome
    • adiposogenital syndrome
Homo sapiens (human)
DOID:2987
  • familial mediterranean fever
  • Aliases:
    • FMF
    • benign paroxysmal peritonitis
Homo sapiens (human)
DOID:4540
  • dysgraphia
Homo sapiens (human)
DOID:0080443
  • developmental and epileptic encephalopathy 21
  • Aliases:
    • DEE21
    • early infantile epileptic encephalopathy 21
Homo sapiens (human)
DOID:0111672
  • primary hyperoxaluria type 3
  • Aliases:
    • HP3
    • PH III
    • primary hyperoxaluria type III
Homo sapiens (human)
DOID:2562
  • suppurative periapical periodontitis
  • Aliases:
    • Apical abscess
    • Dentoalveolar abscess
    • Periapical abscess
    • Suppurative apical periodontitis
Homo sapiens (human)
DOID:0050211
  • swine influenza
Homo sapiens (human)
DOID:0080467
  • developmental and epileptic encephalopathy 2
  • Aliases:
    • DEE2
    • EIEE2
    • X-linked infantile spasm syndrome 2
    • early infantile epileptic encephalopathy 2
Homo sapiens (human)
DOID:3343
  • glycoproteinosis
  • Aliases:
    • Mucolipidosis type I
    • sialidosis
Homo sapiens (human)
DOID:8947
  • diabetic retinopathy
  • Aliases:
    • Retinal abnormality - diabetes-related
Homo sapiens (human)
DOID:0060297
  • complement component 4a deficiency
Homo sapiens (human)
DOID:11665
  • Patau syndrome
  • Aliases:
    • D1 Trisomy
    • trisomy 13
Homo sapiens (human)
DOID:0060298
  • complement component 4b deficiency
Homo sapiens (human)
DOID:0050773
  • paraganglioma
  • Aliases:
    • chemodectoma
    • glomus body tumor
Homo sapiens (human)
DOID:0050117
  • disease by infectious agent
  • Aliases:
    • infectious disease
Homo sapiens (human)
DOID:2283
  • keratopathy
Homo sapiens (human)
DOID:0110507
  • autosomal recessive nonsyndromic deafness 5
  • Aliases:
    • DFNB5
    • autosomal recessive deafness 5
Homo sapiens (human)
DOID:3193
  • peripheral nerve sheath neoplasm
  • Aliases:
    • neoplasm of the nerve Sheath
    • nerve sheath tumour
Homo sapiens (human)
DOID:4535
  • hypotrichosis
Homo sapiens (human)
DOID:5557
  • testicular germ cell cancer
  • Aliases:
    • germ cell tumor of testis
Homo sapiens (human)
DOID:13757
  • excessive tearing
  • Aliases:
    • Epiphora
    • Excessive tear production
    • Watering eye
Homo sapiens (human)
DOID:379
  • external ear disease
  • Aliases:
    • Preauricular cyst
    • Preauricular sinus and fistula
    • Preauricular sinus or fistula
Homo sapiens (human)
DOID:0090004
  • progressive pseudorheumatoid arthropathy of childhood
  • Aliases:
    • spondyloepiphyseal dysplasia tarda-progressive arthropathy syndrome
Homo sapiens (human)
DOID:0050590
  • severe congenital neutropenia
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