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 3126 - 3150 of 4621 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Organism
DOID:3753
  • Hermansky-Pudlak syndrome
Homo sapiens (human)
DOID:0111168
  • sepiapterin reductase deficiency
  • Aliases:
    • DRD due to SRD
    • SPR deficiency
    • SRD
    • dopa-responsive dystonia due to sepiapterin reductase deficiency
Homo sapiens (human)
DOID:0050433
  • fatal familial insomnia
Homo sapiens (human)
DOID:11695
  • portal vein thrombosis
Homo sapiens (human)
DOID:0050685
  • small cell carcinoma
  • Aliases:
    • Small cell carcinoma - intermediate cell
    • Small cell carcinoma, intermediate cell
    • intermediate cell small cell carcinoma
Homo sapiens (human)
DOID:639
  • acute disseminated encephalomyelitis
  • Aliases:
    • ADEM
    • acute disseminated encephalitis
Homo sapiens (human)
DOID:13664
  • post-vaccinal encephalitis
  • Aliases:
    • Encephalitis following immunization procedures
    • Postvaccinal encephalomyelitis
Homo sapiens (human)
DOID:11204
  • allergic conjunctivitis
Homo sapiens (human)
DOID:2474
  • vernal conjunctivitis
Homo sapiens (human)
DOID:2457
  • giant papillary conjunctivitis
Homo sapiens (human)
DOID:0050127
  • sinusitis
Homo sapiens (human)
DOID:13078
  • eumycotic mycetoma
  • Aliases:
    • Madura foot
    • Maduromycosis, mycotic
    • Mycotic mycetoma
    • eumycetoma
    • maduromycosis
Homo sapiens (human)
DOID:0070112
  • Niemann-Pick disease type B
Homo sapiens (human)
DOID:0070111
  • Niemann-Pick disease type A
Homo sapiens (human)
DOID:14223
  • ochronosis
Homo sapiens (human)
DOID:9270
  • alkaptonuria
  • Aliases:
    • Homogentisate 1,2-dioxygenase deficiency
    • alcaptonuria
Homo sapiens (human)
DOID:0080211
  • nodal marginal zone lymphoma
Homo sapiens (human)
DOID:12841
  • ancylostomiasis
Homo sapiens (human)
DOID:0050912
  • colon adenoma
Homo sapiens (human)
DOID:3762
  • cytochrome-c oxidase deficiency disease
  • Aliases:
    • MITOCHONDRIAL COMPLEX IV DEFICIENCY
Homo sapiens (human)
DOID:12399
  • pathological gambling
  • Aliases:
    • Compulsive gambling
Homo sapiens (human)
DOID:0060235
  • carnitine palmitoyltransferase II deficiency
  • Aliases:
    • CPT-II
    • infantile carnitine palmitoyltransferase II deficiency
    • late-onset carnitine palmitoyltransferase II deficiency
    • lethal neonatal carnitine palmitoyltransferase II deficiency
Homo sapiens (human)
DOID:0050469
  • Costello syndrome
  • Aliases:
    • FCS SYNDROME
    • Faciocutaneoskeletal Syndrome
Homo sapiens (human)
DOID:1673
  • pneumothorax
Homo sapiens (human)
DOID:14775
  • brittle cornea syndrome 1
  • Aliases:
    • type VIB Ehlers-Danlos 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