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 3576 - 3600 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID Organism
DOID:12883
  • hypochondriasis
  • Aliases:
    • Hypochondria
    • Hypochondriacal disorder
    • hypochondriacal neurosis
Homo sapiens (human)
DOID:0060036
  • intrinsic cardiomyopathy
Drosophila melanogaster (fruit fly)
DOID:0060190
  • ileocolitis
Homo sapiens (human)
DOID:1024
  • leprosy
Rattus norvegicus (Norway rat)
DOID:0060911
  • karyomegalic interstitial nephritis
  • Aliases:
    • KIN
    • KMIN
Homo sapiens (human)
DOID:3138
  • acanthosis nigricans
  • Aliases:
    • keratosis nigricans
Homo sapiens (human)
DOID:6000
  • congestive heart failure
  • Aliases:
    • CHF
    • Cardiac Failure Congestive
    • Congestive heart disease
    • Weak heart
Rattus norvegicus (Norway rat)
DOID:2861
  • congenital nonspherocytic hemolytic anemia
  • Aliases:
    • HNSHA
    • congenital nonspherocytic hemolytic anaemia
    • hereditary nonspherocytic hemolytic anaemia
    • hereditary nonspherocytic hemolytic anemia
Homo sapiens (human)
DOID:3081
  • cystic lymphangioma
  • Aliases:
    • cystic Hygroma
Homo sapiens (human)
DOID:0050689
  • brachydactyly-syndactyly syndrome
Homo sapiens (human)
DOID:0080734
  • Ehlers-Danlos syndrome kyphoscoliotic type 1
Drosophila melanogaster (fruit fly)
DOID:12554
  • hemolytic-uremic syndrome
  • Aliases:
    • haemolytic-uraemic syndrome
    • hemolytic uremic syndrome
Homo sapiens (human)
DOID:5890
  • malignant adult ependymoma
Homo sapiens (human)
DOID:5389
  • oxyphilic adenoma
  • Aliases:
    • Follicular adenoma, oxyphilic cell
    • Oncocytoma
Homo sapiens (human)
DOID:0080557
  • congenital disorder of glycosylation Ie
  • Aliases:
    • congenital disorder of glycosylation 1e
Rattus norvegicus (Norway rat)
DOID:14069
  • cerebral malaria
  • Aliases:
    • Malarial encephalitis
Homo sapiens (human)
DOID:11396
  • pulmonary edema
Homo sapiens (human)
DOID:13317
  • hyperinsulinemic hypoglycemia
  • Aliases:
    • Islet cell hyperplasia
    • nesidioblastosis
    • persistent hyperinsulinemia hypoglycemia of infancy
Saccharomyces cerevisiae S288C
DOID:0110484
  • autosomal recessive nonsyndromic deafness 26
  • Aliases:
    • DFNB26
    • autosomal recessive deafness 26
Homo sapiens (human)
DOID:0080208
  • metabolic dysfunction-associated steatotic liver disease
  • Aliases:
    • MAFLD
    • MASLD
    • NAFLD
    • metabolic dysfunction-associated fatty liver disease
    • metabolic dysfunction-related steatotic liver disease
    • metabolic-associated fatty liver disease
    • non-alcoholic fatty liver disease
    • nonalcoholic fatty liver disease
Rattus norvegicus (Norway rat)
DOID:0111949
  • immunodeficiency 36
  • Aliases:
    • IMD36
    • activated phosphoinositide 3-kinase delta syndrome 2
Rattus norvegicus (Norway rat)
DOID:0050547
  • familial medullary thyroid carcinoma
  • Aliases:
    • THYROID CARCINOMA, FAMILIAL MEDULLARY
Homo sapiens (human)
DOID:10310
  • viral meningitis
Homo sapiens (human)
DOID:1459
  • hypothyroidism
  • Aliases:
    • Thyroid deficiency
    • Thyroid insufficiency
Drosophila melanogaster (fruit fly)
DOID:4677
  • keratitis
Mus musculus (house mouse)

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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