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 2701 - 2725 of 4621 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Organism
DOID:12680
  • pseudobulbar palsy
  • Aliases:
    • pseudobulbar paralysis
Homo sapiens (human)
DOID:8446
  • intussusception
  • Aliases:
    • Intussusception of intestine
    • Invagination of intestine or colon
Homo sapiens (human)
DOID:0111272
  • occipital horn syndrome
  • Aliases:
    • EDS IX
    • Ehlers-Danlos syndrome type 9
    • Ehlers-Danlos syndrome type IX
    • X-linked cutis laxa
Homo sapiens (human)
DOID:9775
  • diastolic heart failure
Homo sapiens (human)
DOID:7608
  • parathyroid adenoma
  • Aliases:
    • adenoma of the Parathyroid gland
Homo sapiens (human)
DOID:1540
  • parathyroid carcinoma
  • Aliases:
    • Parathyroid gland neoplasm
    • carcinoma of Parathyroid gland
    • malignant neoplasm of parathyroid gland
    • malignant neoplasm of the Parathyroid
    • malignant tumor of parathyroid gland
    • neoplasm of parathyroid gland
    • parathyroid gland cancer
    • parathyroid neoplasm
Homo sapiens (human)
DOID:0080886
  • vitamin D-dependent rickets type 1A
Homo sapiens (human)
DOID:1564
  • fungal infectious disease
  • Aliases:
    • mycosis
Homo sapiens (human)
DOID:8913
  • dermatophytosis
Homo sapiens (human)
DOID:9146
  • visceral leishmaniasis
  • Aliases:
    • Infection by visceral leishmaniasis
    • Kala-Azar
Homo sapiens (human)
DOID:9065
  • leishmaniasis
Homo sapiens (human)
DOID:2789
  • parasitic protozoa infectious disease
  • Aliases:
    • mastigophora infectious disease
    • sarcomastigophora infectious disease
Homo sapiens (human)
DOID:0080159
  • Cryptococcal meningitis
Homo sapiens (human)
DOID:0050242
  • primary amebic meningoencephalitis
  • Aliases:
    • Naegleria fowleri infection
Homo sapiens (human)
DOID:4189
  • mutism
Homo sapiens (human)
DOID:12971
  • hereditary spherocytosis
  • Aliases:
    • Congenital spherocytic hemolytic anemia
    • Minkowski Chauffard syndrome
    • spherocytic anemia
Homo sapiens (human)
DOID:10393
  • secondary hypertrophic osteoarthropathy
  • Aliases:
    • Bamberger-Marie disease
    • HPOA - hypertrophic pulmonary osteoarthropathy
    • Marie Bamberger disease
    • hypertrophic pulmonary osteoarthropathy
Homo sapiens (human)
DOID:2373
  • hereditary elliptocytosis
  • Aliases:
    • Congenital elliptocytosis
    • ovalocytosis
Homo sapiens (human)
DOID:589
  • congenital hemolytic anemia
  • Aliases:
    • congenital hemolytic anaemia
    • hereditary hemolytic anaemia
    • hereditary hemolytic anemia
Homo sapiens (human)
DOID:13628
  • favism
Homo sapiens (human)
DOID:583
  • hemolytic anemia
  • Aliases:
    • ANEMIA HEMOLYTIC
Homo sapiens (human)
DOID:2583
  • agammaglobulinemia
  • Aliases:
    • IGHM
    • hypogammaglobulinemia
    • mu heavy chain deficiency
Homo sapiens (human)
DOID:1098
  • fetal erythroblastosis
  • Aliases:
    • EF - Erythroblastosis foetalis
    • Haemolytic disease due to rhesus isoimmunisation
    • erythroblastosis fetalis
    • rhesus isoimmunisation of the newborn
Homo sapiens (human)
DOID:2860
  • hemoglobinopathy
  • Aliases:
    • hemoglobinopathies
Homo sapiens (human)
DOID:8437
  • intestinal obstruction
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