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 3751 - 3775 of 4621 in total
Disease ID ▼ Disease Name Gene Symbol Gene ID Organism
DOID:0080221
  • obsolete major affective disorder 2
Homo sapiens (human)
DOID:0080220
  • obsolete major affective disorder 1
Homo sapiens (human)
DOID:0080218
  • primary spontaneous pneumothorax
Homo sapiens (human)
DOID:0080217
  • lysosomal acid lipase deficiency
  • Aliases:
    • LAL deficiency
    • LAL-D
Homo sapiens (human)
DOID:0080216
  • duodenal atresia
Homo sapiens (human)
DOID:0080212
  • polycystic kidney disease 4
Homo sapiens (human)
DOID:0080211
  • nodal marginal zone lymphoma
Homo sapiens (human)
DOID:0080210
  • primary mediastinal B-cell lymphoma
  • Aliases:
    • Large cell lymphoma of the mediastinum
    • Mediastinal diffuse large-cell lymphoma with sclerosis
    • Primary mediastinal clear cell lymphoma of B-cell type
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
Homo sapiens (human)
DOID:0080207
  • CAKUT2
  • Aliases:
    • Congenital anomalies of the kidney and urinary tract 2
Homo sapiens (human)
DOID:0080205
  • CAKUT
  • Aliases:
    • Congenital anomalies of the kidney and urinary tract
    • Renal or urinary tract malformation
Homo sapiens (human)
DOID:0080204
  • renal hypoplasia
Homo sapiens (human)
DOID:0080202
  • adenoid cystic carcinoma
Homo sapiens (human)
DOID:0080201
  • Peters plus syndrome
  • Aliases:
    • Krause-Kivlin syndrome
    • Peters anomaly-short limb dwarfism syndrome
    • Peters-plus syndrome
Homo sapiens (human)
DOID:0080200
  • bilateral renal aplasia
Homo sapiens (human)
DOID:0080199
  • colorectal carcinoma
Homo sapiens (human)
DOID:0080198
  • infantile histiocytoid cardiomyopathy
Homo sapiens (human)
DOID:0080197
  • congenital muscular dystrophy with cataracts and intellectual disability
Homo sapiens (human)
DOID:0080195
  • Marinesco-Sjogren syndrome
  • Aliases:
    • Garland-Moorhouse syndrome
    • Marinesco-Garland syndrome
    • Oligophrenic cerebellolenticular degeneration
    • hereditary oligophrenic cerebello-lental degeneration
Homo sapiens (human)
DOID:0080191
  • PTEN hamartoma tumor syndrome
Homo sapiens (human)
DOID:0080190
  • malignant epithelioid hemangioendothelioma
Homo sapiens (human)
DOID:0080188
  • chronic myelomonocytic leukemia
Homo sapiens (human)
DOID:0080187
  • chronic neutrophilic leukemia
Homo sapiens (human)
DOID:0080178
  • mucositis
Homo sapiens (human)
DOID:0080177
  • hepatic veno-occlusive disease
  • Aliases:
    • veno-occlusive disease
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