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 1526 - 1550 of 4621 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲
DOID:5378
  • hemoglobin D disease
  • Aliases:
    • Hb-D disease
Homo sapiens (human)
DOID:0081219
  • autosomal recessive intellectual developmental disorder 57
Homo sapiens (human)
DOID:1325
  • bronchus cancer
  • Aliases:
    • malignant neoplasm of bronchus and lung
    • malignant neoplasm of bronchus or lung
Homo sapiens (human)
DOID:12143
  • neurogenic bladder
  • Aliases:
    • Neuropathic bladder
    • neurogenic dysfunction of the urinary bladder
    • neurogenic urinary bladder disorder
Homo sapiens (human)
DOID:0110523
  • autosomal recessive nonsyndromic deafness 74
  • Aliases:
    • DFNB74
    • autosomal recessive deafness 74
Homo sapiens (human)
DOID:5854
  • silent myocardial infarction
Homo sapiens (human)
DOID:5492
  • biphasic synovial sarcoma
  • Aliases:
    • Biphasic sarcoma of Synovium
    • Synovial sarcoma, biphasic
Homo sapiens (human)
DOID:0090065
  • familial cold autoinflammatory syndrome 4
Homo sapiens (human)
DOID:4844
  • benign ependymoma
  • Aliases:
    • WHO grade II Ependymal tumor
    • epithelial ependymoma
Homo sapiens (human)
DOID:4977
  • lymphedema
  • Aliases:
    • Lymphatic edema
    • Lymphoedema
Homo sapiens (human)
DOID:1733
  • cryptosporidiosis
  • Aliases:
    • Cryptosporidial gastroenteritis
    • Infection by Cryptosporidium
    • intestinal cryptosporidiosis
Homo sapiens (human)
DOID:0070519
  • early-onset vitamin B6-dependent epilepsy 4
  • Aliases:
    • AASA dehydrogenase deficiency
    • EPEO4
    • PDE-ALDH7A1
    • antiquitin deficiency
Homo sapiens (human)
DOID:14330
  • Parkinson's disease
  • Aliases:
    • Parkinson disease
    • paralysis agitans
Homo sapiens (human)
DOID:0110110
  • atrial heart septal defect 5
  • Aliases:
    • ASD5
    • atrial septal defect 5
Homo sapiens (human)
DOID:10354
  • breast fibrocystic disease
  • Aliases:
    • Diffuse cystic mastopathy
    • Fibrocystic disease of breast
    • breast Fibrocystic Change
Homo sapiens (human)
DOID:12804
  • mucopolysaccharidosis IV
  • Aliases:
    • Mucopolysaccharidosis, MPS-IV
    • deficiency of N-acetylgalactosamine-6-sulphatase
    • deficiency of chondroitinsulphatase
    • galactosamine-6-sulfatase deficiency
Homo sapiens (human)
DOID:319
  • spinal cord disease
Homo sapiens (human)
DOID:682
  • compartment syndrome
  • Aliases:
    • Compartmental syndrome
Homo sapiens (human)
DOID:13909
  • red-green color blindness
  • Aliases:
    • Deutan defect
    • Deuteranopia
    • Reduced red-green discrimination
Homo sapiens (human)
DOID:3118
  • hepatobiliary disease
  • Aliases:
    • liver and biliary tract disease
Homo sapiens (human)
DOID:8886
  • chorioretinitis
  • Aliases:
    • retinochoroiditis
Homo sapiens (human)
DOID:4284
  • anal margin carcinoma
  • Aliases:
    • Perianal skin carcinoma
Homo sapiens (human)
DOID:727
  • premenstrual tension
Homo sapiens (human)
DOID:2842
  • Jervell-Lange Nielsen syndrome
  • Aliases:
    • Jervell and Lange-Nielson syndrome
Homo sapiens (human)
DOID:0050474
  • Netherton 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