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 2076 - 2100 of 4621 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲
DOID:5890
  • malignant adult ependymoma
Homo sapiens (human)
DOID:5389
  • oxyphilic adenoma
  • Aliases:
    • Follicular adenoma, oxyphilic cell
    • Oncocytoma
Homo sapiens (human)
DOID:14069
  • cerebral malaria
  • Aliases:
    • Malarial encephalitis
Homo sapiens (human)
DOID:11396
  • pulmonary edema
Homo sapiens (human)
DOID:0110484
  • autosomal recessive nonsyndromic deafness 26
  • Aliases:
    • DFNB26
    • autosomal recessive deafness 26
Homo sapiens (human)
DOID:0050547
  • familial medullary thyroid carcinoma
  • Aliases:
    • THYROID CARCINOMA, FAMILIAL MEDULLARY
Homo sapiens (human)
DOID:10310
  • viral meningitis
Homo sapiens (human)
DOID:5565
  • adult teratoma
Homo sapiens (human)
DOID:3284
  • thymic carcinoma
  • Aliases:
    • Thymoma, malignant
    • malignant Thymoma
Homo sapiens (human)
DOID:1570
  • ectropion
  • Aliases:
    • Ectropion of eyelid
    • Everted margin
Homo sapiens (human)
DOID:1558
  • angioedema
  • Aliases:
    • Angioneurotic oedema
    • Quincke's edema
    • angioneurotic edema
    • giant urticaria
Homo sapiens (human)
DOID:0090087
  • hypogonadotropic hypogonadism 14 with or without anosmia
Homo sapiens (human)
DOID:12237
  • bile reflux
Homo sapiens (human)
DOID:0110268
  • cataract 22 multiple types
  • Aliases:
    • CTRCT22
Homo sapiens (human)
DOID:10548
  • cardia cancer
  • Aliases:
    • Ca cardia - stomach
    • malignant neoplasm of cardia of stomach
Homo sapiens (human)
DOID:11042
  • Felty's syndrome
  • Aliases:
    • Felty syndrome
    • Rheumatoid arthritis with splenoadenomegaly and leukopenia
Homo sapiens (human)
DOID:13375
  • temporal arteritis
  • Aliases:
    • Horton's disease
    • giant cell arteritis
Homo sapiens (human)
DOID:0110915
  • childhood hypophosphatasia
Homo sapiens (human)
DOID:229
  • female reproductive system disease
Homo sapiens (human)
DOID:0110136
  • Bardet-Biedl syndrome 14
  • Aliases:
    • BBS14
Homo sapiens (human)
DOID:6364
  • migraine
  • Aliases:
    • migraine disorder
    • migraine variant
    • migraine with or without aura
Homo sapiens (human)
DOID:0060013
  • X-linked severe combined immunodeficiency
  • Aliases:
    • SCID-X1
    • XSCID
    • gamma chain deficiency
    • thymic epithelial hypoplasia
Homo sapiens (human)
DOID:1441
  • autosomal dominant cerebellar ataxia
  • Aliases:
    • spinocerebellar ataxia
Homo sapiens (human)
DOID:0110658
  • congenital myasthenic syndrome 15
  • Aliases:
    • CMS15
    • congenital myasthenic syndrome 15 without tubular aggregates
Homo sapiens (human)
DOID:0110409
  • retinitis pigmentosa 46
  • Aliases:
    • RP46
Homo sapiens (human)

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Supported by JST NBDC Grant Number JPMJND2204

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Last updated: August 19, 2024