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 6376 - 6400 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼
DOID:3781
  • anovulation
Homo sapiens (human)
DOID:0050800
  • cerebral creatine deficiency syndrome 1
  • Aliases:
    • CEREBRAL CREATINE DEFICIENCY SYNDROME 1
    • SLC6A8 deficiency
    • creatine transporter deficiency
Homo sapiens (human)
DOID:14699
  • thrombocytopenia-absent radius syndrome
  • Aliases:
    • Radial aplasia-thrombocytopenia syndrome
    • Thrombocytopenia with absent radii (TAR) syndrome
Homo sapiens (human)
DOID:2365
  • West Nile encephalitis
  • Aliases:
    • West Nile Fever with encephalitis
    • West Nile fever encephalitis
Homo sapiens (human)
DOID:0110761
  • type 1 diabetes mellitus 24
  • Aliases:
    • IDDM24
    • Insulin-Dependent Diabetes Mellitus 24
Homo sapiens (human)
DOID:0110206
  • Charcot-Marie-Tooth disease dominant intermediate F
  • Aliases:
    • CMTDIF
    • autosomal dominant intermediate Charcot-Marie-Tooth disease type F
Homo sapiens (human)
DOID:0111420
  • familial GPIHBP1 deficiency
  • Aliases:
    • familial glycosylphosphatidylinositol-anchored high density lipoprotein-binding protein 1 deficiency
    • hyperlipoproteinemia type 1D
    • hyperlipoproteinemia type ID
Homo sapiens (human)
DOID:4176
  • blood group incompatibility
Homo sapiens (human)
DOID:10793
  • chronic sphenoidal sinusitis
  • Aliases:
    • Sphenoidal sinus-chr.
Homo sapiens (human)
DOID:0080071
  • mucolipidosis III alpha/beta
  • Aliases:
    • mucolipidosis III
    • pseudo-Hurler polydystrophy
Homo sapiens (human)
DOID:0050466
  • Loeys-Dietz syndrome
Homo sapiens (human)
DOID:14555
  • Foster-Kennedy syndrome
Homo sapiens (human)
DOID:0080693
  • Noonan syndrome-like disorder with loose anagen hair 2
Homo sapiens (human)
DOID:0111353
  • arthrogryposis, renal dysfunction, and cholestasis 1
  • Aliases:
    • ARCS1
Homo sapiens (human)
DOID:11840
  • coronary artery vasospasm
  • Aliases:
    • Coronary Vasospasm
    • Coronary artery spasm
Homo sapiens (human)
DOID:1492
  • obsolete eye and adnexa disease
Homo sapiens (human)
DOID:5505
  • papillary ependymoma
Homo sapiens (human)
DOID:9861
  • miliary tuberculosis
  • Aliases:
    • Disseminated tuberculosis
    • Tuberculosis miliaris disseminata
    • acute miliary tuberculosis
    • generalized tuberculosis
Homo sapiens (human)
DOID:0110261
  • cataract 35
  • Aliases:
    • CATCN1
    • CTRCT35
    • autosomal recessive congenital nuclear cataract 1
    • cataract 35, congenital nuclear
Homo sapiens (human)
DOID:2095
  • sweat gland cancer
  • Aliases:
    • malignant neoplasm of sweat gland
    • malignant tumor of the Sweat gland
Homo sapiens (human)
DOID:0110892
  • inflammatory bowel disease 1
  • Aliases:
    • IBD1
Homo sapiens (human)
DOID:14557
  • primary pulmonary hypertension
  • Aliases:
    • Idiopathic pulmonary arterial hypertension
Homo sapiens (human)
DOID:0112219
  • developmental and epileptic encephalopathy 84
  • Aliases:
    • DEE84
    • Jamuar syndrome
    • early infantile epileptic encephalopathy 84
Homo sapiens (human)
DOID:14686
  • Axenfeld-Rieger syndrome
  • Aliases:
    • Anomaly, Rieger's
    • Axenfeld syndrome
    • RGS - Rieger syndrome
    • Rieger's anomaly
Homo sapiens (human)
DOID:1019
  • osteomyelitis
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