GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB) and Alliance of Genome Resources is integrated into one list.

Source Last Updated
Alliance of Genome Resources October 9, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 6251 - 6275 of 15957 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism Source
DOID:1596
  • depressive disorder
  • Aliases:
    • mental depression
Saccharomyces cerevisiae S288C
DOID:446
  • primary hyperaldosteronism
  • Aliases:
    • Cushing syndrome
    • Cushing's syndrome
    • hyperaldosteronism
Saccharomyces cerevisiae S288C
DOID:10825
  • essential hypertension
  • Aliases:
    • idiopathic hypertension
    • primary hypertension
Saccharomyces cerevisiae S288C
DOID:0060224
  • atrial fibrillation
  • Aliases:
    • A-fib
    • AFib
Saccharomyces cerevisiae S288C
DOID:0080827
  • human cytomegalovirus infection
Saccharomyces cerevisiae S288C
DOID:14503
  • neuronal ceroid lipofuscinosis
  • Aliases:
    • hereditary ceroid lipofuscinosis
Saccharomyces cerevisiae S288C
DOID:0110725
  • neuronal ceroid lipofuscinosis 10
  • Aliases:
    • CLN10
    • Cathepsin D deficiency
    • neuronal ceroid lipofuscinosis cathepsin D-deficient
    • neuronal ceroid lipofuscinosis due to cathepsin D deficiency
Saccharomyces cerevisiae S288C
DOID:10762
  • portal hypertension
Saccharomyces cerevisiae S288C
DOID:1591
  • renovascular hypertension
Saccharomyces cerevisiae S288C
DOID:0090060
  • Wolcott-Rallison syndrome
Drosophila melanogaster (fruit fly)
DOID:5453
  • pulmonary venoocclusive disease
  • Aliases:
    • pulmonary veno-occlusive disease
Drosophila melanogaster (fruit fly)
DOID:9643
  • babesiosis
  • Aliases:
    • Babesiasis
    • Infection by babesia
    • piroplasmosis
Homo sapiens (human)
DOID:0111635
  • autosomal recessive nonsyndromic deafness 57
  • Aliases:
    • DFNB57
    • autosomal recessive deafness 57
Homo sapiens (human)
DOID:0110838
  • Usher syndrome type 2A
  • Aliases:
    • USH2A
    • Usher syndrome type IIA
Homo sapiens (human)
DOID:0111103
  • maturity-onset diabetes of the young type 4
  • Aliases:
    • MODY type 4
    • MODY4
Homo sapiens (human)
DOID:0050877
  • pancreatic agenesis
  • Aliases:
    • Agenesis of the dorsal pancreas
    • partial pancreatic agenesis
Homo sapiens (human)
DOID:3304
  • germinoma
Homo sapiens (human)
DOID:0111344
  • myeloproliferative disorder with eosinophilia
  • Aliases:
    • chronic myeloproliferative disorder with eosinophilia
Homo sapiens (human)
DOID:8946
  • severe nonproliferative diabetic retinopathy
  • Aliases:
    • High risk non proliferative diabetic retinopathy
    • Severe NPDR
Homo sapiens (human)
DOID:3840
  • craniopharyngioma
  • Aliases:
    • neoplasm of Rathke's Pouch
Homo sapiens (human)
DOID:4297
  • scimitar syndrome
  • Aliases:
    • Halasz syndrome
    • congenital venolobar syndrome
    • hypogenetic lung syndrome
    • mirror-image lung syndrome
    • pulmonary venolobar syndrome
    • total anomalous pulmonary venous return
    • vena cava bronchovascular syndrome
Homo sapiens (human)
DOID:4202
  • brain stem glioma
  • Aliases:
    • Brainstem Neuroglial tumor
Homo sapiens (human)
DOID:12215
  • oligohydramnios
  • Aliases:
    • Oligohydramnios - delivered
    • antepartum oligohydramnios
    • delivered oligohydramnios
Homo sapiens (human)
DOID:0110375
  • retinitis pigmentosa 40
  • Aliases:
    • RP40
Homo sapiens (human)
DOID:0110863
  • congenital stationary night blindness autosomal dominant 2
  • Aliases:
    • CSNBAD2
    • Rambusch type congenital stationary night blindness
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: December 9, 2024