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:1911
  • endodermal sinus tumor
  • Aliases:
    • Hepatoid yolk sac tumour
    • Yolk Sac neoplasm
    • Yolk sac tumour
    • endodermal sinus tumour
    • infantile embryonal carcinoma
    • yolk sac tumor
Homo sapiens (human)
DOID:2339
  • Crouzon syndrome
  • Aliases:
    • Craniofacial Dysostosis
Homo sapiens (human)
DOID:4773
  • congenital mesoblastic nephroma
Homo sapiens (human)
DOID:5348
  • adult endodermal sinus tumor
  • Aliases:
    • adult Yolk Sac neoplasm
    • adult endodermal sinus neoplasm
Homo sapiens (human)
DOID:5299
  • endometrial clear cell adenocarcinoma
  • Aliases:
    • Clear cell carcinoma of Endometrium
Homo sapiens (human)
DOID:5681
  • ovarian embryonal carcinoma
  • Aliases:
    • Embryonal carcinoma of ovary
    • Embryonal carcinoma of the Ovary
Homo sapiens (human)
DOID:4772
  • obsolete mesoblastic nephroma
Homo sapiens (human)
DOID:3596
  • placental site trophoblastic tumor
  • Aliases:
    • Placental-Site Gestational Trophoblastic neoplasm
    • placental site trophoblastic tumour
Homo sapiens (human)
DOID:0080844
  • omodysplasia 1
Homo sapiens (human)
DOID:2951
  • motion sickness
  • Aliases:
    • Travel Sickness
Homo sapiens (human)
DOID:4372
  • intracranial embolism
  • Aliases:
    • Cerebral embolism with cerebral infarction
    • cerebral embolism
Homo sapiens (human)
DOID:0060802
  • syndromic X-linked intellectual disability Snyder type
  • Aliases:
    • SRS
    • Snyder-Robinson mental retardation syndrome
    • Snyder-Robinson syndrome
    • mental retardation, X-linked, Snyder-Robinson type
    • spermine synthase deficiency
Homo sapiens (human)
DOID:0050888
  • syndromic intellectual disability
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:0080932
  • primary localized cutaneous amyloidosis 3
  • Aliases:
    • Amyloidosis cutis dyschromica
Homo sapiens (human)
DOID:11758
  • iron deficiency anemia
Homo sapiens (human)
DOID:0070004
  • myeloid neoplasm
Homo sapiens (human)
DOID:7941
  • Barrett's adenocarcinoma
  • Aliases:
    • Barrett adenocarcinoma
    • adenocarcinoma Arising in Barrett's Mucosa
Homo sapiens (human)
DOID:14701
  • propionic acidemia
  • Aliases:
    • GLYCINEMIA, KETOTIC
    • KETOTIC HYPERGLYCINEMIA
    • ketotic II glycinemia
    • ketotic glycinemia
    • propionic aciduria
    • propionyl-CoA carboxylase deficiency
Homo sapiens (human)
DOID:3572
  • intracranial sinus thrombosis
Homo sapiens (human)
DOID:0080797
  • nasal type extranodal NK/T-cell lymphoma
Homo sapiens (human)
DOID:10590
  • mild pre-eclampsia
Homo sapiens (human)
DOID:0111671
  • primary hyperoxaluria type 2
  • Aliases:
    • D-glycerate dehydrogenase deficiency
    • HP2
    • L-glyceric aciduria
    • glyoxylate reductase/hydroxypyruvate reductase deficiency
    • oxalosis II
Homo sapiens (human)
DOID:0050850
  • diabetic encephalopathy
Homo sapiens (human)
DOID:12803
  • Sly syndrome
  • Aliases:
    • MPS VII - Sly syndrome
    • beta-glucuronidase deficiency
    • deficiency of beta-glucuronidase
    • mucopolysaccharidosis VII
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