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 751 - 775 of 4621 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼
DOID:0060184
  • lymphocytic colitis
Homo sapiens (human)
DOID:11130
  • secondary hypertension
Homo sapiens (human)
DOID:4676
  • uremia
  • Aliases:
    • UREMIA OF renal ORIGIN
Homo sapiens (human)
DOID:7475
  • diverticulitis
Homo sapiens (human)
DOID:11105
  • fundus albipunctatus
  • Aliases:
    • Pigmentary retinal dystrophy
    • retinitis punctata albescens
Homo sapiens (human)
DOID:4202
  • brain stem glioma
  • Aliases:
    • Brainstem Neuroglial tumor
Homo sapiens (human)
DOID:0080146
  • childhood B-cell acute lymphoblastic leukemia
Homo sapiens (human)
DOID:11613
  • hyperandrogenism
  • Aliases:
    • hyperandrogenization syndrome
Homo sapiens (human)
DOID:3071
  • gliosarcoma
  • Aliases:
    • Glioblastoma with sarcomatous component
Homo sapiens (human)
DOID:3755
  • antithrombin III deficiency
  • Aliases:
    • AT III deficiency
    • hereditary thrombophilia due to congenital antithrombin deficiency
Homo sapiens (human)
DOID:0112216
  • developmental and epileptic encephalopathy 80
  • Aliases:
    • DEE80
    • GPIBD20
    • early infantile epileptic encephalopathy 80
    • glycosylphosphatidylinositol biosynthesis defect 20
Homo sapiens (human)
DOID:9649
  • congenital nystagmus
Homo sapiens (human)
DOID:0060699
  • familial hypocalciuric hypercalcemia
  • Aliases:
    • FBH
    • FBHH
    • FHH
    • familial benign hypercalcemia
    • familial benign hypocalciuric hypercalcemia
Homo sapiens (human)
DOID:0112379
  • muscular dystrophy-dystroglycanopathy type B4
  • Aliases:
    • MDDGB4
    • congenital muscular dystrophy FKTN-related
Homo sapiens (human)
DOID:5732
  • pyosalpinx
  • Aliases:
    • Pyosalpingitis
Homo sapiens (human)
DOID:0111128
  • focal segmental glomerulosclerosis 1
  • Aliases:
    • FSGS1
Homo sapiens (human)
DOID:1697
  • ichthyosis
  • Aliases:
    • ichthyoses
    • non-syndromic ichthyosis
Homo sapiens (human)
DOID:0080218
  • primary spontaneous pneumothorax
Homo sapiens (human)
DOID:0111231
  • congenital muscular dystrophy-dystroglycanopathy type A8
  • Aliases:
    • MDDGA8
    • Walker-Warburg syndrome or muscle-eye-brain disease GTDC2-related
    • congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A8
Homo sapiens (human)
DOID:5418
  • schizoaffective disorder
Homo sapiens (human)
DOID:0060742
  • methylmalonic acidemia cblA type
  • Aliases:
    • methylmalonic aciduria cblA type
    • methylmalonic aciduria, vitamin B12-responsive due to a defect in synthesis of adenosylcobalamin cb1A type
Homo sapiens (human)
DOID:626
  • complement deficiency
  • Aliases:
    • Complement deficiency disease
Homo sapiens (human)
DOID:0060218
  • CREST syndrome
Homo sapiens (human)
DOID:4998
  • trichorhinophalangeal syndrome type II
  • Aliases:
    • Langer-Giedion syndrome
    • Trichorhinophalangeal dysplasia type II
    • trichorhinophalangeal syndrome type 2
Homo sapiens (human)
DOID:4586
  • familial meningioma
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