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 3326 - 3350 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲
DOID:0060712
  • autosomal recessive congenital ichthyosis 4A
  • Aliases:
    • ARCI4A
    • ICR2B
    • ichthyosis congenita IIB
    • lamellar ichthyosis 2
Homo sapiens (human)
DOID:1557
  • hypersensitivity reaction type III disease
  • Aliases:
    • immune complex disease
Homo sapiens (human)
DOID:2649
  • chondroblastoma
  • Aliases:
    • Chondroblastoma of bone
Homo sapiens (human)
DOID:13564
  • aspergillosis
  • Aliases:
    • Infection due to Aspergillus
Homo sapiens (human)
DOID:0110052
  • amelogenesis imperfecta type 1B
  • Aliases:
    • AI1B
    • AIH2
    • amelogenesis imperfecta type IB
    • autosomal dominant hypoplastic local amelogenesis imperfecta
    • hereditary localized enamel hypoplasia
Homo sapiens (human)
DOID:0090025
  • split hand-foot malformation 3
  • Aliases:
    • SHFM3
    • chromosome 10q24 duplication syndrome
    • distal limb deficiencies with micrognathia
Homo sapiens (human)
DOID:5075
  • myxopapillary ependymoma
Homo sapiens (human)
DOID:3500
  • gallbladder adenocarcinoma
  • Aliases:
    • adenocarcinoma of the gallbladder
Homo sapiens (human)
DOID:6128
  • gliomatosis cerebri
  • Aliases:
    • Astrocytosis cerebri
Homo sapiens (human)
DOID:0110389
  • retinitis pigmentosa 73
  • Aliases:
    • RP73
Homo sapiens (human)
DOID:4258
  • Weissenbacher-Zweymuller syndrome
  • Aliases:
    • Piere-Robin syndrome
    • Pierre Robin Malformation
Homo sapiens (human)
DOID:1729
  • retinal vascular occlusion
  • Aliases:
    • Retinal vasc. occlusion
Homo sapiens (human)
DOID:9273
  • citrullinemia
  • Aliases:
    • ASS deficiency
    • deficiency of citrulline-aspartate ligase
Homo sapiens (human)
DOID:2384
  • Wernicke encephalopathy
  • Aliases:
    • Wernicke's disease
    • Wernicke's encephalopathy
Homo sapiens (human)
DOID:0050853
  • chronic venous insufficiency
Homo sapiens (human)
DOID:0110719
  • Warburg micro syndrome 4
  • Aliases:
    • Micro Syndrome 4
    • WARBM4
Homo sapiens (human)
DOID:0060839
  • isolated microphthalmia 2
  • Aliases:
    • MCOP2
Homo sapiens (human)
DOID:0112282
  • spondyloepiphyseal dysplasia Kimberley type
  • Aliases:
    • SEDK
Homo sapiens (human)
DOID:4450
  • renal cell carcinoma
  • Aliases:
    • RCC
    • adenocarcinoma of kidney
    • hypernephroma
Homo sapiens (human)
DOID:2568
  • cervicitis
Homo sapiens (human)
DOID:4767
  • classic pulmonary blastoma
Homo sapiens (human)
DOID:1837
  • diabetic ketoacidosis
  • Aliases:
    • DIABETES MELLITUS, KETOSIS-PRONE
    • ketosis-prone diabetes mellitus
Homo sapiens (human)
DOID:6712
  • anterior spinal artery syndrome
  • Aliases:
    • Anterior spinal artery occlusion syndrome
Homo sapiens (human)
DOID:4607
  • biliary tract cancer
  • Aliases:
    • malignant tumour of biliary tract
Homo sapiens (human)
DOID:8125
  • osteochondrosis
  • Aliases:
    • Epiphyseal necrosis
    • apophysitis
    • epiphysitis
    • osteochondritis
    • osteochondritis juvenilis
Homo sapiens (human)

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

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