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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 10801 - 10825 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Organism Source
DOID:3827
  • congenital diaphragmatic hernia
  • Aliases:
    • Diaphragmatic Hernia
Caenorhabditis elegans
DOID:3319
  • lymphangioleiomyomatosis
  • Aliases:
    • lung lymphangioleiomyomatosis
    • lymphangiomyomatosis
    • pulmonary lymphangioleiomyomatosis
Caenorhabditis elegans
DOID:0050827
  • rheumatic heart disease
  • Aliases:
    • rheumatic carditis
Caenorhabditis elegans
DOID:0080560
  • congenital disorder of glycosylation Ih
  • Aliases:
    • congenital disorder of glycosylation 1h
Caenorhabditis elegans
DOID:0050570
  • congenital disorder of glycosylation type I
Caenorhabditis elegans
DOID:0080575
  • Larsen-like syndrome B3GAT3 type
  • Aliases:
    • Larsen-like syndrome, B3GAT3 type
    • multiple joint dislocations-short stature-craniofacial dysmorphism-congenital heart defects syndrome
Caenorhabditis elegans
DOID:9206
  • Barrett's esophagus
  • Aliases:
    • Barrett esophagus
    • Barrett's esophagus with esophagitis
    • Barrett's oesophagus
    • Barrett's ulcer of esophagus
    • Barretts syndrome
    • ulcerative esophagitis
Caenorhabditis elegans
DOID:0112222
  • developmental and epileptic encephalopathy 88
  • Aliases:
    • DEE88
    • early infantile epileptic encephalopathy 88
Mus musculus (house mouse)
DOID:0080433
  • developmental and epileptic encephalopathy 51
  • Aliases:
    • DEE51
    • early infantile epileptic encephalopathy 51
Mus musculus (house mouse)
DOID:2962
  • Cockayne syndrome
  • Aliases:
    • Neill-Dingwall syndrome
Caenorhabditis elegans
DOID:0080907
  • Cockayne syndrome A
  • Aliases:
    • Cockayne syndrome type 1
    • Cockayne syndrome type I
Caenorhabditis elegans
DOID:0060240
  • UV-sensitive syndrome
Caenorhabditis elegans
DOID:0110969
  • brachydactyly type B1
  • Aliases:
    • BDB1
Caenorhabditis elegans
DOID:0080263
  • autosomal recessive nonsyndromic deafness 108
Caenorhabditis elegans
DOID:0060764
  • autosomal recessive Robinow syndrome
  • Aliases:
    • COVESDEM syndrome
    • RRS
    • costovertebral segmentation defect-mesomelia syndrome
Caenorhabditis elegans
DOID:674
  • cleft palate
  • Aliases:
    • Palatoschisis
Caenorhabditis elegans
DOID:11166
  • Human papillomavirus infectious disease
  • Aliases:
    • HPV
Caenorhabditis elegans
DOID:13949
  • interstitial cystitis
  • Aliases:
    • ulcerative cystitis
Caenorhabditis elegans
DOID:3457
  • invasive lobular carcinoma
  • Aliases:
    • Lobular carcinoma
    • Lobular carcinoma of breast
    • Lobular carcinoma of the breast
Caenorhabditis elegans
DOID:13133
  • HELLP syndrome
Caenorhabditis elegans
DOID:3443
  • mammary Paget's disease
  • Aliases:
    • Paget cell neoplasm
    • Paget's disease
    • Paget's disease of the breast
    • mammary Paget disease
Caenorhabditis elegans
DOID:62
  • aortic valve disease
Caenorhabditis elegans
DOID:571
  • median neuropathy
Caenorhabditis elegans
DOID:0060560
  • lethal congenital contracture syndrome 2
  • Aliases:
    • LCCS2
    • multiple contracture syndrome, Israeli-Bedouin type
Caenorhabditis elegans
DOID:0080679
  • neuronal intestinal dysplasia type A
Caenorhabditis elegans
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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