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 301 - 325 of 4621 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Organism
DOID:403
  • mouth disease
Homo sapiens (human)
DOID:431
  • myofascial pain syndrome
Homo sapiens (human)
DOID:14181
  • calcific tendinitis
Homo sapiens (human)
DOID:0050450
  • Gitelman syndrome
  • Aliases:
    • HYPOMAGNESEMIA-HYPOKALEMIA, PRIMARY RENOTUBULAR, WITH HYPOCALCIURIA
Homo sapiens (human)
DOID:4492
  • avian influenza
  • Aliases:
    • avian flu
    • bird flu
Homo sapiens (human)
DOID:6595
  • gastric tubular adenocarcinoma
  • Aliases:
    • tubular adenocarcinoma of stomach
Homo sapiens (human)
DOID:0060777
  • congenital secretory sodium diarrhea 8
  • Aliases:
    • DIAR8
Homo sapiens (human)
DOID:0060781
  • congenital secretory sodium diarrhea 3
  • Aliases:
    • congenital secretory sodium diarrhea 3 syndromic
    • congenital secretory sodium diarrhea 3 with or without other congenital anomalies
    • congenital secretory sodium diarrhoea 3
    • congenital secretory sodium diarrhoea 3 syndromic
    • congenital secretory sodium diarrhoea 3 with or without other congenital anomalies
Homo sapiens (human)
DOID:0111180
  • French Canadian Leigh disease
  • Aliases:
    • French Canadian type COX deficiency
    • French Canadian type Leigh syndrome
    • French Canadian type cytochrome c oxidase deficiency
    • Saguenay Lac saint Jean type COX deficiency
    • Saguenay Lac saint Jean type Leigh syndrome
    • mitochondrial complex IV deficiency nuclear type 5
Homo sapiens (human)
DOID:0050904
  • salivary gland carcinoma
Homo sapiens (human)
DOID:0111058
  • platelet-type bleeding disorder 12
  • Aliases:
    • BDPLT12
    • PGHS1 deficiency
    • platelet COX1 deficiency
    • platelet cyclooxygenase 1 deficiency
    • platelet prostaglandin-endoperoxide synthase 1 deficiency
Homo sapiens (human)
DOID:2825
  • nose disease
  • Aliases:
    • disorder of the nose
    • nasal disorder
Homo sapiens (human)
DOID:2965
  • bursitis
Homo sapiens (human)
DOID:14550
  • root resorption
Homo sapiens (human)
DOID:0111359
  • large congenital melanocytic nevus
  • Aliases:
    • Congenital pigmented nevus
    • GMN
    • Giant congenital melanocytic nevus
    • Giant pigmented hairy nevus
    • LCMN
Homo sapiens (human)
DOID:5567
  • ovarian germ cell teratoma
  • Aliases:
    • germ cell teratoma of Ovary
Homo sapiens (human)
DOID:6225
  • Cronkhite-Canada syndrome
  • Aliases:
    • gastric Cronkhite Canada polyposis
    • polyposis, skin pigmentation, alopecia, and fingernail changes
Homo sapiens (human)
DOID:6084
  • childhood ovarian germ cell tumor
  • Aliases:
    • paediatric Ovarian germ cell neoplasm
    • paediatric ovarian germ cell tumour
    • pediatric Ovarian germ cell neoplasm
    • pediatric ovarian germ cell tumor
Homo sapiens (human)
DOID:3001
  • female reproductive endometrioid cancer
  • Aliases:
    • endometrioid neoplasm
    • endometrioid tumor
Homo sapiens (human)
DOID:5830
  • cervical endometrioid adenocarcinoma
  • Aliases:
    • endometrioid carcinoma of the Cervix Uteri
Homo sapiens (human)
DOID:4586
  • familial meningioma
Homo sapiens (human)
DOID:4205
  • cerebellum cancer
  • Aliases:
    • cerebellar cancer
    • malignant tumor of Cerebellum
Homo sapiens (human)
DOID:7763
  • carcinoma of supraglottis
  • Aliases:
    • Supraglottic carcinoma
Homo sapiens (human)
DOID:264
  • hemangiopericytoma
  • Aliases:
    • Haemangiopericytic meningioma
    • hemangiopericytoma, malignant
    • malignant hemangiopericytoma
Homo sapiens (human)
DOID:5890
  • malignant adult ependymoma
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