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 3951 - 3975 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼
DOID:0060841
  • isolated microphthalmia 8
  • Aliases:
    • MCOP8
Homo sapiens (human)
DOID:9602
  • necrotizing fasciitis
Homo sapiens (human)
DOID:4448
  • macular degeneration
  • Aliases:
    • Macular degeneration of retina
Homo sapiens (human)
DOID:1679
  • cystitis
Homo sapiens (human)
DOID:230
  • lateral sclerosis
  • Aliases:
    • adult-onset primary lateral sclerosis
    • primary lateral sclerosis
Homo sapiens (human)
DOID:9352
  • type 2 diabetes mellitus
  • Aliases:
    • NIDDM
    • insulin resistance
    • non-insulin-dependent diabetes mellitus
    • type 2 diabetes
    • type II diabetes mellitus
Homo sapiens (human)
DOID:0110570
  • autosomal dominant nonsyndromic deafness 47
  • Aliases:
    • DFNA47
    • autosomal dominant deafness 47
Homo sapiens (human)
DOID:0050523
  • adult T-cell leukemia/lymphoma
  • Aliases:
    • Adult T-cell leukemia/lymphoma (HTLV-1 positive)
    • adult T-cell leukemia
Homo sapiens (human)
DOID:13620
  • patent foramen ovale
  • Aliases:
    • Atrial septal defect within oval fossa
    • Defect, Patent or persistent, ostium secundum
    • Ostium secundum type atrial septal defect
    • Persistent ostium secundum
    • foramen ovale patent
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:4702
  • mongolian spot
  • Aliases:
    • Mongolian Macula
Homo sapiens (human)
DOID:13269
  • hereditary coproporphyria
  • Aliases:
    • Coproporphyrinogen oxidase deficiency
    • hereditary coproporphyria porphyria
Homo sapiens (human)
DOID:0060294
  • cold-induced sweating syndrome
  • Aliases:
    • Crisponi syndrome
    • Sohar-Crisponi syndrome
Homo sapiens (human)
DOID:0060697
  • hyperekplexia 2
  • Aliases:
    • HKPX2
Homo sapiens (human)
DOID:0110881
  • holoprosencephaly 1
  • Aliases:
    • HPE1
Homo sapiens (human)
DOID:3039
  • cecum adenocarcinoma
  • Aliases:
    • Cecal adenocarcinoma
Homo sapiens (human)
DOID:0050453
  • lissencephaly
Homo sapiens (human)
DOID:2712
  • phimosis
  • Aliases:
    • Tight foreskin
    • Tight frenulum
Homo sapiens (human)
DOID:0060791
  • hypomyelinating leukodystrophy 9
  • Aliases:
    • HLD9
    • RARS-related autosomal recessive hypomyelinating leukodystrophy
Homo sapiens (human)
DOID:8805
  • intermediate coronary syndrome
  • Aliases:
    • Angina at rest
    • Anginal chest pain at rest
    • Impending infarction
    • Preinfarction angina
    • Unstable angina
    • Worsening angina
Homo sapiens (human)
DOID:3275
  • thymoma
Homo sapiens (human)
DOID:0110220
  • Brugada syndrome 3
  • Aliases:
    • BRGDA3
Homo sapiens (human)
DOID:0050429
  • Hailey-Hailey disease
  • Aliases:
    • BENIGN CHRONIC PEMPHIGUS
    • Pemphigus, Benign Familial
Homo sapiens (human)
DOID:0111132
  • focal segmental glomerulosclerosis 7
  • Aliases:
    • FSGS7
Homo sapiens (human)
DOID:3459
  • breast carcinoma
  • Aliases:
    • Mammary carcinoma
    • carcinoma of breast
Homo sapiens (human)

About Release Notes Help Feedback

Click here to visit the beta site.


International Collaboration

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


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.0.0

Last updated: August 19, 2024