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 1326 - 1350 of 4621 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism
DOID:0060395
  • chromosome 15q24 deletion syndrome
  • Aliases:
    • 15q24 microdeletion syndrome
Homo sapiens (human)
DOID:0060768
  • Smith-Magenis syndrome
  • Aliases:
    • 17p11.2 microdeletion syndrome
    • chromosome 17p11.2 deletion syndrome
Homo sapiens (human)
DOID:3463
  • breast disease
Homo sapiens (human)
DOID:10686
  • lactocele
  • Aliases:
    • Galactocele
Homo sapiens (human)
DOID:0070189
  • X-linked spermatogenic failure 1
  • Aliases:
    • SPGFX1
Homo sapiens (human)
DOID:10688
  • hypertrophy of breast
  • Aliases:
    • breasts enlarged
    • large breast
Homo sapiens (human)
DOID:11603
  • infant gynecomastia
  • Aliases:
    • Neonatal gynaecomastia
    • breast engorgement in newborn
Homo sapiens (human)
DOID:12698
  • gynecomastia
Homo sapiens (human)
DOID:0060076
  • estrogen-receptor negative breast cancer
Homo sapiens (human)
DOID:8704
  • genital herpes
  • Aliases:
    • Genital herpes simplex
    • Herpes Genitalis
    • Virus-Genital Herpes
    • venereal herpes
Homo sapiens (human)
DOID:0080523
  • adult-onset leukoencephalopathy with axonal spheroids and pigmented glia
  • Aliases:
    • hereditary diffuse leukoencephalopathy with spheroids
Homo sapiens (human)
DOID:0080540
  • galactosialidosis
Homo sapiens (human)
DOID:0111392
  • mucopolysaccharidosis type IVB
  • Aliases:
    • MPS IVB
    • MPS4B
    • Morquio disease type B
    • Morquio syndrome B
    • beta-D-galactosidase deficiency
    • mucopolysaccharidosis type IVB (Morquio)
Homo sapiens (human)
DOID:13945
  • CADASIL
  • Aliases:
    • cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
    • hereditary multi-infarct dementia
Homo sapiens (human)
DOID:0111035
  • CADASIL 1
  • Aliases:
    • autosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy type 1
Homo sapiens (human)
DOID:5684
  • spondyloepimetaphyseal dysplasia, Sponastrime type
  • Aliases:
    • Spondylar and nasal Alterations-Striated Metaphyses syndrome
    • sponastrime dysplasia
Homo sapiens (human)
DOID:0060345
  • bacillary angiomatosis
Homo sapiens (human)
DOID:11104
  • spotted fever
  • Aliases:
    • Spotted fever group rickettsial disease
Homo sapiens (human)
DOID:11103
  • rickettsialpox
  • Aliases:
    • Rickettsia akari spotted fever
    • Vesicular rickettsiosis
Homo sapiens (human)
DOID:11254
  • Brill-Zinsser disease
  • Aliases:
    • Brill Zinsser disease
    • Brill's disease
    • Recrudescent typhus
Homo sapiens (human)
DOID:10921
  • Siberian tick typhus
  • Aliases:
    • North Asian tick fever
    • North Asian tick typhus
    • Rickettsia sibirica spotted fever
    • manchurian typhus
Homo sapiens (human)
DOID:0050852
  • limb ischemia
Homo sapiens (human)
DOID:0080307
  • myofibrillar myopathy
Homo sapiens (human)
DOID:12961
  • Poland syndrome
  • Aliases:
    • Poland's syndactyly
Homo sapiens (human)
DOID:11126
  • acquired thrombocytopenia
  • Aliases:
    • secondary thrombocytopenia
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