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 July 29, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 3801 - 3825 of 4621 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism
DOID:0090078
  • hypogonadotropic hypogonadism 7 with or without anosmia
Homo sapiens (human)
DOID:6193
  • epithelioid sarcoma
  • Aliases:
    • epithelioid cell sarcoma
Homo sapiens (human)
DOID:4235
  • spindle cell sarcoma
Homo sapiens (human)
DOID:1115
  • sarcoma
  • Aliases:
    • connective and soft tissue neoplasm
    • tumor of soft tissue and skeleton
Homo sapiens (human)
DOID:0090004
  • progressive pseudorheumatoid arthropathy of childhood
  • Aliases:
    • spondyloepiphyseal dysplasia tarda-progressive arthropathy syndrome
Homo sapiens (human)
DOID:2964
  • periarthritis
Homo sapiens (human)
DOID:203
  • exostosis
  • Aliases:
    • bone spur
    • bony outgrowth
    • orbital exostosis
    • osteophyte
    • swimmer's exostosis
Homo sapiens (human)
DOID:813
  • septic arthritis
  • Aliases:
    • infectious arthritis
Homo sapiens (human)
DOID:12721
  • multiple epiphyseal dysplasia
  • Aliases:
    • polyepiphyseal dysplasia
Homo sapiens (human)
DOID:2256
  • osteochondrodysplasia
  • Aliases:
    • Cartilage Development disorder
    • Congenital anomaly of cartilage
    • Osteochondrodysplasia syndrome
    • chondrodystrophy
    • skeletal dysplasia
Homo sapiens (human)
DOID:9521
  • Laron syndrome
  • Aliases:
    • Laron-type isolated somatotropin defect
Homo sapiens (human)
DOID:4480
  • achondroplasia
  • Aliases:
    • Achondroplastic physique
    • Chondrodystrophia
    • osteosclerosis congenita
Homo sapiens (human)
DOID:12169
  • carpal tunnel syndrome
  • Aliases:
    • CTS - Carpal tunnel syndrome
    • Median nerve entrapment
    • carpal tunnel median neuropathy
Homo sapiens (human)
DOID:10324
  • anthracosilicosis
Homo sapiens (human)
DOID:10320
  • asbestosis
Homo sapiens (human)
DOID:0080332
  • bicuspid aortic valve disease
  • Aliases:
    • Familial bicuspid aortic valve
Homo sapiens (human)
DOID:0080333
  • aortic valve disease 1
Homo sapiens (human)
DOID:5688
  • Werner syndrome
  • Aliases:
    • WS
    • Werner's syndrome
    • adult premature ageing syndrome
    • adult progeria
Homo sapiens (human)
DOID:3911
  • progeria
  • Aliases:
    • HGPS
    • Hutchinson Gilford syndrome
    • Hutchinson-Gilford Progeria syndrome
    • Hutchinson-Gilford disease
Homo sapiens (human)
DOID:0080334
  • aortic valve disease 2
Homo sapiens (human)
DOID:1712
  • aortic valve stenosis
  • Aliases:
    • Aortic stenosis
    • Rheumatic aortic stenosis
    • rheumatic aortic valve stenosis
Homo sapiens (human)
DOID:2247
  • spondylosis
  • Aliases:
    • Lumbar spondylosis with myelopathy
    • Spondylogenic compression of lumbar spinal cord
    • Spondylogenic compression of thoracic spinal cord
    • Thoracic or lumbar spondylosis with myelopathy
    • lumbosacral spondylosis without myelopathy
    • spondylosis with myelopathy
Homo sapiens (human)
DOID:1123
  • spondyloarthropathy
  • Aliases:
    • spondarthropathy
    • spondylarthrosis
Homo sapiens (human)
DOID:0080001
  • bone disease
Homo sapiens (human)
DOID:1222
  • cartilage disease
  • Aliases:
    • Cartilage disorder
    • Chondropathy
Homo sapiens (human)

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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: August 19, 2024