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 4001 - 4025 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:8692
  • myeloid leukemia
  • Aliases:
    • Non-Lymphocytic Leukemia
    • leukaemia myelogenous
    • leukemia myelogenous
    • myeloid granulocytic leukaemia
    • myeloid granulocytic leukemia
    • myeloid leukaemia
Danio rerio (zebrafish)
DOID:0080096
  • myofibrillar myopathy 5
  • Aliases:
    • filaminopathy
Homo sapiens (human)
DOID:0110344
  • osteogenesis imperfecta type 5
  • Aliases:
    • OI5
    • osteogenesis imperfecta type V
Homo sapiens (human)
DOID:0070286
  • primary autosomal recessive microcephaly 3
  • Aliases:
    • MCPH3
Homo sapiens (human)
DOID:10123
  • pigmentation disease
Caenorhabditis elegans
DOID:1725
  • peritoneum cancer
Homo sapiens (human)
DOID:0110862
  • congenital stationary night blindness autosomal dominant 1
  • Aliases:
    • CSNBAD1
    • rhodopsin-related congenital stationary night blindness
Homo sapiens (human)
DOID:7998
  • hyperthyroidism
  • Aliases:
    • overactive thyroid
Mus musculus (house mouse)
DOID:10487
  • Hirschsprung's disease
  • Aliases:
    • Hirschsprung disease
    • aganglionic megacolon
    • congenital megacolon
    • macrocolon
    • pelvirectal achalasia
    • total intestinal aganglionosis
Drosophila melanogaster (fruit fly)
DOID:11054
  • urinary bladder cancer
  • Aliases:
    • bladder cancer
    • tumor of the bladder
Caenorhabditis elegans
DOID:13088
  • periventricular leukomalacia
Rattus norvegicus (Norway rat)
DOID:0080559
  • congenital disorder of glycosylation Ig
  • Aliases:
    • ALG12-congenital disorder of glycosylation
    • congenital disorder of glycosylation 1g
Xenopus tropicalis (tropical clawed frog)
DOID:0111903
  • thrombophilia due to HRG deficiency
  • Aliases:
    • THPH11
    • hereditary thrombophilia due to congenital HRG deficiency
    • hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency
Homo sapiens (human)
DOID:8506
  • bullous pemphigoid
Mus musculus (house mouse)
DOID:3209
  • junctional epidermolysis bullosa
  • Aliases:
    • congenital junctional epidermolysis bullosa
Homo sapiens (human)
DOID:374
  • nutrition disease
  • Aliases:
    • Nutritional disorder
Rattus norvegicus (Norway rat)
DOID:0070526
  • PLACK syndrome
  • Aliases:
    • peeling skin with leukonychia, acral punctate keratoses, cheilitis, and knuckle pads
Homo sapiens (human)
DOID:10283
  • prostate cancer
  • Aliases:
    • NGP - new growth of prostate
    • hereditary prostate cancer
    • malignant tumor of the prostate
    • prostate cancer, familial
    • prostate neoplasm
    • prostatic cancer
    • prostatic neoplasm
    • tumor of the prostate
Homo sapiens (human)
DOID:2377
  • multiple sclerosis
  • Aliases:
    • Generalized multiple sclerosis
    • insular sclerosis
Rattus norvegicus (Norway rat)
DOID:635
  • acquired immunodeficiency syndrome
  • Aliases:
    • AIDS
    • acquired Immune deficiency
Rattus norvegicus (Norway rat)
DOID:2377
  • multiple sclerosis
  • Aliases:
    • Generalized multiple sclerosis
    • insular sclerosis
Danio rerio (zebrafish)
DOID:0070128
  • congenital nongoitrous hypothyroidism 6
  • Aliases:
    • CHNG6
Homo sapiens (human)
DOID:10024
  • migraine with aura
  • Aliases:
    • classic migraine
Homo sapiens (human)
DOID:11836
  • clubfoot
  • Aliases:
    • Congenital equinovarus
    • Equinovarus deformity of foot
    • congenital clubfoot
    • congenital talipes equinovarus
Rattus norvegicus (Norway rat)
DOID:850
  • lung disease
Xenopus laevis (African clawed frog)

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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