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 9351 - 9375 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:1227
  • neutropenia
Homo sapiens (human)
DOID:0050419
  • complement factor I deficiency
  • Aliases:
    • C3 INACTIVATOR DEFICIENCY
    • COMPLEMENT COMPONENT 3 INACTIVATOR DEFICIENCY
Rattus norvegicus (Norway rat)
DOID:0111322
  • idiopathic generalized epilepsy 8
  • Aliases:
    • EIG8
Rattus norvegicus (Norway rat)
DOID:0060738
  • junctional epidermolysis bullosa non-Herlitz type
  • Aliases:
    • GABEB
    • JEB-nH gen
    • JEN-nH
    • generalized atrophic benign epidermolysis bullosa
    • generalized junctional epidermolysis bullosa, non-Herlitz type
    • junctional epidermolysis bullosa generalisata mitis
    • junctional epidermolysis bullosa, Disentis type
Mus musculus (house mouse)
DOID:9620
  • vesicoureteral reflux
  • Aliases:
    • vesico-ureteral reflux
Caenorhabditis elegans
DOID:0112378
  • muscular dystrophy-dystroglycanopathy type B3
  • Aliases:
    • MDDGB3
    • congenital muscular dystrophy POMGNT1-related
Xenopus tropicalis (tropical clawed frog)
DOID:0070537
  • spastic tetraplegia, thin corpus callosum, and progressive microcephaly
  • Aliases:
    • SPATCCM
Mus musculus (house mouse)
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:0081292
  • traumatic brain injury
Homo sapiens (human)
DOID:0050787
  • juvenile polyposis syndrome
Homo sapiens (human)
DOID:526
  • human immunodeficiency virus infectious disease
  • Aliases:
    • HIV infection
Homo sapiens (human)
DOID:0050540
  • Charcot-Marie-Tooth disease type 3
  • Aliases:
    • DEJERINE-SOTTAS NEUROPATHY
    • DEJERINE-SOTTAS SYNDROME
Xenopus tropicalis (tropical clawed frog)
DOID:0040089
  • autoimmune optic neuritis
Homo sapiens (human)
DOID:0110497
  • autosomal recessive nonsyndromic deafness 39
  • Aliases:
    • DFNB39
    • autosomal recessive deafness 39
Homo sapiens (human)
DOID:0111347
  • epidermolysis bullosa with congenital localized absence of skin and deformity of nails
  • Aliases:
    • EBD, Bart type
    • epidermolysis bullosa dystrophica, Bart type
Homo sapiens (human)
DOID:0110584
  • autosomal dominant nonsyndromic deafness 6
  • Aliases:
    • DFNA14
    • DFNA38
    • DFNA6
    • autosomal dominant deafness 14
    • autosomal dominant deafness 38
    • autosomal dominant deafness 6
Drosophila melanogaster (fruit fly)
DOID:2215
  • factor VII deficiency
  • Aliases:
    • deficiency, stable
Rattus norvegicus (Norway rat)
DOID:9470
  • bacterial meningitis
Drosophila melanogaster (fruit fly)
DOID:1037
  • lymphoid leukemia
  • Aliases:
    • lymphoblastic leukaemia
    • lymphoblastic leukemia
    • lymphocytic leukaemia
Saccharomyces cerevisiae S288C
DOID:0111160
  • camptodactyly-tall stature-scoliosis-hearing loss syndrome
  • Aliases:
    • CATSHL syndrome
Homo sapiens (human)
DOID:3159
  • photosensitivity disease
  • Aliases:
    • Photodermatitis
Drosophila melanogaster (fruit fly)
DOID:12705
  • Friedreich ataxia
  • Aliases:
    • Friedreich's ataxia
    • Friedreich's tabes
Xenopus laevis (African clawed frog)
DOID:0111330
  • combined saposin deficiency
  • Aliases:
    • PSAPD
    • combined SAP deficiency
    • encephalopathy due to prosaposin deficiency
Rattus norvegicus (Norway rat)
DOID:289
  • endometriosis
Danio rerio (zebrafish)
DOID:0060303
  • complement component 9 deficiency
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: December 9, 2024