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 3976 - 4000 of 4621 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲
DOID:4889
  • lymph node tuberculosis
  • Aliases:
    • Tuberculous adenitis
    • Tuberculous lymphadenopathy
    • king's evil
    • scrofula
Homo sapiens (human)
DOID:0060782
  • EEC syndrome
  • Aliases:
    • Rudiger syndrome 1
    • Walker-Clodius syndrome
    • ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome
    • ectrodactyly-ectodermal dysplasia-clefting syndrome
Homo sapiens (human)
DOID:11722
  • myotonic dystrophy type 1
  • Aliases:
    • Dystrophia myotonica
    • Steinert disease
    • congenital myotonic dystrophy
    • myotonic dystrophy of Steinert
Homo sapiens (human)
DOID:0110916
  • hereditary spherocytosis type 1
  • Aliases:
    • HS1
    • SPH1
    • hereditary spherocytosis 1
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
Homo sapiens (human)
DOID:4784
  • immune-complex glomerulonephritis
  • Aliases:
    • Immune Complex Glomerulonephritis
Homo sapiens (human)
DOID:701
  • dentin dysplasia
  • Aliases:
    • Dentinal dysplasia
Homo sapiens (human)
DOID:0110283
  • autosomal recessive limb-girdle muscular dystrophy type 2J
  • Aliases:
    • LGMD2J
    • muscular dystrophy, limb-girdle, type 2J
Homo sapiens (human)
DOID:0080001
  • bone disease
Homo sapiens (human)
DOID:10930
  • borderline personality disorder
Homo sapiens (human)
DOID:0080844
  • omodysplasia 1
Homo sapiens (human)
DOID:4562
  • subacute bacterial endocarditis
  • Aliases:
    • Endocarditis lenta
    • SBE - Subacute bacterial endocarditis
    • Subacute endocarditis, lenta
Homo sapiens (human)
DOID:1679
  • cystitis
Homo sapiens (human)
DOID:11256
  • typhus
  • Aliases:
    • Endemic Typhus fever
    • Exanthematic Typhus fever
    • Flea typhus
    • Louse-borne [epidemic] typhus
    • Moscow typhus
    • Murine [endemic] typhus
    • Typhus fever
    • endemic flea-borne typhus
    • epidemic louse-borne typhus
Homo sapiens (human)
DOID:3606
  • ovarian mucinous adenocarcinoma
  • Aliases:
    • mucinous carcinoma of Ovary
Homo sapiens (human)
DOID:930
  • orbital disease
Homo sapiens (human)
DOID:962
  • neurofibroma
Homo sapiens (human)
DOID:0090064
  • familial cold autoinflammatory syndrome 3
Homo sapiens (human)
DOID:4271
  • microsporidiosis
  • Aliases:
    • Infection by Microspora
    • Infection by Microsporea
    • Infection by Microsporida
Homo sapiens (human)
DOID:12382
  • complex partial epilepsy
  • Aliases:
    • Complex partial epileptic seizure
    • epilepsy, psychomotor
    • psychomotor epilepsy
Homo sapiens (human)
DOID:12978
  • Plasmodium vivax malaria
  • Aliases:
    • Malaria by Plasmodium vivax
    • Vivax Malaria
Homo sapiens (human)
DOID:0050145
  • adenoiditis
  • Aliases:
    • chronic adenoiditis
Homo sapiens (human)
DOID:12801
  • mucopolysaccharidosis III
  • Aliases:
    • Mucopolysaccharidosis, MPS-III
    • N-sulphoglucosamine sulphohydrolase deficiency
    • Sanfilippo's syndrome
    • heparan sulfate sulfatase deficiency
Homo sapiens (human)
DOID:12466
  • secondary hyperparathyroidism
Homo sapiens (human)
DOID:0050647
  • Arts syndrome
  • Aliases:
    • ARTS
    • Lethal ataxia with deafness and optic atrophy
    • MRXS18
    • MRXSARTS
    • fatal X-linked ataxia with deafness and loss of vision
    • syndromic X-linked mental retardation 18
    • syndromic X-linked mental retardation Arts type
Homo sapiens (human)

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Last updated: August 19, 2024