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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 4751 - 4775 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:255
  • hemangioma
Caenorhabditis elegans
DOID:0050591
  • tooth agenesis
  • Aliases:
    • familial tooth agenesis
    • hypodontia
    • oligodontia
    • selective tooth agenesis
Xenopus laevis (African clawed frog)
DOID:10609
  • rickets
  • Aliases:
    • active rickets
Homo sapiens (human)
DOID:4195
  • hyperglycemia
Xenopus tropicalis (tropical clawed frog)
DOID:0060162
  • dentatorubral-pallidoluysian atrophy
  • Aliases:
    • DRPLA
    • Haw River Syndrome
    • Naito-Oyanagi disease
Mus musculus (house mouse)
DOID:0110861
  • autosomal recessive polycystic kidney disease
  • Aliases:
    • Arpkd
    • Pkhd1
    • Polycystic Kidney Disease, Infantile, Type I
    • Polycystic Kidney and Hepatic Disease 1
Caenorhabditis elegans
DOID:12803
  • Sly syndrome
  • Aliases:
    • MPS VII - Sly syndrome
    • beta-glucuronidase deficiency
    • deficiency of beta-glucuronidase
    • mucopolysaccharidosis VII
Rattus norvegicus (Norway rat)
DOID:0050547
  • familial medullary thyroid carcinoma
  • Aliases:
    • THYROID CARCINOMA, FAMILIAL MEDULLARY
Mus musculus (house mouse)
DOID:11996
  • spermatic cord torsion
  • Aliases:
    • Torsion of testicle
    • Torsion of testis
    • testicular Torsion
Homo sapiens (human)
DOID:0111955
  • immunodeficiency 27A
  • Aliases:
    • IMD27A
    • autosomal recessive IFNGR1 deficiency
    • autosomal recessive MSMD due to partial IFNgammaR1 deficiency
    • autosomal recessive MSMD due to partial interferon gamma receptor 1 deficiency
    • autosomal recessive immunodeficiency 27A, mycobacteriosis
    • autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency
    • autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial interferon gamma receptor 1 deficiency
Homo sapiens (human)
DOID:0111938
  • immunodeficiency 24
  • Aliases:
    • IMD24
    • SCID due to CTPS1 deficiency
    • severe combined immunodeficiency due to CTPS1 deficiency
Homo sapiens (human)
DOID:5031
  • adult pineal parenchymal tumor
  • Aliases:
    • adult Pineal Parenchymal neoplasm
Homo sapiens (human)
DOID:2055
  • post-traumatic stress disorder
  • Aliases:
    • PTSD
    • traumatic neurosis
Mus musculus (house mouse)
DOID:4480
  • achondroplasia
  • Aliases:
    • Achondroplastic physique
    • Chondrodystrophia
    • osteosclerosis congenita
Drosophila melanogaster (fruit fly)
DOID:2384
  • Wernicke encephalopathy
  • Aliases:
    • Wernicke's disease
    • Wernicke's encephalopathy
Homo sapiens (human)
DOID:0070029
  • ITM2B-related cerebral amyloid angiopathy 1
  • Aliases:
    • Cerebral Amyloid Angiopathy, British Type
    • FBD
    • Familial British Dementia
    • Presenile Dementia with Spastic Ataxia
Rattus norvegicus (Norway rat)
DOID:2871
  • endometrial carcinoma
  • Aliases:
    • carcinoma of the Endometrium
    • endometrioid carcinoma
    • endometrioid carcinoma of female Reproductive system
Caenorhabditis elegans
DOID:0070043
  • autosomal dominant intellectual developmental disorder 13
  • Aliases:
    • MRD13
    • autosomal dominant mental retardation 13
    • autosomal dominant non-syndromic intellectual disability 13
    • mental retardation, autosomal dominant 13, with neuronal migration defects
Homo sapiens (human)
DOID:0081292
  • traumatic brain injury
Mus musculus (house mouse)
DOID:0112221
  • developmental and epileptic encephalopathy 87
  • Aliases:
    • DEE87
    • early infantile epileptic encephalopathy 87
Mus musculus (house mouse)
DOID:0111181
  • familial hemiplegic migraine 1
  • Aliases:
    • FHM1
    • MHP1
    • familial hemiplegic migraine1 with progressive cerebellar ataxia
Drosophila melanogaster (fruit fly)
DOID:8991
  • cervix uteri carcinoma in situ
  • Aliases:
    • CIN III
    • CIN III - carcinoma in situ of cervix
    • CIN III - severe dyskaryosis
    • Cervix Ca in situ
    • Severe Dysplasia of the Cervix Uteri
    • Severe dysplasia of cervix
    • carcinoma in situ of cervix
    • carcinoma in situ of uterine cervix
    • carcinoma of cervix stage 0
    • cervical intraepithelial neoplasia grade III with severe dysplasia
    • squamous intraepithelial neoplasia, grade III
Mus musculus (house mouse)
DOID:0070073
  • autosomal dominant intellectual developmental disorder 43
  • Aliases:
    • MRD43
    • autosomal dominant mental retardation 43
    • autosomal dominant non-syndromic intellectual disability 43
Rattus norvegicus (Norway rat)
DOID:1798
  • pancreatic endocrine carcinoma
  • Aliases:
    • Islet cell carcinoma
    • carcinoma of endocrine pancreas
    • malignant neoplasm of islets of Langerhans
    • pancreatic neuroendocrine carcinoma
Mus musculus (house mouse)
DOID:13139
  • crescentic glomerulonephritis
Caenorhabditis elegans
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Last updated: December 9, 2024