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 3701 - 3725 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼
DOID:119
  • vaginal cancer
  • Aliases:
    • malignant neoplasm of vagina
    • malignant tumor of vagina
    • malignant vaginal tumor
    • neoplasm of vagina
    • vagina neoplasm
    • vaginal tumor
Homo sapiens (human)
DOID:13664
  • post-vaccinal encephalitis
  • Aliases:
    • Encephalitis following immunization procedures
    • Postvaccinal encephalomyelitis
Homo sapiens (human)
DOID:0060179
  • Renpenning syndrome
  • Aliases:
    • Golabi-Ito-Hall syndrome
    • Sutherland-Haan X-linked mental retardation syndrome
    • X-linked intellectual disability due to PQBP1 mutations
    • X-linked intellectual disability, Renpenning type
    • X-linked mental retardation Renpenning type
    • X-linked mental retardation with spastic diplegia
    • syndromic X-linked mental retardation 8
Homo sapiens (human)
DOID:0060336
  • 3-methylglutaconic aciduria
Homo sapiens (human)
DOID:0111691
  • familial adult myoclonic epilepsy 5
  • Aliases:
    • FAME5
    • FCMTE5
    • familial cortical myoclonic tremor and epilepsy 5
Homo sapiens (human)
DOID:3847
  • papillary craniopharyngioma
  • Aliases:
    • Papillary Rathke's Pouch tumor
    • craniopharyngioma, papillary
Homo sapiens (human)
DOID:4784
  • immune-complex glomerulonephritis
  • Aliases:
    • Immune Complex Glomerulonephritis
Homo sapiens (human)
DOID:0110732
  • neuronal ceroid lipofuscinosis 11
  • Aliases:
    • CLN11
Homo sapiens (human)
DOID:3209
  • junctional epidermolysis bullosa
  • Aliases:
    • congenital junctional epidermolysis bullosa
Homo sapiens (human)
DOID:7378
  • pituitary hypoplasia
Homo sapiens (human)
DOID:0060425
  • chromosome 8q21.11 deletion syndrome
  • Aliases:
    • 8q21.11 microdeletion syndrome
Homo sapiens (human)
DOID:0050387
  • nonpapillary renal cell carcinoma
Homo sapiens (human)
DOID:1639
  • skeletal tuberculosis
  • Aliases:
    • osteoarticular tuberculosis
Homo sapiens (human)
DOID:162
  • cancer
  • Aliases:
    • malignant neoplasm
    • malignant tumor
    • primary cancer
Homo sapiens (human)
DOID:3840
  • craniopharyngioma
  • Aliases:
    • neoplasm of Rathke's Pouch
Homo sapiens (human)
DOID:13580
  • cholestasis
  • Aliases:
    • Obstruction of bile duct
    • bile occlusion
Homo sapiens (human)
DOID:0090046
  • dystonia 21
Homo sapiens (human)
DOID:0110726
  • neuronal ceroid lipofuscinosis 2
  • Aliases:
    • CLN2
    • neuronal ceroid lipofuscinosis 2 variable age at onset
Homo sapiens (human)
DOID:0050467
  • erythrokeratodermia variabilis
  • Aliases:
    • Erythrokeratodermia Figurata Variabilis
    • Greither Disease
Homo sapiens (human)
DOID:12341
  • retroperitoneal sarcoma
Homo sapiens (human)
DOID:11701
  • selective IgA deficiency disease
  • Aliases:
    • Immunoglobulin A deficiency
    • Selective immunoglobulin A deficiency
    • selective IgA immunodeficiency
Homo sapiens (human)
DOID:0060193
  • amyotrophic lateral sclerosis type 1
  • Aliases:
    • ALS1
    • amyotrophic lateral sclerosis 1
Homo sapiens (human)
DOID:8233
  • inflammatory liposarcoma
Homo sapiens (human)
DOID:0060055
  • popliteal pterygium syndrome
  • Aliases:
    • facio-genito-popliteal syndrome
    • popliteal web syndrome
Homo sapiens (human)
DOID:0080005
  • bone remodeling disease
Homo sapiens (human)

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Acknowledgements

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