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 July 29, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 3376 - 3400 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Organism
DOID:4976
  • elephantiasis
Homo sapiens (human)
DOID:3118
  • hepatobiliary disease
  • Aliases:
    • liver and biliary tract disease
Homo sapiens (human)
DOID:8791
  • breast carcinoma in situ
  • Aliases:
    • Non-Infiltrating carcinoma of breast
    • carcinoma in situ of breast
Homo sapiens (human)
DOID:0050580
  • hereditary lymphedema
Homo sapiens (human)
DOID:0070210
  • hereditary lymphedema IA
  • Aliases:
    • LMPH1A
Homo sapiens (human)
DOID:0070212
  • hereditary lymphedema I
  • Aliases:
    • LMPH1
    • Milroy disease
    • Nonne-Milroy lymphedema
    • PCL
    • congenital primary lymphedema
    • hereditary lymphedema type I
Homo sapiens (human)
DOID:4977
  • lymphedema
  • Aliases:
    • Lymphatic edema
    • Lymphoedema
Homo sapiens (human)
DOID:0060198
  • amyotrophic lateral sclerosis type 6
  • Aliases:
    • ALS6
    • amyotrophic lateral sclerosis 6, with or without frontotemporal dementia
    • autosomal recessive amyotrophic lateral sclerosis 6
Homo sapiens (human)
DOID:0070433
  • hyperphosphatasia with impaired intellectual development syndrome 1
  • Aliases:
    • GPIBD2
    • HPMRS1
    • glycosylphosphatidylinositol biosynthesis defect 2
    • hyperphosphatasia with mental retardation syndrome 1
Mus musculus (house mouse)
DOID:916
  • liver benign neoplasm
  • Aliases:
    • epithelial hepatic and intrahepatic bile duct neoplasm
Mus musculus (house mouse)
DOID:9869
  • hereditary fructose intolerance syndrome
  • Aliases:
    • Fructosaemia
    • Fructose-1,6-bisphosphate aldolase B deficiency
    • Fructosemia
Mus musculus (house mouse)
DOID:0110798
  • hereditary spastic paraplegia 46
  • Aliases:
    • SPG46
    • autosomal recessive spastic paraplegia 46
    • autosomal recessive spastic paraplegia type 46
Mus musculus (house mouse)
DOID:438
  • autoimmune disease of the nervous system
Homo sapiens (human)
DOID:11573
  • listeriosis
  • Aliases:
    • Infection by Listeria monocytogenes
    • Listeria infection
Homo sapiens (human)
DOID:4617
  • periapical granuloma
  • Aliases:
    • Apical granuloma
Homo sapiens (human)
DOID:823
  • periapical periodontitis
  • Aliases:
    • Apical periodontitis
Homo sapiens (human)
DOID:11269
  • chronic apical periodontitis
Homo sapiens (human)
DOID:0060704
  • lymphoproliferative syndrome
  • Aliases:
    • Combined immunodeficiency due to ITK deficiency
Homo sapiens (human)
DOID:0080319
  • X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia
  • Aliases:
    • XMEN
Homo sapiens (human)
DOID:0110910
  • leukocyte adhesion deficiency 1
  • Aliases:
    • LAD1
    • LFA1 immunodeficiency
    • leukocyte adhesion deficiency type I
    • lymphocyte function-associated antigen 1 immunodeficiency
Homo sapiens (human)
DOID:4231
  • histiocytoma
Homo sapiens (human)
DOID:495
  • sclerosing hemangioma
  • Aliases:
    • Sclerosing haemangioma
Homo sapiens (human)
DOID:4419
  • benign deep fibrous histiocytoma
Homo sapiens (human)
DOID:4394
  • reticulohistiocytic granuloma
  • Aliases:
    • Reticulohistiocytoma
    • solitary reticulohistiocytoma
Homo sapiens (human)
DOID:11168
  • anogenital venereal wart
  • Aliases:
    • Anogenital Human papilloma Virus Infectious Disease
    • Anogenital warts
    • Genital warts
    • genital wart virus infectious disease
    • venereal wart
Homo sapiens (human)

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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