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 776 - 800 of 4621 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲
DOID:1142
  • alternating exotropia
Homo sapiens (human)
DOID:0110229
  • cataract 6 multiple types
  • Aliases:
    • CTRCT6
Homo sapiens (human)
DOID:9268
  • glycine encephalopathy
  • Aliases:
    • Non-ketotic hyperglycinemia
    • nonketotic hyperglycinemia
Homo sapiens (human)
DOID:0110205
  • Charcot-Marie-Tooth disease dominant intermediate E
  • Aliases:
    • CMTDIE
    • Charcot-Marie-Tooth disease-nephropathy syndrome
    • Charcot-Marie-Tooth neuropathy with focal segmental glomerulonephritis
    • autosomal dominant intermediate Charcot-Marie-Tooth disease type E
Homo sapiens (human)
DOID:0060395
  • chromosome 15q24 deletion syndrome
  • Aliases:
    • 15q24 microdeletion syndrome
Homo sapiens (human)
DOID:1793
  • pancreatic cancer
  • Aliases:
    • Ca body of pancreas
    • Ca head of pancreas
    • Ca tail of pancreas
    • malignant neoplasm of body of pancreas
    • malignant neoplasm of head of pancreas
    • malignant neoplasm of tail of pancreas
    • pancreas neoplasm
    • pancreatic neoplasm
    • pancreatic tumor
Homo sapiens (human)
DOID:9719
  • neovascular inflammatory vitreoretinopathy
  • Aliases:
    • ADNIV
    • Retinitis proliferans
    • autosomal dominant neovascular inflammatory vitreoretinopathy
    • proliferative vitreoretinopathy
Homo sapiens (human)
DOID:2012
  • Nezelof syndrome
  • Aliases:
    • Nezelof's syndrome
    • T-cell immunodeficiency with thymic aplasia
    • TIDTA
    • thymic aplasia
    • thymic dysplasia with normal immunoglobulins
Homo sapiens (human)
DOID:13374
  • fibrodysplasia ossificans progressiva
  • Aliases:
    • Stone Man Syndrome
    • myositis ossificans progressiva
    • progressive myositis ossificans
    • progressive ossifying myositis
Homo sapiens (human)
DOID:5566
  • mature teratoma
Homo sapiens (human)
DOID:2755
  • Mycobacterium avium complex disease
  • Aliases:
    • Infection due to Mycobacterium intracellulare
    • MAC disease
    • Mycobacterium Avium Infection
    • Mycobacterium avium Complex
Homo sapiens (human)
DOID:10241
  • thalassemia
  • Aliases:
    • Sickle-cell thalassemia with crisis
    • Sickle-cell thalassemia without crisis
    • thalassemia Hb-S disease with crisis
    • thalassemia Hb-S disease without crisis
Homo sapiens (human)
DOID:0050486
  • exanthem
Homo sapiens (human)
DOID:0040085
  • bacterial sepsis
Homo sapiens (human)
DOID:9253
  • gastrointestinal stromal tumor
  • Aliases:
    • GANT
    • GIST
    • Stromal tumor of gastrointestinal tract
    • Stromal tumour of gastrointestinal tract
    • gastrointestinal stromal tumour
Homo sapiens (human)
DOID:10690
  • mastitis
  • Aliases:
    • Inflammatory breast disease
    • Inflammatory disease of breast
    • breast inflammation
Homo sapiens (human)
DOID:10175
  • optic papillitis
  • Aliases:
    • papillitis
Homo sapiens (human)
DOID:468
  • intramuscular hemangioma
  • Aliases:
    • Intramuscular Angioma
Homo sapiens (human)
DOID:10325
  • silicosis
  • Aliases:
    • Pneumoconiosis due to silicates
    • Silica pneumoconiosis
    • Silicotic fibrosis of lung
    • silicotuberculosis
Homo sapiens (human)
DOID:0060415
  • chromosome 2p16.1-p15 deletion syndrome
  • Aliases:
    • 2p15p16.1 microdeletion syndrome
Homo sapiens (human)
DOID:0050885
  • IMAGe syndrome
  • Aliases:
    • intrauterine growth restriction, metaphyseal dysplasia, adrenal hypoplasia congenita, genital abnormalities
Homo sapiens (human)
DOID:0110509
  • autosomal recessive nonsyndromic deafness 53
  • Aliases:
    • DFNB53
    • autosomal recessive deafness 53
Homo sapiens (human)
DOID:0050567
  • orofacial cleft
Homo sapiens (human)
DOID:0110159
  • Charcot-Marie-Tooth disease type 2B
  • Aliases:
    • CMT2B
    • Charcot-Marie-Tooth neuropathy type 2B
    • HMSN IIB
    • HMSN2B
    • autosomal dominant Charcot-Marie-Tooth disease type 2B
    • hereditary motor and sensory nueropathy IIB
Homo sapiens (human)
DOID:13272
  • Klebsiella pneumonia
  • Aliases:
    • Pneumonia due to Klebsiella pneumoniae
    • Pneumonia due to Klebsiella pneumoniae (disorder)
Homo sapiens (human)

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Last updated: August 19, 2024