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 4676 - 4700 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲
DOID:14699
  • thrombocytopenia-absent radius syndrome
  • Aliases:
    • Radial aplasia-thrombocytopenia syndrome
    • Thrombocytopenia with absent radii (TAR) syndrome
Homo sapiens (human)
DOID:2365
  • West Nile encephalitis
  • Aliases:
    • West Nile Fever with encephalitis
    • West Nile fever encephalitis
Homo sapiens (human)
DOID:0110761
  • type 1 diabetes mellitus 24
  • Aliases:
    • IDDM24
    • Insulin-Dependent Diabetes Mellitus 24
Homo sapiens (human)
DOID:0110668
  • congenital myasthenic syndrome 10
  • Aliases:
    • CMS10
    • LGM
    • congenital muscular dystrophy merosin-positive
    • familial limb-girdle myasthenia
Homo sapiens (human)
DOID:0110206
  • Charcot-Marie-Tooth disease dominant intermediate F
  • Aliases:
    • CMTDIF
    • autosomal dominant intermediate Charcot-Marie-Tooth disease type F
Homo sapiens (human)
DOID:0111420
  • familial GPIHBP1 deficiency
  • Aliases:
    • familial glycosylphosphatidylinositol-anchored high density lipoprotein-binding protein 1 deficiency
    • hyperlipoproteinemia type 1D
    • hyperlipoproteinemia type ID
Homo sapiens (human)
DOID:4176
  • blood group incompatibility
Homo sapiens (human)
DOID:10793
  • chronic sphenoidal sinusitis
  • Aliases:
    • Sphenoidal sinus-chr.
Homo sapiens (human)
DOID:0080071
  • mucolipidosis III alpha/beta
  • Aliases:
    • mucolipidosis III
    • pseudo-Hurler polydystrophy
Homo sapiens (human)
DOID:0050466
  • Loeys-Dietz syndrome
Homo sapiens (human)
DOID:14555
  • Foster-Kennedy syndrome
Homo sapiens (human)
DOID:2368
  • gangliosidosis
Homo sapiens (human)
DOID:0111353
  • arthrogryposis, renal dysfunction, and cholestasis 1
  • Aliases:
    • ARCS1
Homo sapiens (human)
DOID:0110152
  • Charcot-Marie-Tooth disease type 1B
  • Aliases:
    • CMT1B
    • Charcot-Marie-Tooth disease slow nerve conduction type linked to Duffy
    • Charcot-Marie-Tooth neuropathy type 1B
    • HMSN IB
    • HMSN1B
    • autosomal dominant Charcot-Marie-Tooth disease with focally folded myelin sheaths type 1B
    • hereditary motor and sensory neuropathy IB
    • peroneal muscular atrophy
Homo sapiens (human)
DOID:11840
  • coronary artery vasospasm
  • Aliases:
    • Coronary Vasospasm
    • Coronary artery spasm
Homo sapiens (human)
DOID:1492
  • obsolete eye and adnexa disease
Homo sapiens (human)
DOID:5505
  • papillary ependymoma
Homo sapiens (human)
DOID:9861
  • miliary tuberculosis
  • Aliases:
    • Disseminated tuberculosis
    • Tuberculosis miliaris disseminata
    • acute miliary tuberculosis
    • generalized tuberculosis
Homo sapiens (human)
DOID:0110261
  • cataract 35
  • Aliases:
    • CATCN1
    • CTRCT35
    • autosomal recessive congenital nuclear cataract 1
    • cataract 35, congenital nuclear
Homo sapiens (human)
DOID:0060455
  • Thiel-Behnke corneal dystrophy
  • Aliases:
    • TBCD
    • Waardenburg-Jonker corneal dystrophy
    • anterior limiting membrane dystrophy type II
    • corneal dystrophy honeycomb-shaped
    • corneal dystrophy of Bowman layer type II
Homo sapiens (human)
DOID:4511
  • breast angiosarcoma
  • Aliases:
    • hemangiosarcoma of the breast
Homo sapiens (human)
DOID:12003
  • trachea squamous cell carcinoma
  • Aliases:
    • Tracheal Epidermoid carcinoma
Homo sapiens (human)
DOID:0110477
  • autosomal recessive nonsyndromic deafness 2
  • Aliases:
    • DFNB2
    • autosomal recessive deafness 2
Homo sapiens (human)
DOID:0080664
  • diaphyseal medullary stenosis with malignant fibrous histiocytoma
  • Aliases:
    • Hardcastle syndrome
    • bone dysplasia-medullary fibrosarcoma syndrome
    • diaphyseal medullary stenosis-malignant fibrous histiocytoma syndrome
Homo sapiens (human)
DOID:841
  • extrinsic allergic alveolitis
  • Aliases:
    • alveolitis
    • hypersensitivity pneumonitis
Homo sapiens (human)

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Last updated: August 19, 2024