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 451 - 475 of 4621 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Organism
DOID:0112303
  • spondylometaphyseal dysplasia with corneal dystrophy
  • Aliases:
    • SMDCD
Homo sapiens (human)
DOID:14566
  • disease of cellular proliferation
  • Aliases:
    • cell process disease
    • neoplasm
Homo sapiens (human)
DOID:0111677
  • familial benign fleck retina
  • Aliases:
    • FRFB
Homo sapiens (human)
DOID:0111246
  • amyotrophic lateral sclerosis-parkinsonism/dementia complex 1
  • Aliases:
    • ALS-PDC
    • Amyotrophic lateral sclerosis-parkinsonism-dementia of Guam syndrome
    • Guam disease
    • Lytico-Bodig disease
    • PDALS
    • amyotrophic lateral sclerosis-parkinsonism/dementia complex of Guam
    • parkinsonism-dementia-ALS complex
Homo sapiens (human)
DOID:9439
  • chronic cholangitis
Homo sapiens (human)
DOID:4012
  • papillary transitional carcinoma
  • Aliases:
    • Papillary transitional cell carcinoma
Homo sapiens (human)
DOID:0060652
  • familial erythrocytosis 1
  • Aliases:
    • ECYT1
    • autosomal dominant benign erythrocytosis
    • primary familial and congenital polycythemia
Homo sapiens (human)
DOID:0060340
  • ciliopathy
Homo sapiens (human)
DOID:0050876
  • Caroli disease
Homo sapiens (human)
DOID:6255
  • growth hormone secreting pituitary adenoma
  • Aliases:
    • Growth Hormone Producing adenoma of the Pituitary
    • Somatotroph adenoma
    • growth hormone secreting adenoma of pituitary
Homo sapiens (human)
DOID:0060484
  • EAST syndrome
  • Aliases:
    • SeSAME syndrome
    • epilepsy, ataxia, sensorineural deafness and tubulopathy
    • seizures, sensorineural deafness, ataxia, mental retardation and electrolyte imbalance
Homo sapiens (human)
DOID:0060337
  • CEDNIK syndrome
  • Aliases:
    • cerebral dysgenesis, neuropathy, ichthyosis and keratoderma syndrome
Homo sapiens (human)
DOID:0112347
  • hereditary spastic paraplegia 84
  • Aliases:
    • SPG84
    • spastic paraplegia 84 autosomal recessive
Homo sapiens (human)
DOID:0060413
  • chromosome 22q11.2 deletion syndrome, distal
  • Aliases:
    • DiGeorge syndrome and Velocardiofacial syndrome
    • distal 22q11.2 microdeletion syndrome
Homo sapiens (human)
DOID:0050211
  • swine influenza
Homo sapiens (human)
DOID:0111936
  • immunodeficiency 14
  • Aliases:
    • APDS
    • IMD14
    • PASLI disease
    • activated PI3K-delta syndrome
    • senescent T-cells-lymphadenopathy-immunodeficiency syndrome due to p110delta-activating mutation
Homo sapiens (human)
DOID:10301
  • parotitis
Homo sapiens (human)
DOID:10303
  • sialadenitis
  • Aliases:
    • Sialoadenitis
Homo sapiens (human)
DOID:5895
  • clear cell cystadenofibroma
Homo sapiens (human)
DOID:14731
  • Weaver syndrome
  • Aliases:
    • WEAVER-LIKE SYNDROME
    • Weaver-Williams syndrome
Homo sapiens (human)
DOID:5479
  • papillary adenofibroma
Homo sapiens (human)
DOID:12003
  • trachea squamous cell carcinoma
  • Aliases:
    • Tracheal Epidermoid carcinoma
Homo sapiens (human)
DOID:0060075
  • estrogen-receptor positive breast cancer
Homo sapiens (human)
DOID:2683
  • adenofibroma
Homo sapiens (human)
DOID:2636
  • ovarian Brenner tumor
  • Aliases:
    • benign ovarian Brenner tumor
    • benign ovarian Brenner tumour
    • ovarian Brenner tumour
Homo sapiens (human)

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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