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 2476 - 2500 of 4621 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲
DOID:0060537
  • mitochondrial complex II deficiency
  • Aliases:
    • isolated mitochondrial respiratory chain complex II deficiency
    • isolated succinate-CoQ reductase deficiency
    • isolated succinate-coenzyme Q reductase deficiency
    • isolated succinate-ubiquinone reductase deficiency
Homo sapiens (human)
DOID:0110462
  • autosomal recessive nonsyndromic deafness 101
  • Aliases:
    • DFNB101
    • autosomal recessive deafness 101
Homo sapiens (human)
DOID:0110561
  • autosomal dominant nonsyndromic deafness 31
  • Aliases:
    • DFNA31
    • autosomal dominant deafness 31
Homo sapiens (human)
DOID:0060123
  • connective tissue benign neoplasm
  • Aliases:
    • mesenchymal tissue neoplasm
    • neoplasm of soft tissue
    • neoplasm of soft tissues
    • soft tissue benign neoplasm
    • tumor of the soft tissue
Homo sapiens (human)
DOID:0110246
  • cataract 26 multiple types
  • Aliases:
    • CTRCT26
Homo sapiens (human)
DOID:5303
  • cervical clear cell adenocarcinoma
  • Aliases:
    • Clear cell carcinoma of the Cervix Uteri
Homo sapiens (human)
DOID:2859
  • hemoglobin C disease
  • Aliases:
    • Hb-C disease
Homo sapiens (human)
DOID:0110114
  • atrial heart septal defect 9
  • Aliases:
    • ASD9
    • atrial septal defect 9
Homo sapiens (human)
DOID:1324
  • lung cancer
Homo sapiens (human)
DOID:0060245
  • Mast syndrome
  • Aliases:
    • SPG21
    • autosomal recessive spastic paraplegia 21
    • autosomal recessive spastic paraplegia type 21
    • hereditary spastic paraplegia 21
Homo sapiens (human)
DOID:0110810
  • hereditary spastic paraplegia 5A
  • Aliases:
    • SPG5A
    • autosomal recessive spastic paraplegia 5A
    • autosomal recessive spastic paraplegia type 5A
Homo sapiens (human)
DOID:0110038
  • Alzheimer's disease 6
  • Aliases:
    • AD6
    • Alzheimer disease 6
    • Alzheimer disease 6, late onset
Homo sapiens (human)
DOID:5522
  • basaloid squamous cell carcinoma
  • Aliases:
    • Basaloid carcinoma
Homo sapiens (human)
DOID:0060891
  • Parkinson's disease 19A
  • Aliases:
    • juvenile onset Parkinson disease 19A
    • juvenile onset Parkinson's disease 19A
Homo sapiens (human)
DOID:8719
  • in situ carcinoma
Homo sapiens (human)
DOID:0070004
  • myeloid neoplasm
Homo sapiens (human)
DOID:0060170
  • generalized epilepsy with febrile seizures plus
  • Aliases:
    • GEFS+
Homo sapiens (human)
DOID:0080547
  • metabolic dysfunction-associated steatohepatitis
  • Aliases:
    • MASH
    • NASH
    • non-alcoholic steatohepatitis
    • nonalcoholic steatohepatitis
Homo sapiens (human)
DOID:3523
  • brain stem infarction
  • Aliases:
    • Brainstem infarction
Homo sapiens (human)
DOID:11573
  • listeriosis
  • Aliases:
    • Infection by Listeria monocytogenes
    • Listeria infection
Homo sapiens (human)
DOID:0050431
  • arrhythmogenic right ventricular cardiomyopathy
  • Aliases:
    • ARVC
    • ARVC cardiomyopathy
    • ARVD
    • arrhythmogenic right ventricular dysplasia
    • arrhythmogenic right ventricular dysplasia/cardiomyopathy
    • right ventricular ACM
Homo sapiens (human)
DOID:1788
  • peritoneal mesothelioma
  • Aliases:
    • Advanced malignant Mesothelioma of Peritoneum
    • advanced malignant peritoneal mesothelioma
    • malignant mesothelioma of peritoneum
Homo sapiens (human)
DOID:0060400
  • chromosome 16p12.2-p11.2 deletion syndrome
  • Aliases:
    • 16p11.2-p12.2 microdeletion syndrome
    • 16p11.2p12.2 microdeletion syndrome
Homo sapiens (human)
DOID:8850
  • salivary gland cancer
  • Aliases:
    • malignant neoplasm of salivary gland
Homo sapiens (human)
DOID:0060643
  • primary sclerosing cholangitis
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