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 October 9, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 5426 - 5450 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼ Source
DOID:4449
  • macular retinal edema
  • Aliases:
    • macular edema
    • macular oedema
    • macular retinal oedema
Mus musculus (house mouse)
DOID:3587
  • pancreatic ductal carcinoma
  • Aliases:
    • malignant neoplasm of duct of Wirsung
    • pancreatic duct cancer
Mus musculus (house mouse)
DOID:0111480
  • combined oxidative phosphorylation deficiency 10
  • Aliases:
    • COXPD10
    • infantile hypertrophic mitochondrial cardiomyopathy and lactic acidosis
    • mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency
Mus musculus (house mouse)
DOID:3507
  • dermatofibrosarcoma protuberans
Mus musculus (house mouse)
DOID:0110337
  • osteogenesis imperfecta type 7
  • Aliases:
    • OI7
    • osteogenesis imperfecta type VII
Mus musculus (house mouse)
DOID:0070303
  • multiple epiphyseal dysplasia 1
  • Aliases:
    • EDM1
    • MED1
    • multiple epiphyseal dysplasia COMP-related
    • polyepiphyseal dysplasia type 1
Mus musculus (house mouse)
DOID:0110893
  • inflammatory bowel disease 13
  • Aliases:
    • IBD13
Mus musculus (house mouse)
DOID:0080139
  • multiple congenital anomalies-hypotonia-seizures syndrome 2
  • Aliases:
    • developmental and epileptic encephalopathy 20
    • early infantile epileptic encephalopathy 20
    • glycosylphosphatidylinositol biosynthesis defect 4
Mus musculus (house mouse)
DOID:8029
  • sporadic breast cancer
Mus musculus (house mouse)
DOID:0060158
  • acquired metabolic disease
Mus musculus (house mouse)
DOID:0110131
  • Bardet-Biedl syndrome 9
  • Aliases:
    • BBS9
Mus musculus (house mouse)
DOID:0060682
  • autosomal dominant nocturnal frontal lobe epilepsy 1
  • Aliases:
    • ENFL1
    • nocturnal frontal lobe epilepsy 1
Mus musculus (house mouse)
DOID:0070279
  • primary autosomal recessive microcephaly 14
  • Aliases:
    • MCPH14
Mus musculus (house mouse)
DOID:1920
  • hyperuricemia
  • Aliases:
    • Blood urate raized
    • uricacidemia
Mus musculus (house mouse)
DOID:5339
  • cyclic hematopoiesis
  • Aliases:
    • Cyclic neutropenia
    • Cyclical neutropenia
    • Neutropenia, periodic
    • cyclic agranulocytosis
Mus musculus (house mouse)
DOID:1496
  • echinococcosis
  • Aliases:
    • Echinococcosis of liver
    • echinococcal disease
    • hepatic echinococcosis
    • hydatid disease
    • hydatidosis
    • liver echinococcus
    • pulmonary echinococcosis
Mus musculus (house mouse)
DOID:12689
  • acoustic neuroma
  • Aliases:
    • Vestibular Neurilemmoma
    • Vestibular schwannoma
Mus musculus (house mouse)
DOID:1927
  • sphingolipidosis
  • Aliases:
    • sphingolipidoses
Mus musculus (house mouse)
DOID:0060256
  • Dowling-Degos disease
  • Aliases:
    • dark dot disease
    • reticular pigment anomaly of flexures
Mus musculus (house mouse)
DOID:12119
  • hemosiderosis
  • Aliases:
    • haemosiderosis
Mus musculus (house mouse)
DOID:0110248
  • cataract 30
  • Aliases:
    • CTRCT30
    • Dusty cataract
    • cataract 30 pulverulent
    • cataract Coppock-like
Mus musculus (house mouse)
DOID:2326
  • gastroenteritis
  • Aliases:
    • cholera morbus
    • infectious colitis, enteritis and gastroenteritis
Mus musculus (house mouse)
DOID:0111332
  • Pitt-Hopkins-like syndrome 2
  • Aliases:
    • PTHSL2
Mus musculus (house mouse)
DOID:0080998
  • acute necrotizing pancreatitis
Mus musculus (house mouse)
DOID:0111348
  • multiple epiphyseal dysplasia with myopia and deafness
  • Aliases:
    • EDMMD
    • multiple epiphyseal dysplasia, Beighton type
    • multiple epiphyseal dysplasia-myopia-deafness syndrome
Mus musculus (house mouse)

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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: December 9, 2024