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 14201 - 14225 of 15957 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism Source
DOID:3744
  • cervical squamous cell carcinoma
  • Aliases:
    • squamous cell carcinoma of cervix
    • squamous cell carcinoma of the Cervix Uteri
Mus musculus (house mouse)
DOID:0111648
  • ectopia lentis with ectopia of pupil
  • Aliases:
    • ectopia lentis et pupillae
Rattus norvegicus (Norway rat)
DOID:0111149
  • autosomal recessive isolated ectopia lentis 2
  • Aliases:
    • ECTOL2
Rattus norvegicus (Norway rat)
DOID:110
  • lens disease
Rattus norvegicus (Norway rat)
DOID:110
  • lens disease
Mus musculus (house mouse)
DOID:0111648
  • ectopia lentis with ectopia of pupil
  • Aliases:
    • ectopia lentis et pupillae
Mus musculus (house mouse)
DOID:0111149
  • autosomal recessive isolated ectopia lentis 2
  • Aliases:
    • ECTOL2
Mus musculus (house mouse)
DOID:0111725
  • geleophysic dysplasia 1
  • Aliases:
    • GPHYSD1
Mus musculus (house mouse)
DOID:1875
  • impotence
  • Aliases:
    • Sexual impotence
    • erectile dysfunction
Mus musculus (house mouse)
DOID:12800
  • mucopolysaccharidosis VI
  • Aliases:
    • MPS VI - Maroteaux-Lamy syndrome
    • Maroteaux - Lamy syndrome
    • Maroteaux-Lamy syndrome
    • arylsulfatase B deficiency
    • deficiency of N-acetylgalactosamine-4-sulfatase
Rattus norvegicus (Norway rat)
DOID:12800
  • mucopolysaccharidosis VI
  • Aliases:
    • MPS VI - Maroteaux-Lamy syndrome
    • Maroteaux - Lamy syndrome
    • Maroteaux-Lamy syndrome
    • arylsulfatase B deficiency
    • deficiency of N-acetylgalactosamine-4-sulfatase
Mus musculus (house mouse)
DOID:0060249
  • scoliosis
Mus musculus (house mouse)
DOID:0080733
  • Ehlers-Danlos syndrome dermatosparaxis type
Mus musculus (house mouse)
DOID:13359
  • Ehlers-Danlos syndrome
  • Aliases:
    • Cutis hyperelastica
    • elastic skin
Mus musculus (house mouse)
DOID:62
  • aortic valve disease
Mus musculus (house mouse)
DOID:1682
  • congenital heart disease
  • Aliases:
    • Congenital Heart Defects
    • Congenital anomaly of heart
    • Heart Malformation
    • congenital heart defect
    • heart defect
Mus musculus (house mouse)
DOID:11383
  • cryptorchidism
  • Aliases:
    • Cryptorchism
    • Undescended testicle
    • Undescended testis
    • undescended testicles
Mus musculus (house mouse)
DOID:0050646
  • distal arthrogryposis
  • Aliases:
    • Arthrogryposis Multiplex Congenita
Mus musculus (house mouse)
DOID:0080177
  • hepatic veno-occlusive disease
  • Aliases:
    • veno-occlusive disease
Mus musculus (house mouse)
DOID:11247
  • disseminated intravascular coagulation
  • Aliases:
    • DIC
    • Defibrination syndrome
    • Diffuse or disseminated intravascular coagulation
Mus musculus (house mouse)
DOID:13133
  • HELLP syndrome
Mus musculus (house mouse)
DOID:10772
  • thrombotic thrombocytopenic purpura
  • Aliases:
    • Moschcowitz's syndrome
Mus musculus (house mouse)
DOID:0080301
  • atypical hemolytic-uremic syndrome
Mus musculus (house mouse)
DOID:9074
  • systemic lupus erythematosus
  • Aliases:
    • Lupus Erythematosus, systemic
    • SLE - Lupus Erythematosus, systemic
    • disseminated lupus erythematosus
Mus musculus (house mouse)
DOID:0050475
  • Weill-Marchesani syndrome
  • Aliases:
    • GEMSS syndrome
    • Marchesani-Weill Syndrome
    • Mesodermal Dysmorphodystrophy, Congenital
    • Spherophakia Brachymorphia Syndrome
    • congenital mesodermal dystrophy
Mus musculus (house mouse)

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Acknowledgements

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