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 11601 - 11625 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲ Source
DOID:4676
  • uremia
  • Aliases:
    • UREMIA OF renal ORIGIN
Mus musculus (house mouse)
DOID:8677
  • perinatal necrotizing enterocolitis
  • Aliases:
    • ENTEROCOLITIS NECROTIZING
    • Necrotizing enterocolitis in fetus OR newborn
    • Perinatal necrotising enterocolitis
    • Pseudomembranous enterocolitis in newborn
    • necrotizing enterocolitis
Mus musculus (house mouse)
DOID:2352
  • hemochromatosis
  • Aliases:
    • Haemochromatosis
    • diabetes bronze
    • iron storage disorder
Mus musculus (house mouse)
DOID:0050978
  • spinocerebellar ataxia type 29
Mus musculus (house mouse)
DOID:0070539
  • Halperin-Birk syndrome
  • Aliases:
    • HLBKS
    • NEDSOSB
    • NEURODEVELOPMENTAL DISORDER WITH SPASTIC QUADRIPLEGIA, OPTIC ATROPHY, SEIZURES, AND STRUCTURAL BRAIN ANOMALIES
Mus musculus (house mouse)
DOID:0110290
  • autosomal recessive limb-girdle muscular dystrophy type 2X
  • Aliases:
    • LGMD2X
    • muscular dystrophy, limb-girdle, type 2X
Mus musculus (house mouse)
DOID:3114
  • serous cystadenocarcinoma
  • Aliases:
    • serous adenocarcinoma
    • serous carcinoma
Mus musculus (house mouse)
DOID:0111533
  • gnathodiaphyseal dysplasia
  • Aliases:
    • GDD
    • Levin syndrome 2
    • gnathodiaphyseal sclerosis
    • osteogenesis imperfecta with unusual skeletal lesions
    • osteogenesis imperfecta, Levin type
Mus musculus (house mouse)
DOID:12960
  • acrocephalosyndactylia
  • Aliases:
    • Apert syndrome
Mus musculus (house mouse)
DOID:0090117
  • thiamine-responsive megaloblastic anemia syndrome
  • Aliases:
    • Rogers syndrome
    • THMD1
    • TRMA
    • thiamine metabolism dysfunction syndrome 1
    • thiamine-responsive anaemia syndrome
    • thiamine-responsive anemia syndrome
    • thiamine-responsive megaloblastic anaemia syndrome
    • thiamine-responsive megaloblastic anaemia with diabetes mellitus and sensorineural deafness
    • thiamine-responsive megaloblastic anemia with diabetes mellitus and sensorineural deafness
    • thiamine-responsive myelodysplasia
Mus musculus (house mouse)
DOID:10155
  • intestinal cancer
  • Aliases:
    • malignant intestinal tumors
    • malignant neoplasm of intestine
Mus musculus (house mouse)
DOID:1495
  • cystic echinococcosis
  • Aliases:
    • Echinococcus granulosus infection
    • Echinococcus granulosus infection of lung
    • Echinococcus granulosus infection of thyroid
    • Liver echinococcus granulosus
    • Thyroid echinococcus granulosus
    • echinococcus granulosus
    • echinococcus granulosus infectious disease
    • echinococcus granulosus infectious disease of liver
    • echinococcus granulosus infectious disease of thyroid
    • lung echinococcus granulosus
    • unilocular echinococcosis
    • unilocular hydatid disease
Mus musculus (house mouse)
DOID:3840
  • craniopharyngioma
  • Aliases:
    • neoplasm of Rathke's Pouch
Mus musculus (house mouse)
DOID:8534
  • gastroesophageal reflux disease
  • Aliases:
    • Acid reflux
    • GERD
    • GERD - Gastro-esophageal reflux disease
    • Gastresophageal reflux
    • Gastro-esophageal reflux
    • Gastroesophageal reflux
Mus musculus (house mouse)
DOID:0060772
  • multiple types of congenital heart defects 6
  • Aliases:
    • DTGA3
    • dextro-looped transposition of the great arteries 3
Mus musculus (house mouse)
DOID:14213
  • hypophosphatasia
  • Aliases:
    • deficiency of alkaline phosphatase
Mus musculus (house mouse)
DOID:9402
  • epididymitis
Mus musculus (house mouse)
DOID:0080230
  • autosomal dominant intellectual developmental disorder 54
  • Aliases:
    • autosomal dominant mental retardation 54
Mus musculus (house mouse)
DOID:0110636
  • congenital merosin-deficient muscular dystrophy 1A
  • Aliases:
    • CMD1A
    • MDC1A
    • Merosin-negative congenital muscular dystrophy
    • congenital muscular dystrophy due to laminin alpha2 deficiency
Mus musculus (house mouse)
DOID:583
  • hemolytic anemia
  • Aliases:
    • ANEMIA HEMOLYTIC
Mus musculus (house mouse)
DOID:0090005
  • Schwartz-Jampel syndrome 1
  • Aliases:
    • Aberfeld syndrome
    • Burton skeletal dysplasia
    • Burton syndrome
    • Catel-Hempel syndrome
    • Catel-Hempel type dysostosis enchondralis metaepiphysaria
    • Schwartz-Jampel syndrome type 1
    • Schwartz-Jampel-Aberfeld syndrome
    • myotonic chondrodystrophy
    • myotonic myopathy, dwarfism, chondrodystrophy, ocular and facial anomalies
    • osteochondromuscular dystrophy
Mus musculus (house mouse)
DOID:0110587
  • autosomal dominant nonsyndromic deafness 66
  • Aliases:
    • DFNA66
    • autosomal dominant deafness 66
Mus musculus (house mouse)
DOID:10871
  • age related macular degeneration
  • Aliases:
    • Age Related Maculopathies
    • Age Related Maculopathy
    • Senile macular degeneration
    • Senile macular retinal degeneration
    • age-related macular degeneration
Mus musculus (house mouse)
DOID:4667
  • kyphosis
  • Aliases:
    • Kyphosis deformity of spine
Mus musculus (house mouse)
DOID:0110142
  • Bartter disease type 1
  • Aliases:
    • BARTS1
    • Bartter syndrome type 1
    • Bartter syndrome type 1 antenatal
    • hyperprostaglandin E syndrome 1
    • hypokalemic alkalosis with hypercalciuria 1 antenatal
Mus musculus (house mouse)

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Last updated: December 9, 2024