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 15301 - 15325 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼ Source
DOID:5614
  • eye disease
Caenorhabditis elegans
DOID:0060682
  • autosomal dominant nocturnal frontal lobe epilepsy 1
  • Aliases:
    • ENFL1
    • nocturnal frontal lobe epilepsy 1
Caenorhabditis elegans
DOID:1380
  • endometrial cancer
  • Aliases:
    • endometrial Ca
    • endometrial neoplasm
    • malignant endometrial neoplasm
    • malignant neoplasm of endometrium
    • neoplasm of endometrium
    • primary malignant neoplasm of endometrium
    • tumor of Endometrium
Caenorhabditis elegans
DOID:0111432
  • essential tremor 5
  • Aliases:
    • ETM5
    • hereditary essential tremor 5
Caenorhabditis elegans
DOID:0111535
  • progressive osseous heteroplasia
  • Aliases:
    • POH
    • ectopic ossification familial type
    • familial ectopic ossification
    • osteoma cutis
Caenorhabditis elegans
DOID:0060075
  • estrogen-receptor positive breast cancer
Caenorhabditis elegans
DOID:0081182
  • autosomal recessive intellectual developmental disorder 6
Caenorhabditis elegans
DOID:0060650
  • dicarboxylic aminoaciduria
  • Aliases:
    • glutamate-aspartate transport defect
Caenorhabditis elegans
DOID:0080334
  • aortic valve disease 2
Caenorhabditis elegans
DOID:13223
  • uterine fibroid
  • Aliases:
    • Plexiform leiomyoma
    • UTERUS FIBROMA
    • leiomyoma of Corpus Uteri
    • uterine leiomyoma
Caenorhabditis elegans
DOID:0060691
  • platelet-type bleeding disorder 16
  • Aliases:
    • autosomal dominant Glanzmann thrombasthenia
    • autosomal dominant thrombasthenia of Glanzmann and Naegeli
Caenorhabditis elegans
DOID:1067
  • open-angle glaucoma
  • Aliases:
    • Wide-angle glaucoma
    • glaucoma simplex
    • open angle glaucoma
    • pigmentary glaucoma
Caenorhabditis elegans
DOID:10487
  • Hirschsprung's disease
  • Aliases:
    • Hirschsprung disease
    • aganglionic megacolon
    • congenital megacolon
    • macrocolon
    • pelvirectal achalasia
    • total intestinal aganglionosis
Caenorhabditis elegans
DOID:0112216
  • developmental and epileptic encephalopathy 80
  • Aliases:
    • DEE80
    • GPIBD20
    • early infantile epileptic encephalopathy 80
    • glycosylphosphatidylinositol biosynthesis defect 20
Caenorhabditis elegans
DOID:0070093
  • schizophrenia 18
  • Aliases:
    • Chromosome 7q36.3 Duplication Syndrome, 362-Kb
    • SCZD18
Caenorhabditis elegans
DOID:13359
  • Ehlers-Danlos syndrome
  • Aliases:
    • Cutis hyperelastica
    • elastic skin
Caenorhabditis elegans
DOID:0112121
  • nephrogenic syndrome of inappropriate antidiuresis
  • Aliases:
    • NSIAD
Caenorhabditis elegans
DOID:0080177
  • hepatic veno-occlusive disease
  • Aliases:
    • veno-occlusive disease
Caenorhabditis elegans
DOID:13515
  • tuberous sclerosis
  • Aliases:
    • Bourneville's disease
    • Epiloia
    • Tuberose sclerosis
    • Tuberous sclerosis syndrome
    • cerebral sclerosis
Caenorhabditis elegans
DOID:783
  • end stage renal disease
  • Aliases:
    • end stage renal failure
    • end-stage kidney disease
Caenorhabditis elegans
DOID:2747
  • glycogen storage disease
  • Aliases:
    • glycogenosis
Caenorhabditis elegans
DOID:1307
  • dementia
Caenorhabditis elegans
DOID:11949
  • Creutzfeldt-Jakob disease
  • Aliases:
    • CJD
    • Creutzfeldt Jacob syndrome
    • Creutzfeldt Jakob disease
    • Creutzfeldt-Jacob disease
    • Jakob-Creutzfeldt disease
    • Subacute spongiform encephalopathy
    • Transmissible virus dementia
Caenorhabditis elegans
DOID:0110639
  • congenital muscular dystrophy due to integrin alpha-7 deficiency
  • Aliases:
    • congenital muscular dystrophy with ITGA7 deficiency
    • congenital muscular dystrophy with integrin alpha-7 deficiency
    • congenital myopathy due to integrin alpha-7 deficiency
Caenorhabditis elegans
DOID:0111150
  • autosomal dominant isolated ectopia lentis 1
  • Aliases:
    • ECTOL1
Caenorhabditis elegans

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Last updated: December 9, 2024