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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 9176 - 9200 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Organism Source
DOID:2222
  • factor X deficiency
  • Aliases:
    • disease, Stuart-Prower
Rattus norvegicus (Norway rat)
DOID:0110459
  • dilated cardiomyopathy 1FF
  • Aliases:
    • CMD1FF
Rattus norvegicus (Norway rat)
DOID:0111425
  • restrictive cardiomyopathy 1
  • Aliases:
    • RCM1
    • familial restrictive cardiomyopathy 1
Rattus norvegicus (Norway rat)
DOID:0110313
  • hypertrophic cardiomyopathy 7
  • Aliases:
    • CMH7
    • cardiomyopathy, familial hypertrophic 7
Rattus norvegicus (Norway rat)
DOID:0110460
  • dilated cardiomyopathy 2A
  • Aliases:
    • CMD2A
Rattus norvegicus (Norway rat)
DOID:0080176
  • meningococcal meningitis
Rattus norvegicus (Norway rat)
DOID:0080158
  • herpes simplex virus keratitis
  • Aliases:
    • dendritic keratitis
Rattus norvegicus (Norway rat)
DOID:0050073
  • invasive aspergillosis
Rattus norvegicus (Norway rat)
DOID:1214
  • tympanosclerosis
Rattus norvegicus (Norway rat)
DOID:4677
  • keratitis
Rattus norvegicus (Norway rat)
DOID:10690
  • mastitis
  • Aliases:
    • Inflammatory breast disease
    • Inflammatory disease of breast
    • breast inflammation
Rattus norvegicus (Norway rat)
DOID:3883
  • Lynch syndrome
  • Aliases:
    • COCA 1
    • HNPCC - hereditary nonpolyposis colon cancer
    • Hereditary Defective Mismatch Repair syndrome
    • Hereditary non-polyposis colon cancer
    • Hereditary non-polyposis colon cancer syndrome
    • Hereditary non-polyposis colorectal cancer
    • Hereditary non-polyposis colorectal cancer syndrome
    • Hereditary nonpolyposis colon cancer
    • Hereditary nonpolyposis colon cancer syndrome
    • Hereditary nonpolyposis colorectal cancer syndrome
    • hereditary nonpolyposis colorectal cancer
    • hereditary nonpolyposis colorectal neoplasm
Rattus norvegicus (Norway rat)
DOID:4258
  • Weissenbacher-Zweymuller syndrome
  • Aliases:
    • Piere-Robin syndrome
    • Pierre Robin Malformation
Rattus norvegicus (Norway rat)
DOID:0070063
  • autosomal dominant intellectual developmental disorder 33
  • Aliases:
    • MRD33
    • autosomal dominant mental retardation 33
    • autosomal dominant non-syndromic intellectual disability 33
Rattus norvegicus (Norway rat)
DOID:0081112
  • Baraitser-Winter syndrome 1
Rattus norvegicus (Norway rat)
DOID:13832
  • patent ductus arteriosus
  • Aliases:
    • Patent ductus Botalli
Rattus norvegicus (Norway rat)
DOID:0110550
  • autosomal dominant nonsyndromic deafness 20
  • Aliases:
    • DFNA20
    • DFNA26
    • autosomal dominant deafness 20
Rattus norvegicus (Norway rat)
DOID:13099
  • Moyamoya disease
  • Aliases:
    • progressive intracranial arterial occlusion
Rattus norvegicus (Norway rat)
DOID:0110317
  • hypertrophic cardiomyopathy 11
  • Aliases:
    • CMH11
    • cardiomyopathy familial hypertrophic 11
Rattus norvegicus (Norway rat)
DOID:0110456
  • dilated cardiomyopathy 1R
  • Aliases:
    • CMD1R
Rattus norvegicus (Norway rat)
DOID:0110110
  • atrial heart septal defect 5
  • Aliases:
    • ASD5
    • atrial septal defect 5
Rattus norvegicus (Norway rat)
DOID:0060358
  • multiple acyl-CoA dehydrogenase deficiency
  • Aliases:
    • MAD deficiency
    • MADD
    • electron transfer flavoprotein deficiency
    • electron transfer flavoprotein ubiquinone oxidoreductase deficiency
    • glutaric acidemia type 2
    • glutaric aciduria type 2
Rattus norvegicus (Norway rat)
DOID:0050814
  • temtamy preaxial brachydactyly syndrome
  • Aliases:
    • PREAXIAL BRACHYDACTYLY SYNDROME, TEMTAMY TYPE
Rattus norvegicus (Norway rat)
DOID:0080335
  • mitochondrial DNA depletion syndrome 12b
Homo sapiens (human)
DOID:0111517
  • autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2
  • Aliases:
    • PEOA2
    • autosomal dominant progressive external ophthalmoplegia 2
Homo sapiens (human)
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Last updated: December 9, 2024