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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 11601 - 11625 of 15957 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Organism Source
DOID:409
  • liver disease
  • Aliases:
    • disorder of liver
    • hepatic disorder
Drosophila melanogaster (fruit fly)
DOID:0060186
  • chemical colitis
Drosophila melanogaster (fruit fly)
DOID:0110536
  • autosomal recessive nonsyndromic deafness 91
  • Aliases:
    • DFNB91
    • autosomal recessive deafness 91
Drosophila melanogaster (fruit fly)
DOID:2452
  • thrombophilia
  • Aliases:
    • hypercoagulability state
Drosophila melanogaster (fruit fly)
DOID:640
  • encephalomyelitis
  • Aliases:
    • Encephalitis &/or myelitis
Rattus norvegicus (Norway rat)
DOID:0070484
  • Legius syndrome
  • Aliases:
    • LGSS
    • NF1-like syndrome
    • neurofibromatosis type 1-like syndrome
Mus musculus (house mouse)
DOID:0110916
  • hereditary spherocytosis type 1
  • Aliases:
    • HS1
    • SPH1
    • hereditary spherocytosis 1
Mus musculus (house mouse)
DOID:0110918
  • hereditary spherocytosis type 3
  • Aliases:
    • HS3
    • SPH3
    • hereditary spherocytosis 3
Mus musculus (house mouse)
DOID:0050882
  • spinocerebellar ataxia type 5
Mus musculus (house mouse)
DOID:0070162
  • hereditary sensory and autonomic neuropathy type 1
  • Aliases:
    • HSAN1
    • hereditary sensory and autonomic neuropathy type I
Mus musculus (house mouse)
DOID:0070157
  • hereditary sensory and autonomic neuropathy type 1C
  • Aliases:
    • HSAN1C
    • hereditary sensory and autonomic neuropathy type IC
Mus musculus (house mouse)
DOID:5408
  • Paget's disease of bone
  • Aliases:
    • Paget disease of bone
    • Paget's bone disease
    • osseous Paget's disease
    • osteitis deformans
Mus musculus (house mouse)
DOID:0081366
  • Paget's disease of bone 3
  • Aliases:
    • Paget disease of bone-3
Mus musculus (house mouse)
DOID:0110068
  • frontotemporal dementia and/or amyotrophic lateral sclerosis 3
  • Aliases:
    • FTDALS3
Mus musculus (house mouse)
DOID:0081364
  • neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset
Mus musculus (house mouse)
DOID:0081363
  • distal myopathy with rimmed vacuoles
Mus musculus (house mouse)
DOID:0060249
  • scoliosis
Rattus norvegicus (Norway rat)
DOID:0060720
  • autosomal recessive congenital ichthyosis 11
  • Aliases:
    • IFAH syndrome
    • IHS
    • autosomal recessive ichthyosis with hypotrichosis
    • hypotrichosis-congenital ichthyosis syndrome
    • ichthyosis and follicular atrophoderma with hypotrichosis and hypohidrosis
    • ichthyosis-follicular atrophoderma-hypotrichosis syndrome
    • ichthyosis-follicular atrophoderma-hypotrichosis-hypohidrosis syndrome
    • ichthyosis-hypotrichosis syndrome
Mus musculus (house mouse)
DOID:0080414
  • developmental and epileptic encephalopathy 15
  • Aliases:
    • DEE15
    • early infantile epileptic encephalopathy 15
Mus musculus (house mouse)
DOID:0081180
  • autosomal recessive intellectual developmental disorder 12
Mus musculus (house mouse)
DOID:0081180
  • autosomal recessive intellectual developmental disorder 12
Rattus norvegicus (Norway rat)
DOID:0080414
  • developmental and epileptic encephalopathy 15
  • Aliases:
    • DEE15
    • early infantile epileptic encephalopathy 15
Rattus norvegicus (Norway rat)
DOID:0060470
  • salt and pepper syndrome
  • Aliases:
    • salt & pepper syndrome
    • salt-and-pepper syndrome
Mus musculus (house mouse)
DOID:0060470
  • salt and pepper syndrome
  • Aliases:
    • salt & pepper syndrome
    • salt-and-pepper syndrome
Rattus norvegicus (Norway rat)
DOID:3261
  • hyper IgE recurrent infection syndrome 1
  • Aliases:
    • Job syndrome
    • Job's syndrome
    • hyperimmunoglobulin E syndrome
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