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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 10176 - 10200 of 15957 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism Source
DOID:0060887
  • ossification of the posterior longitudinal ligament of spine
  • Aliases:
    • OPLL
Rattus norvegicus (Norway rat)
DOID:1214
  • tympanosclerosis
Rattus norvegicus (Norway rat)
DOID:0080333
  • aortic valve disease 1
Rattus norvegicus (Norway rat)
DOID:1214
  • tympanosclerosis
Mus musculus (house mouse)
DOID:0080333
  • aortic valve disease 1
Mus musculus (house mouse)
DOID:1800
  • neuroendocrine carcinoma
Rattus norvegicus (Norway rat)
DOID:12783
  • migraine without aura
  • Aliases:
    • common migraine
Rattus norvegicus (Norway rat)
DOID:1800
  • neuroendocrine carcinoma
Mus musculus (house mouse)
DOID:12783
  • migraine without aura
  • Aliases:
    • common migraine
Mus musculus (house mouse)
DOID:1800
  • neuroendocrine carcinoma
Drosophila melanogaster (fruit fly)
DOID:12783
  • migraine without aura
  • Aliases:
    • common migraine
Drosophila melanogaster (fruit fly)
DOID:1712
  • aortic valve stenosis
  • Aliases:
    • Aortic stenosis
    • Rheumatic aortic stenosis
    • rheumatic aortic valve stenosis
Drosophila melanogaster (fruit fly)
DOID:1037
  • lymphoid leukemia
  • Aliases:
    • lymphoblastic leukaemia
    • lymphoblastic leukemia
    • lymphocytic leukaemia
Mus musculus (house mouse)
DOID:0110056
  • amelogenesis imperfecta type 1C
  • Aliases:
    • AI1C
    • amelogenesis imperfecta type IC
    • autosomal recessive amelogenesis imperfecta hypoplastic with or without openbite malocclusion
    • autosomal recessive amelogenesis imperfecta local hypoplastic type
Mus musculus (house mouse)
DOID:0110052
  • amelogenesis imperfecta type 1B
  • Aliases:
    • AI1B
    • AIH2
    • amelogenesis imperfecta type IB
    • autosomal dominant hypoplastic local amelogenesis imperfecta
    • hereditary localized enamel hypoplasia
Mus musculus (house mouse)
DOID:0080386
  • nephrotic syndrome type 10
Mus musculus (house mouse)
DOID:0111169
  • subcortical band heterotopia
  • Aliases:
    • HeCo
    • band heterotopia
    • double cortex syndrome
    • heterotopic cortex
    • subcortical laminar heterotopia
Mus musculus (house mouse)
DOID:2490
  • congenital nervous system abnormality
  • Aliases:
    • congenital neurologic anomaly
Mus musculus (house mouse)
DOID:0081399
  • autosomal dominant distal hereditary motor neuronopathy 10
Mus musculus (house mouse)
DOID:0070246
  • X-linked Emery-Dreifuss muscular dystrophy 1
  • Aliases:
    • EDMD1
    • EMD1
    • Emery-Dreifuss muscular dystrophy 1, X-linked
    • humeroperoneal neuromuscular disease
    • muscular dystrophy, tardive, Dreifuss-Emery type, with contractures
    • scapuloperoneal syndrome, X-linked
Mus musculus (house mouse)
DOID:11726
  • Emery-Dreifuss muscular dystrophy
  • Aliases:
    • EDMD
Mus musculus (house mouse)
DOID:0081276
  • cerebellar atrophy, visual impairment, and psychomotor retardation
  • Aliases:
    • CAVIPMR
Rattus norvegicus (Norway rat)
DOID:10155
  • intestinal cancer
  • Aliases:
    • malignant intestinal tumors
    • malignant neoplasm of intestine
Rattus norvegicus (Norway rat)
DOID:0081276
  • cerebellar atrophy, visual impairment, and psychomotor retardation
  • Aliases:
    • CAVIPMR
Mus musculus (house mouse)
DOID:11589
  • Riley-Day syndrome
  • Aliases:
    • HSAN III
    • familial autonomic nervous dysfunction
    • familial dysautonomia
Mus musculus (house mouse)
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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