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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 9901 - 9925 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Organism Source
DOID:12995
  • conduct disorder
Homo sapiens (human)
DOID:0060040
  • pervasive developmental disorder
  • Aliases:
    • Pervasive Child Development Disorders
    • pervasive development disorder
Homo sapiens (human)
DOID:7596
  • asbestos-related lung carcinoma
Caenorhabditis elegans
DOID:0111020
  • cone-rod dystrophy 9
  • Aliases:
    • CORD9
Caenorhabditis elegans
DOID:0060075
  • estrogen-receptor positive breast cancer
Caenorhabditis elegans
DOID:9498
  • pulmonary eosinophilia
Caenorhabditis elegans
DOID:0070113
  • Niemann-Pick disease type C1
  • Aliases:
    • NPC1
Mus musculus (house mouse)
DOID:14504
  • Niemann-Pick disease
  • Aliases:
    • Sphingomyelinase Deficiency Disease
    • lipoid histiocytosis
    • sphingomyelin lipidosis
Mus musculus (house mouse)
DOID:0110725
  • neuronal ceroid lipofuscinosis 10
  • Aliases:
    • CLN10
    • Cathepsin D deficiency
    • neuronal ceroid lipofuscinosis cathepsin D-deficient
    • neuronal ceroid lipofuscinosis due to cathepsin D deficiency
Caenorhabditis elegans
DOID:14503
  • neuronal ceroid lipofuscinosis
  • Aliases:
    • hereditary ceroid lipofuscinosis
Caenorhabditis elegans
DOID:0111428
  • essential tremor 1
  • Aliases:
    • ETM1
    • hereditary essential tremor 1
Homo sapiens (human)
DOID:0050425
  • restless legs syndrome
  • Aliases:
    • WED
    • Willis-Ekbom disease
    • Wittmaack-Ekbom syndrome
Homo sapiens (human)
DOID:4990
  • essential tremor
  • Aliases:
    • benign essential tremor
    • essential hereditary tremor
    • shaky hand syndrome
Homo sapiens (human)
DOID:0090060
  • Wolcott-Rallison syndrome
Caenorhabditis elegans
DOID:0111019
  • cone-rod dystrophy 12
  • Aliases:
    • CORD12
Caenorhabditis elegans
DOID:0070517
  • retinal macular dystrophy 2
  • Aliases:
    • MCDR2
Caenorhabditis elegans
DOID:0110376
  • retinitis pigmentosa 41
  • Aliases:
    • RP41
Caenorhabditis elegans
DOID:0111343
  • lateral meningocele syndrome
  • Aliases:
    • Lehman syndrome
Mus musculus (house mouse)
DOID:0111035
  • CADASIL 1
  • Aliases:
    • autosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy type 1
Mus musculus (house mouse)
DOID:0080109
  • infantile myofibromatosis
  • Aliases:
    • lipofibromatosis
Mus musculus (house mouse)
DOID:251
  • alcohol-induced mental disorder
Homo sapiens (human)
DOID:12700
  • hyperprolactinemia
  • Aliases:
    • Chiari-Frommel syndrome
    • Pregnancy-related A-G syndrome
    • hyperprolactinaemia
Homo sapiens (human)
DOID:1742
  • drug psychosis
  • Aliases:
    • Drug-induced psychosis
    • Drug-induced psychotic disorder
Homo sapiens (human)
DOID:3602
  • toxic encephalopathy
  • Aliases:
    • neurotoxicity
    • neurotoxicity syndrome
Homo sapiens (human)
DOID:480
  • movement disease
Homo sapiens (human)
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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