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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 7351 - 7375 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source ▼
DOID:0112341
  • hereditary spastic paraplegia 80
  • Aliases:
    • SPG80
    • spastic paraplegia 80 autosomal dominant
Homo sapiens (human)
DOID:0112338
  • spermatogenic failure 57
  • Aliases:
    • SPGF57
Homo sapiens (human)
DOID:0112337
  • spermatogenic failure 55
  • Aliases:
    • SPGF55
Mus musculus (house mouse)
DOID:0112337
  • spermatogenic failure 55
  • Aliases:
    • SPGF55
Homo sapiens (human)
DOID:0112336
  • spermatogenic failure 56
  • Aliases:
    • SPGF56
Homo sapiens (human)
DOID:0112334
  • pontocerebellar hypoplasia type 1C
  • Aliases:
    • PCH1C
Homo sapiens (human)
DOID:0112333
  • pontocerebellar hypoplasia type 16
  • Aliases:
    • PCH16
Mus musculus (house mouse)
DOID:0112333
  • pontocerebellar hypoplasia type 16
  • Aliases:
    • PCH16
Rattus norvegicus (Norway rat)
DOID:0112333
  • pontocerebellar hypoplasia type 16
  • Aliases:
    • PCH16
Saccharomyces cerevisiae S288C
DOID:0112333
  • pontocerebellar hypoplasia type 16
  • Aliases:
    • PCH16
Drosophila melanogaster (fruit fly)
DOID:0112333
  • pontocerebellar hypoplasia type 16
  • Aliases:
    • PCH16
Homo sapiens (human)
DOID:0112332
  • pontocerebellar hypoplasia type 13
  • Aliases:
    • PCH13
Homo sapiens (human)
DOID:0112332
  • pontocerebellar hypoplasia type 13
  • Aliases:
    • PCH13
Mus musculus (house mouse)
DOID:0112329
  • pontocerebellar hypoplasia type 2F
  • Aliases:
    • PCH2F
Homo sapiens (human)
DOID:0112321
  • alacrima, achalasia, and impaired intellectual development syndrome
  • Aliases:
    • AAMR
    • alacrima, achalasia, and mental retardation syndrome
Homo sapiens (human)
DOID:0112319
  • Kanzaki disease
  • Aliases:
    • NAGA deficiency type 2
    • adult-onset alpha-N-acetylgalactosaminidase deficiency
    • alpha-N-acetylgalactosaminidase deficiency type 2
Rattus norvegicus (Norway rat)
DOID:0112319
  • Kanzaki disease
  • Aliases:
    • NAGA deficiency type 2
    • adult-onset alpha-N-acetylgalactosaminidase deficiency
    • alpha-N-acetylgalactosaminidase deficiency type 2
Caenorhabditis elegans
DOID:0112319
  • Kanzaki disease
  • Aliases:
    • NAGA deficiency type 2
    • adult-onset alpha-N-acetylgalactosaminidase deficiency
    • alpha-N-acetylgalactosaminidase deficiency type 2
Mus musculus (house mouse)
DOID:0112318
  • Schindler disease type 1
  • Aliases:
    • NAGA deficiency type 1
    • alpha-N-acetylgalactosaminidase deficiency type 1
Caenorhabditis elegans
DOID:0112318
  • Schindler disease type 1
  • Aliases:
    • NAGA deficiency type 1
    • alpha-N-acetylgalactosaminidase deficiency type 1
Rattus norvegicus (Norway rat)
DOID:0112318
  • Schindler disease type 1
  • Aliases:
    • NAGA deficiency type 1
    • alpha-N-acetylgalactosaminidase deficiency type 1
Mus musculus (house mouse)
DOID:0112315
  • brain small vessel disease 3
  • Aliases:
    • BSVD3
Caenorhabditis elegans
DOID:0112315
  • brain small vessel disease 3
  • Aliases:
    • BSVD3
Mus musculus (house mouse)
DOID:0112315
  • brain small vessel disease 3
  • Aliases:
    • BSVD3
Homo sapiens (human)
DOID:0112315
  • brain small vessel disease 3
  • Aliases:
    • BSVD3
Xenopus laevis (African clawed frog)
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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