GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB), DisGeNET, and Alliance of Genome Resources is integrated into one list.

Source Last Updated
Alliance of Genome Resources July 29, 2024
DisGeNET July 29, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 4151 - 4175 of 4621 in total
Disease ID Disease Name ▼ Gene Symbol Gene ID Organism
DOID:0060586
  • Noonan syndrome 8
  • Aliases:
    • NS8
Homo sapiens (human)
DOID:0060585
  • Noonan syndrome 7
  • Aliases:
    • NS7
Homo sapiens (human)
DOID:0060584
  • Noonan syndrome 6
  • Aliases:
    • NS6
Homo sapiens (human)
DOID:0060583
  • Noonan syndrome 5
  • Aliases:
    • NS5
Homo sapiens (human)
DOID:0060582
  • Noonan syndrome 4
  • Aliases:
    • NS4
Homo sapiens (human)
DOID:0060581
  • Noonan syndrome 3
  • Aliases:
    • NS3
Homo sapiens (human)
DOID:0060580
  • Noonan syndrome 2
  • Aliases:
    • NS2
Homo sapiens (human)
DOID:0060588
  • Noonan syndrome 10
  • Aliases:
    • NS10
Homo sapiens (human)
DOID:0060578
  • Noonan syndrome 1
  • Aliases:
    • NS1
Homo sapiens (human)
DOID:7400
  • Nijmegen breakage syndrome
  • Aliases:
    • Berlin breakage syndrome
    • Microcephaly, normal intelligence and immunodeficiency
    • NBS
    • Seemanova syndrome II
    • Seemanova syndrome type 2
    • ataxia-telangiectasia variant
    • immunodeficiency-microcephaly-chromosomal instability syndrome
    • microcephaly-immunodeficiency-lymphoreticuloma syndrome
Homo sapiens (human)
DOID:14504
  • Niemann-Pick disease
  • Aliases:
    • Sphingomyelinase Deficiency Disease
    • lipoid histiocytosis
    • sphingomyelin lipidosis
Homo sapiens (human)
DOID:0070114
  • Niemann-Pick disease type C2
  • Aliases:
    • NPC2
Homo sapiens (human)
DOID:0070113
  • Niemann-Pick disease type C1
  • Aliases:
    • NPC1
Homo sapiens (human)
DOID:0070112
  • Niemann-Pick disease type B
Homo sapiens (human)
DOID:0070111
  • Niemann-Pick disease type A
Homo sapiens (human)
DOID:2012
  • Nezelof syndrome
  • Aliases:
    • Nezelof's syndrome
    • T-cell immunodeficiency with thymic aplasia
    • TIDTA
    • thymic aplasia
    • thymic dysplasia with normal immunoglobulins
Homo sapiens (human)
DOID:0050474
  • Netherton syndrome
Homo sapiens (human)
DOID:0060346
  • Native American myopathy
  • Aliases:
    • Bailey-Bloch congenital myopathy
    • congenital myopathy 13
Homo sapiens (human)
DOID:0060599
  • Nance-Horan syndrome
Homo sapiens (human)
DOID:0060463
  • NUT midline carcinoma
  • Aliases:
    • nuclear protein in testis midline carcinoma
Homo sapiens (human)
DOID:0060728
  • NGLY1-deficiency
  • Aliases:
    • NGLY1-CDDG
    • congenital disorder of deglycosylation
    • congenital disorder of glycosylation type Iv
    • deficiency of N-glycanase 1
Homo sapiens (human)
DOID:0060409
  • NFIA-related disorder
  • Aliases:
    • 1p31p32 microdeletion syndrome
    • Chromosome 1, Monosomy 1p32
    • brain malformations with or without urinary tract defects
    • chromosome 1p32-p31 deletion syndrome
Homo sapiens (human)
DOID:13276
  • Mycoplasma pneumoniae pneumonia
  • Aliases:
    • Mycoplasma pneumonia
    • Mycoplasmal pneumonia
    • Pneumonia due to Eaton's agent
    • Pneumonia due to Mycoplasma pneumoniae
    • Pneumonia due to Mycoplasma pneumoniae (disorder)
    • cold agglutinin positive pneumonia
Homo sapiens (human)
DOID:2755
  • Mycobacterium avium complex disease
  • Aliases:
    • Infection due to Mycobacterium intracellulare
    • MAC disease
    • Mycobacterium Avium Infection
    • Mycobacterium avium Complex
Homo sapiens (human)
DOID:0050465
  • Muir-Torre syndrome
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: August 19, 2024