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 14601 - 14625 of 15957 in total
Disease ID Disease Name ▲ Gene Symbol Gene ID Organism Source
DOID:3114
  • serous cystadenocarcinoma
  • Aliases:
    • serous adenocarcinoma
    • serous carcinoma
Rattus norvegicus (Norway rat)
DOID:3114
  • serous cystadenocarcinoma
  • Aliases:
    • serous adenocarcinoma
    • serous carcinoma
Mus musculus (house mouse)
DOID:2945
  • severe acute respiratory syndrome
  • Aliases:
    • SARS
    • SARS-CoV infection
Rattus norvegicus (Norway rat)
DOID:2945
  • severe acute respiratory syndrome
  • Aliases:
    • SARS
    • SARS-CoV infection
Danio rerio (zebrafish)
DOID:2945
  • severe acute respiratory syndrome
  • Aliases:
    • SARS
    • SARS-CoV infection
Mus musculus (house mouse)
DOID:2945
  • severe acute respiratory syndrome
  • Aliases:
    • SARS
    • SARS-CoV infection
Xenopus laevis (African clawed frog)
DOID:2945
  • severe acute respiratory syndrome
  • Aliases:
    • SARS
    • SARS-CoV infection
Drosophila melanogaster (fruit fly)
DOID:2945
  • severe acute respiratory syndrome
  • Aliases:
    • SARS
    • SARS-CoV infection
Homo sapiens (human)
DOID:2945
  • severe acute respiratory syndrome
  • Aliases:
    • SARS
    • SARS-CoV infection
Caenorhabditis elegans
DOID:2945
  • severe acute respiratory syndrome
  • Aliases:
    • SARS
    • SARS-CoV infection
Xenopus tropicalis (tropical clawed frog)
DOID:0090012
  • severe combined immunodeficiency with sensitivity to ionizing radiation
  • Aliases:
    • SCID due to DCLRE1C deficiency
    • SCID due to artemis deficiency
    • SCID, Athabascan type
    • SCID, Athabaskan type
    • Severe combined immunodeficiency due to DCLRE1C deficiency
    • Severe combined immunodeficiency due to artemis deficiency
    • Severe combined immunodeficiency, Athabascan type
    • Severe combined immunodeficiency, Athabaskan type
    • artemis deficiency
Homo sapiens (human)
DOID:627
  • severe combined immunodeficiency
  • Aliases:
    • SCID
    • combined T and B cell inborn immunodeficiency
Mus musculus (house mouse)
DOID:627
  • severe combined immunodeficiency
  • Aliases:
    • SCID
    • combined T and B cell inborn immunodeficiency
Caenorhabditis elegans
DOID:627
  • severe combined immunodeficiency
  • Aliases:
    • SCID
    • combined T and B cell inborn immunodeficiency
Homo sapiens (human)
DOID:627
  • severe combined immunodeficiency
  • Aliases:
    • SCID
    • combined T and B cell inborn immunodeficiency
Drosophila melanogaster (fruit fly)
DOID:627
  • severe combined immunodeficiency
  • Aliases:
    • SCID
    • combined T and B cell inborn immunodeficiency
Rattus norvegicus (Norway rat)
DOID:0090013
  • severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, Nk cell-positive
  • Aliases:
    • SCID due to complete RAG1-2 deficiency
    • Severe combined immunodeficiency due to complete RAG1-2 deficiency
    • autosomal recessive T cell-negative, B-cell negative, NK cell-positive SCID
Homo sapiens (human)
DOID:0090014
  • severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, Nk cell-positive
  • Aliases:
    • autosomal recessive T cell-negative, B-cell positive, NK cell-positive SCID
Mus musculus (house mouse)
DOID:0090014
  • severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, Nk cell-positive
  • Aliases:
    • autosomal recessive T cell-negative, B-cell positive, NK cell-positive SCID
Homo sapiens (human)
DOID:0111932
  • severe congenital encephalopathy due to MECP2 mutation
  • Aliases:
    • neonatal severe encephalopathy due to MECP2 mutations
    • severe neonatal-onset encephalopathy with microcephaly
Rattus norvegicus (Norway rat)
DOID:0111932
  • severe congenital encephalopathy due to MECP2 mutation
  • Aliases:
    • neonatal severe encephalopathy due to MECP2 mutations
    • severe neonatal-onset encephalopathy with microcephaly
Mus musculus (house mouse)
DOID:0111932
  • severe congenital encephalopathy due to MECP2 mutation
  • Aliases:
    • neonatal severe encephalopathy due to MECP2 mutations
    • severe neonatal-onset encephalopathy with microcephaly
Homo sapiens (human)
DOID:0080625
  • severe congenital neutropenia 1
Mus musculus (house mouse)
DOID:0080625
  • severe congenital neutropenia 1
Homo sapiens (human)
DOID:0112133
  • severe congenital neutropenia 3
  • Aliases:
    • Kostmann disease
    • Kostmann syndrome
    • SCN3
    • infantile agranulocytosis
Homo sapiens (human)

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Last updated: December 9, 2024