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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 15601 - 15625 of 15957 in total
Disease ID Disease Name ▼ Gene Symbol Gene ID Organism Source
DOID:0050834
  • CHARGE syndrome
  • Aliases:
    • CHARGE association
Mus musculus (house mouse)
DOID:0060337
  • CEDNIK syndrome
  • Aliases:
    • cerebral dysgenesis, neuropathy, ichthyosis and keratoderma syndrome
Homo sapiens (human)
DOID:0060337
  • CEDNIK syndrome
  • Aliases:
    • cerebral dysgenesis, neuropathy, ichthyosis and keratoderma syndrome
Mus musculus (house mouse)
DOID:0060022
  • CD40 ligand deficiency
  • Aliases:
    • HIGMX-1
    • X-linked hyper-IgM syndrome
Mus musculus (house mouse)
DOID:0060022
  • CD40 ligand deficiency
  • Aliases:
    • HIGMX-1
    • X-linked hyper-IgM syndrome
Homo sapiens (human)
DOID:0060022
  • CD40 ligand deficiency
  • Aliases:
    • HIGMX-1
    • X-linked hyper-IgM syndrome
Rattus norvegicus (Norway rat)
DOID:0080207
  • CAKUT2
  • Aliases:
    • Congenital anomalies of the kidney and urinary tract 2
Xenopus laevis (African clawed frog)
DOID:0080207
  • CAKUT2
  • Aliases:
    • Congenital anomalies of the kidney and urinary tract 2
Rattus norvegicus (Norway rat)
DOID:0080207
  • CAKUT2
  • Aliases:
    • Congenital anomalies of the kidney and urinary tract 2
Caenorhabditis elegans
DOID:0080207
  • CAKUT2
  • Aliases:
    • Congenital anomalies of the kidney and urinary tract 2
Homo sapiens (human)
DOID:0080207
  • CAKUT2
  • Aliases:
    • Congenital anomalies of the kidney and urinary tract 2
Drosophila melanogaster (fruit fly)
DOID:0080207
  • CAKUT2
  • Aliases:
    • Congenital anomalies of the kidney and urinary tract 2
Mus musculus (house mouse)
DOID:0080206
  • CAKUT1
  • Aliases:
    • Congenital anomalies of the kidney and urinary tract 1
Homo sapiens (human)
DOID:0080205
  • CAKUT
  • Aliases:
    • Congenital anomalies of the kidney and urinary tract
    • Renal or urinary tract malformation
Homo sapiens (human)
DOID:0080205
  • CAKUT
  • Aliases:
    • Congenital anomalies of the kidney and urinary tract
    • Renal or urinary tract malformation
Drosophila melanogaster (fruit fly)
DOID:0080205
  • CAKUT
  • Aliases:
    • Congenital anomalies of the kidney and urinary tract
    • Renal or urinary tract malformation
Rattus norvegicus (Norway rat)
DOID:0080205
  • CAKUT
  • Aliases:
    • Congenital anomalies of the kidney and urinary tract
    • Renal or urinary tract malformation
Mus musculus (house mouse)
DOID:0080205
  • CAKUT
  • Aliases:
    • Congenital anomalies of the kidney and urinary tract
    • Renal or urinary tract malformation
Xenopus laevis (African clawed frog)
DOID:0080205
  • CAKUT
  • Aliases:
    • Congenital anomalies of the kidney and urinary tract
    • Renal or urinary tract malformation
Caenorhabditis elegans
DOID:0111035
  • CADASIL 1
  • Aliases:
    • autosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy type 1
Drosophila melanogaster (fruit fly)
DOID:0111035
  • CADASIL 1
  • Aliases:
    • autosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy type 1
Caenorhabditis elegans
DOID:0111035
  • CADASIL 1
  • Aliases:
    • autosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy type 1
Homo sapiens (human)
DOID:0111035
  • CADASIL 1
  • Aliases:
    • autosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy type 1
Mus musculus (house mouse)
DOID:0111035
  • CADASIL 1
  • Aliases:
    • autosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy type 1
Rattus norvegicus (Norway rat)
DOID:0111581
  • C syndrome
  • Aliases:
    • OTCS
    • Opitz C trigonocephaly
    • Opitz trigonocephaly C syndrome
    • Opitz trigonocephaly syndrome
    • trigonocephaly C syndrome
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: August 19, 2024