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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 2276 - 2300 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source ▲
DOID:0060850
  • annular pancreas
Danio rerio (zebrafish)
DOID:0060851
  • pemphigus vulgaris
  • Aliases:
    • familial pemphigus vulgaris
Homo sapiens (human)
DOID:0060851
  • pemphigus vulgaris
  • Aliases:
    • familial pemphigus vulgaris
Mus musculus (house mouse)
DOID:0060852
  • Pierson syndrome
  • Aliases:
    • microcoria-congenital nephrosis syndrome
Homo sapiens (human)
DOID:0060852
  • Pierson syndrome
  • Aliases:
    • microcoria-congenital nephrosis syndrome
Rattus norvegicus (Norway rat)
DOID:0060852
  • Pierson syndrome
  • Aliases:
    • microcoria-congenital nephrosis syndrome
Mus musculus (house mouse)
DOID:0060852
  • Pierson syndrome
  • Aliases:
    • microcoria-congenital nephrosis syndrome
Caenorhabditis elegans
DOID:0060852
  • Pierson syndrome
  • Aliases:
    • microcoria-congenital nephrosis syndrome
Drosophila melanogaster (fruit fly)
DOID:0060853
  • Potocki-Lupski syndrome
  • Aliases:
    • 17p11.2 microduplication syndrome
    • chromosome 17p11.2 duplication syndrome
    • trisomy 17p11.2
Homo sapiens (human)
DOID:0060853
  • Potocki-Lupski syndrome
  • Aliases:
    • 17p11.2 microduplication syndrome
    • chromosome 17p11.2 duplication syndrome
    • trisomy 17p11.2
Mus musculus (house mouse)
DOID:0060854
  • autosomal recessive pseudohypoaldosteronism type 1
  • Aliases:
    • PHA1B
    • autosomal recessive PHA 1
Rattus norvegicus (Norway rat)
DOID:0060854
  • autosomal recessive pseudohypoaldosteronism type 1
  • Aliases:
    • PHA1B
    • autosomal recessive PHA 1
Homo sapiens (human)
DOID:0060854
  • autosomal recessive pseudohypoaldosteronism type 1
  • Aliases:
    • PHA1B
    • autosomal recessive PHA 1
Mus musculus (house mouse)
DOID:0060854
  • autosomal recessive pseudohypoaldosteronism type 1
  • Aliases:
    • PHA1B
    • autosomal recessive PHA 1
Caenorhabditis elegans
DOID:0060855
  • autosomal dominant pseudohypoaldosteronism type 1
  • Aliases:
    • PHA1A
    • autosomal dominant PHA 1
Homo sapiens (human)
DOID:0060856
  • right atrial isomerism
  • Aliases:
    • Ivemark syndrome
    • asplenia with cardiovascular anomalies
Mus musculus (house mouse)
DOID:0060856
  • right atrial isomerism
  • Aliases:
    • Ivemark syndrome
    • asplenia with cardiovascular anomalies
Rattus norvegicus (Norway rat)
DOID:0060856
  • right atrial isomerism
  • Aliases:
    • Ivemark syndrome
    • asplenia with cardiovascular anomalies
Caenorhabditis elegans
DOID:0060856
  • right atrial isomerism
  • Aliases:
    • Ivemark syndrome
    • asplenia with cardiovascular anomalies
Homo sapiens (human)
DOID:0060858
  • hypotonia-cystinuria syndrome
  • Aliases:
    • cystinuria with mitochondrial disease
Homo sapiens (human)
DOID:0060859
  • salmonellosis
  • Aliases:
    • Salmonella infection
Mus musculus (house mouse)
DOID:0060859
  • salmonellosis
  • Aliases:
    • Salmonella infection
Homo sapiens (human)
DOID:0060861
  • microphthalmia with limb anomalies
  • Aliases:
    • MLA
    • OAS
    • Waardenburg anophthalmia syndrome
    • anophthalmia-syndactyly syndrome
    • ophthalmoacromelic syndrome
Mus musculus (house mouse)
DOID:0060861
  • microphthalmia with limb anomalies
  • Aliases:
    • MLA
    • OAS
    • Waardenburg anophthalmia syndrome
    • anophthalmia-syndactyly syndrome
    • ophthalmoacromelic syndrome
Homo sapiens (human)
DOID:0060863
  • patterned macular dystrophy
  • Aliases:
    • patterned dystrophy of retinal pigment epithelium
Rattus norvegicus (Norway rat)
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Last updated: December 9, 2024