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 6451 - 6475 of 7942 in total
Disease ID ▼ Disease Name Gene Symbol Gene ID Organism
DOID:0080388
  • nephrotic syndrome type 7
  • Aliases:
    • Ig-mediated MPGN
    • Ig-mediated membranoproliferative glomerulonephritis
    • Immunoglobulin-mediated MPGN
    • immunoglobulin-mediated membranoproliferative glomerulonephritis
    • nephrotic syndrome type 7 with membranoptoliferative glomerulonephritis
Homo sapiens (human)
DOID:0080382
  • nephrotic syndrome type 3
  • Aliases:
    • early onset nephrotic syndrome type 3
Homo sapiens (human)
DOID:0080379
  • nephrotic syndrome type 2
  • Aliases:
    • steroid-resistant autosomal recessive nephrotic syndrome
Homo sapiens (human)
DOID:0080377
  • peroxisomal biogenesis disorder
Saccharomyces cerevisiae S288C
DOID:0080369
  • ovarian sex-cord stromal tumor
Homo sapiens (human)
DOID:0080367
  • chronic eosinophilic leukemia
Homo sapiens (human)
DOID:0080365
  • endometrial hyperplasia
Homo sapiens (human)
DOID:0080362
  • X-linked spondyloepiphyseal dysplasia tarda
Homo sapiens (human)
DOID:0080356
  • IgG4-related disease
Homo sapiens (human)
DOID:0080354
  • Phelan-McDermid syndrome
  • Aliases:
    • 22q13.3 deletion syndrome
    • monosomy 22q13 syndrome
Homo sapiens (human)
DOID:0080352
  • X-linked chondrodysplasia punctata 2
  • Aliases:
    • Conradi-Hunermann Syndrome
    • Happle syndrome
Homo sapiens (human)
DOID:0080351
  • CLOVES syndrome
  • Aliases:
    • congenital lipomatous overgrowth, vascular malformations, and epidermal nevi
Mus musculus (house mouse)
DOID:0080351
  • CLOVES syndrome
  • Aliases:
    • congenital lipomatous overgrowth, vascular malformations, and epidermal nevi
Homo sapiens (human)
DOID:0080351
  • CLOVES syndrome
  • Aliases:
    • congenital lipomatous overgrowth, vascular malformations, and epidermal nevi
Rattus norvegicus (Norway rat)
DOID:0080349
  • developmental and epileptic encephalopathy 39
  • Aliases:
    • AGC1 deficiency
    • early infantile epileptic encephalopathy 39
    • epileptic encephalopathy with global cerebral demyelination
Drosophila melanogaster (fruit fly)
DOID:0080349
  • developmental and epileptic encephalopathy 39
  • Aliases:
    • AGC1 deficiency
    • early infantile epileptic encephalopathy 39
    • epileptic encephalopathy with global cerebral demyelination
Homo sapiens (human)
DOID:0080348
  • Alzheimer's disease 1
  • Aliases:
    • Alzheimer's disease 1, early onset
Homo sapiens (human)
DOID:0080347
  • malignant pheochromocytoma
  • Aliases:
    • Pheochromocytoma, malignant
Homo sapiens (human)
DOID:0080342
  • Simpson-Golabi-Behmel syndrome type 2
Homo sapiens (human)
DOID:0080335
  • mitochondrial DNA depletion syndrome 12b
Homo sapiens (human)
DOID:0080334
  • aortic valve disease 2
Homo sapiens (human)
DOID:0080333
  • aortic valve disease 1
Homo sapiens (human)
DOID:0080333
  • aortic valve disease 1
Drosophila melanogaster (fruit fly)
DOID:0080333
  • aortic valve disease 1
Mus musculus (house mouse)
DOID:0080333
  • aortic valve disease 1
Rattus norvegicus (Norway rat)

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Last updated: August 19, 2024