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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 3451 - 3475 of 4649 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source ▼
DOID:0080413
  • developmental and epileptic encephalopathy 18
  • Aliases:
    • DEE18
    • early infantile epileptic encephalopathy 18
Homo sapiens (human)
DOID:0080411
  • familial adenomatous polyposis 3
Homo sapiens (human)
DOID:0080410
  • familial adenomatous polyposis 2
  • Aliases:
    • MUTYH-associated polyposis
    • MUTYH-related attenuated FAP
    • MUTYH-related attenuated familial adenomatous polyposis
    • MUTYH-related attenuated familial polyposis coli
Homo sapiens (human)
DOID:0080409
  • familial adenomatous polyposis 1
Homo sapiens (human)
DOID:0080404
  • orofacial cleft 11
  • Aliases:
    • nonsyndromic cleft lip with or without cleft palate 11
Homo sapiens (human)
DOID:0080403
  • orofacial cleft 10
  • Aliases:
    • nonsyndromic cleft lip with or without cleft palate 10
Homo sapiens (human)
DOID:0080394
  • nephrotic syndrome type 19
Homo sapiens (human)
DOID:0080393
  • nephrotic syndrome type 18
Homo sapiens (human)
DOID:0080390
  • nephrotic syndrome type 1
  • Aliases:
    • Finnish congenital nephrosis
Homo sapiens (human)
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:0080387
  • nephrotic syndrome type 12
Homo sapiens (human)
DOID:0080386
  • nephrotic syndrome type 10
Homo sapiens (human)
DOID:0080385
  • nephrotic syndrome type 11
Homo sapiens (human)
DOID:0080384
  • nephrotic syndrome type 6
Homo sapiens (human)
DOID:0080382
  • nephrotic syndrome type 3
  • Aliases:
    • early onset nephrotic syndrome type 3
Homo sapiens (human)
DOID:0080381
  • nephrotic syndrome type 13
Homo sapiens (human)
DOID:0080380
  • nephrotic syndrome type 5
  • Aliases:
    • nephrotic syndrome type 5, with or without ocular abnormalities
Homo sapiens (human)
DOID:0080379
  • nephrotic syndrome type 2
  • Aliases:
    • steroid-resistant autosomal recessive nephrotic syndrome
Homo sapiens (human)
DOID:0080377
  • peroxisomal biogenesis disorder
Homo sapiens (human)
DOID:0080376
  • trichorhinophalangeal syndrome type III
  • Aliases:
    • trichorhinophalangeal syndrome type 3
Homo sapiens (human)
DOID:0080365
  • endometrial hyperplasia
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:0080353
  • X-linked recessive hypophosphatemic rickets
Homo sapiens (human)
DOID:0080352
  • X-linked chondrodysplasia punctata 2
  • Aliases:
    • Conradi-Hunermann Syndrome
    • Happle 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: December 9, 2024