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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 1226 - 1250 of 4649 in total
Disease ID ▲ Disease Name Gene Symbol Gene ID Organism Source
DOID:0080384
  • nephrotic syndrome type 6
Homo sapiens (human)
DOID:0080385
  • nephrotic syndrome type 11
Homo sapiens (human)
DOID:0080386
  • nephrotic syndrome type 10
Homo sapiens (human)
DOID:0080387
  • nephrotic syndrome type 12
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:0080390
  • nephrotic syndrome type 1
  • Aliases:
    • Finnish congenital nephrosis
Homo sapiens (human)
DOID:0080393
  • nephrotic syndrome type 18
Homo sapiens (human)
DOID:0080394
  • nephrotic syndrome type 19
Homo sapiens (human)
DOID:0080403
  • orofacial cleft 10
  • Aliases:
    • nonsyndromic cleft lip with or without cleft palate 10
Homo sapiens (human)
DOID:0080404
  • orofacial cleft 11
  • Aliases:
    • nonsyndromic cleft lip with or without cleft palate 11
Homo sapiens (human)
DOID:0080409
  • familial adenomatous polyposis 1
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:0080411
  • familial adenomatous polyposis 3
Homo sapiens (human)
DOID:0080413
  • developmental and epileptic encephalopathy 18
  • Aliases:
    • DEE18
    • early infantile epileptic encephalopathy 18
Homo sapiens (human)
DOID:0080414
  • developmental and epileptic encephalopathy 15
  • Aliases:
    • DEE15
    • early infantile epileptic encephalopathy 15
Homo sapiens (human)
DOID:0080415
  • developmental and epileptic encephalopathy 23
  • Aliases:
    • DEE23
    • Early-onset epileptic encephalopathy-cortical blindness-intellectual disability-facial dysmorphism syndrome
    • Epilepsy-cortical blindness-intellectual disability-facial dysmorphism syndrome
    • early infantile epileptic encephalopathy 23
Homo sapiens (human)
DOID:0080416
  • developmental and epileptic encephalopathy 32
  • Aliases:
    • DEE32
    • early infantile epileptic encephalopathy 32
Homo sapiens (human)
DOID:0080418
  • developmental and epileptic encephalopathy 54
  • Aliases:
    • DEE54
    • early infantile epileptic encephalopathy 54
Homo sapiens (human)
DOID:0080419
  • developmental and epileptic encephalopathy 50
  • Aliases:
    • CDG syndrome type Iz
    • CDG-Iz
    • Carbohydrate deficient glycoprotein syndrome type Iz
    • Congenital disorder of glycosylation type 1z
    • DEE50
    • early infantile epileptic encephalopathy 50
Homo sapiens (human)
DOID:0080420
  • developmental and epileptic encephalopathy 62
  • Aliases:
    • DEE62
    • early infantile epileptic encephalopathy 62
Homo sapiens (human)
DOID:0080421
  • developmental and epileptic encephalopathy 11
  • Aliases:
    • DEE11
    • early infantile epileptic encephalopathy 11
Homo sapiens (human)
DOID:0080422
  • Dravet syndrome
  • Aliases:
    • DEE6
    • DEE6A
    • developmental and epileptic encephalopathy 6
    • developmental and epileptic encephalopathy 6A
    • early infantile epileptic encephalopathy 6
    • severe myoclonic epilepsy of infancy
Homo sapiens (human)
DOID:0080425
  • developmental and epileptic encephalopathy 47
  • Aliases:
    • DEE47
    • early infantile epileptic encephalopathy 47
Homo sapiens (human)
DOID:0080428
  • developmental and epileptic encephalopathy 45
  • Aliases:
    • DEE45
    • early infantile epileptic encephalopathy 45
Homo sapiens (human)
DOID:0080429
  • developmental and epileptic encephalopathy 24
  • Aliases:
    • DEE24
    • early infantile epileptic encephalopathy 24
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