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 3476 - 3500 of 4621 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Organism
DOID:0060708
  • lymphoproliferative syndrome 2
  • Aliases:
    • CD27 deficiency
    • LPFS2
Homo sapiens (human)
DOID:0060707
  • lymphoproliferative syndrome 1
  • Aliases:
    • LPFS1
Homo sapiens (human)
DOID:0070324
  • systemic Epstein-Barr virus positive T-cell lymphoma of childhood
  • Aliases:
    • EBV-positive T-cell lymphoproliferative disorder of childhood
    • systemic EBV-positive T-cell lymphoma of childhood
Homo sapiens (human)
DOID:0110115
  • autoimmune lymphoproliferative syndrome type 2A
  • Aliases:
    • ALPS2A
    • autoimmune lymphoproliferative syndrome type IIA
Homo sapiens (human)
DOID:0110116
  • autoimmune lymphoproliferative syndrome type 2B
  • Aliases:
    • ALPS with recurrent viral infections
    • ALPS2B
    • CEDS
    • Caspase 8 deficiency
    • Caspase 8 deficiency syndrome
    • Caspase eight deficiency state
    • autoimmune lymphoproliferative syndrome type IIB
    • autoimmune lymphoproliferative syndrome with recurrent viral infections
Homo sapiens (human)
DOID:8864
  • acute monocytic leukemia
  • Aliases:
    • acute Monoblastic Leukemia and acute Monocytic Leukemia
    • acute monocytic leukaemia
    • acute monocytic leukaemia without mention of remission
    • acute monocytic leukemia without mention of remission
    • acute monocytic leukemia, FAB M5
    • acute monocytic leukemia, morphology
Homo sapiens (human)
DOID:0070258
  • congenital disorder of glycosylation type IIf
  • Aliases:
    • CDG IIf
    • CDG2F
    • CDGIIdf
    • CMP-sialic acid transporter deficiency
    • Carbohydrate deficient glycoprotein syndrome type IIf
    • SLC35A1-CDG
Homo sapiens (human)
DOID:3488
  • cellulitis
Homo sapiens (human)
DOID:3389
  • Papillon-Lefevre disease
  • Aliases:
    • Papillon Lefevre syndrome
    • Papillon-Lefvre syndrome
Homo sapiens (human)
DOID:0080568
  • congenital disorder of glycosylation Iq
  • Aliases:
    • congenital disorder of glycosylation 1q
Homo sapiens (human)
DOID:0111005
  • cone-rod dystrophy 2
  • Aliases:
    • CORD2
    • CRD2
    • RCRD2
    • cone-rod retinal dystrophy 2
    • retinal cone-rod dystrophy 2
Homo sapiens (human)
DOID:0090053
  • episodic kinesigenic dyskinesia 1
  • Aliases:
    • Paroxysmal kinesigenic choreoathetosis
Homo sapiens (human)
DOID:9191
  • diabetic macular edema
Homo sapiens (human)
DOID:0050759
  • myotonic dystrophy type 2
Homo sapiens (human)
DOID:681
  • progressive bulbar palsy
Homo sapiens (human)
DOID:576
  • proteinuria
Homo sapiens (human)
DOID:9854
  • lingual-facial-buccal dyskinesia
  • Aliases:
    • Oro-facial dyskinesia
Homo sapiens (human)
DOID:9649
  • congenital nystagmus
Homo sapiens (human)
DOID:11771
  • spontaneous ocular nystagmus
  • Aliases:
    • Ocular nystagmus
    • Searching eye movements
    • visual deprivation nystagmus
Homo sapiens (human)
DOID:9650
  • pathologic nystagmus
Homo sapiens (human)
DOID:13174
  • dissociated nystagmus
Homo sapiens (human)
DOID:0050572
  • cone-rod dystrophy
  • Aliases:
    • cone-rod retinal dystrophy
Homo sapiens (human)
DOID:936
  • brain disease
  • Aliases:
    • encephalopathy
Homo sapiens (human)
DOID:0081381
  • juvenile amyotrophic lateral sclerosis type 27
Homo sapiens (human)
DOID:0070146
  • hereditary sensory neuropathy type 4
  • Aliases:
    • hereditary sensory neuropathy type IV
    • insensitivity to pain, congenital, with anhidrosis
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: August 19, 2024