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 2176 - 2200 of 4621 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼
DOID:14402
  • critical illness polyneuropathy
Homo sapiens (human)
DOID:467
  • venous hemangioma
Homo sapiens (human)
DOID:11836
  • clubfoot
  • Aliases:
    • Congenital equinovarus
    • Equinovarus deformity of foot
    • congenital clubfoot
    • congenital talipes equinovarus
Homo sapiens (human)
DOID:707
  • B-cell lymphoma
  • Aliases:
    • B-cell lymphocytic neoplasm
Homo sapiens (human)
DOID:1587
  • thrombocytopenia due to platelet alloimmunization
  • Aliases:
    • Auto-immune thrombocytopenia
    • Immune thrombocytopenia
    • Thrombocytopenia Due to Immune Destruction
Homo sapiens (human)
DOID:4943
  • adenocarcinoma in situ
Homo sapiens (human)
DOID:0060278
  • pontocerebellar hypoplasia type 9
Homo sapiens (human)
DOID:4085
  • trophoblastic neoplasm
  • Aliases:
    • Trophoblastic tumor
Homo sapiens (human)
DOID:10146
  • thymus lymphoma
Homo sapiens (human)
DOID:8454
  • riboflavin deficiency
  • Aliases:
    • ariboflavinosis
    • vitamin B2 deficiency
Homo sapiens (human)
DOID:4163
  • ganglioneuroblastoma
Homo sapiens (human)
DOID:0110552
  • autosomal dominant nonsyndromic deafness 22
  • Aliases:
    • DFNA22
    • autosomal dominant deafness 22
Homo sapiens (human)
DOID:3981
  • pantothenate kinase-associated neurodegeneration
  • Aliases:
    • Hallervorden-Spatz disease
    • Hallervorden-Spatz syndrome
    • NBIA1
    • Pigmentary pallidal degeneration
    • brain Iron Accumulation type I syndrome
    • neurodegeneration with brain iron accumulation 1
Homo sapiens (human)
DOID:0111223
  • centronuclear myopathy 1
  • Aliases:
    • CNM1
Homo sapiens (human)
DOID:12678
  • hypercalcemia
Homo sapiens (human)
DOID:0060768
  • Smith-Magenis syndrome
  • Aliases:
    • 17p11.2 microdeletion syndrome
    • chromosome 17p11.2 deletion syndrome
Homo sapiens (human)
DOID:0111271
  • Oliver-McFarlane syndrome
  • Aliases:
    • OMCS
    • eyelashes long mental retardation
    • long eyelashes-intellectual disability syndrome
    • trichomegaly-retina pigmentary degeneration-dwarfism syndrome
Homo sapiens (human)
DOID:711
  • refractory hairy cell leukemia
Homo sapiens (human)
DOID:0050693
  • Brooke-Spiegler syndrome
  • Aliases:
    • BRSS
    • BSS
    • CYLD cutaneous syndrome
    • SBS
    • Spiegler-Brooke Syndrome
Homo sapiens (human)
DOID:0111344
  • myeloproliferative disorder with eosinophilia
  • Aliases:
    • chronic myeloproliferative disorder with eosinophilia
Homo sapiens (human)
DOID:854
  • collagen disease
  • Aliases:
    • collagen disorder
Homo sapiens (human)
DOID:11219
  • conjunctival folliculosis
  • Aliases:
    • acute follicular conjunctivitis
Homo sapiens (human)
DOID:0110437
  • dilated cardiomyopathy 1K
  • Aliases:
    • CMD1K
Homo sapiens (human)
DOID:0110203
  • Charcot-Marie-Tooth disease recessive intermediate D
  • Aliases:
    • CMTRID
    • RI-CMT type D
    • autosomal recessive intermediate Charcot-Marie-Tooth disease type D
Homo sapiens (human)
DOID:5495
  • monophasic synovial sarcoma
  • Aliases:
    • Monophasic sarcoma of Synovium
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