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 1426 - 1450 of 4621 in total
Disease ID Disease Name ▲ Gene Symbol Gene ID Organism
DOID:0050700
  • cardiomyopathy
  • Aliases:
    • Cardiomyopathies
Homo sapiens (human)
DOID:1287
  • cardiovascular system disease
  • Aliases:
    • disease of subdivision of hemolymphoid system
Homo sapiens (human)
DOID:0090129
  • carnitine palmitoyltransferase I deficiency
  • Aliases:
    • CPT I deficiency
    • CPT1A deficiency
    • L-CPT1 deficiency
    • carnitine palmitoyl transferase 1A deficiency
    • carnitine palmitoyl transferase IA deficiency
    • hepatic CPT deficiency type I
    • hepatic carnitine palmitoyl transferase 1 deficiency
    • hepatic carnitine palmitoyl transferase I deficiency
Homo sapiens (human)
DOID:0060235
  • carnitine palmitoyltransferase II deficiency
  • Aliases:
    • CPT-II
    • infantile carnitine palmitoyltransferase II deficiency
    • late-onset carnitine palmitoyltransferase II deficiency
    • lethal neonatal carnitine palmitoyltransferase II deficiency
Homo sapiens (human)
DOID:3407
  • carotid artery disease
  • Aliases:
    • disorder of carotid artery
Homo sapiens (human)
DOID:3410
  • carotid artery thrombosis
Homo sapiens (human)
DOID:13001
  • carotid stenosis
  • Aliases:
    • Carotid artery stenosis
    • Stenosis, carotid artery
Homo sapiens (human)
DOID:12169
  • carpal tunnel syndrome
  • Aliases:
    • CTS - Carpal tunnel syndrome
    • Median nerve entrapment
    • carpal tunnel median neuropathy
Homo sapiens (human)
DOID:1222
  • cartilage disease
  • Aliases:
    • Cartilage disorder
    • Chondropathy
Homo sapiens (human)
DOID:14773
  • cartilage-hair hypoplasia
  • Aliases:
    • CHH
    • McKusick type metaphyseal chondrodysplasia
    • Metaphyseal chondrodysplasia, McKusick type
Homo sapiens (human)
DOID:0080909
  • castration-resistant prostate carcinoma
Homo sapiens (human)
DOID:11258
  • cat-scratch disease
  • Aliases:
    • Debre's Syndrome
    • Debre-Mollaret Syndrome
    • Foshay-Mollaret Cat Scratch Fever
    • benign lymphoreticulosis
    • cat scratch fever
Homo sapiens (human)
DOID:0110231
  • cataract 1 multiple types
  • Aliases:
    • CTRCT1
    • Duffy linked cataract
    • cataract 1, multiple types, with or without microcornea
Homo sapiens (human)
DOID:0110258
  • cataract 10 multiple types
  • Aliases:
    • CTRCT10
Homo sapiens (human)
DOID:0110249
  • cataract 11 multiple types
  • Aliases:
    • CTRCT11
Homo sapiens (human)
DOID:0110239
  • cataract 12 multiple types
  • Aliases:
    • CTRCT12
Homo sapiens (human)
DOID:0110242
  • cataract 13 with adult i phenotype
  • Aliases:
    • CTRCT13
Homo sapiens (human)
DOID:0110253
  • cataract 14 multiple types
  • Aliases:
    • CTRCT14
Homo sapiens (human)
DOID:0110251
  • cataract 15 multiple types
  • Aliases:
    • CTRCT15
Homo sapiens (human)
DOID:0110250
  • cataract 16 multiple types
  • Aliases:
    • CTRCT16
Homo sapiens (human)
DOID:0110270
  • cataract 17 multiple types
  • Aliases:
    • CTRCT17
Homo sapiens (human)
DOID:0110238
  • cataract 18
  • Aliases:
    • CATC2
    • CTRCT18
    • autosomal recessive congenital cataract 2
    • cataract 18 autosomal recessive
Homo sapiens (human)
DOID:0110263
  • cataract 19 multiple types
  • Aliases:
    • CTRCT19
Homo sapiens (human)
DOID:0110235
  • cataract 2 multiple types
  • Aliases:
    • CTRCT2
    • cataract 2 multiple types with or without microcornea
Homo sapiens (human)
DOID:0110240
  • cataract 20 multiple types
  • Aliases:
    • CTRCT20
Homo sapiens (human)

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International Collaboration

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