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 1501 - 1525 of 4649 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source ▼
DOID:1192
  • peripheral nervous system neoplasm
  • Aliases:
    • neoplasm of peripheral nerve
    • nerve sheath neoplasm
    • tumor of PNS
Homo sapiens (human)
DOID:1188
  • mononeuropathy
Homo sapiens (human)
DOID:11870
  • Pick's disease
  • Aliases:
    • Dementia in Pick's disease
    • LOBAR ATROPHY OF BRAIN
    • PICK DISEASE OF BRAIN
    • Pick disease
Homo sapiens (human)
DOID:11847
  • coronary thrombosis
  • Aliases:
    • Coronary artery thrombosis
Homo sapiens (human)
DOID:1184
  • nephrotic syndrome
Homo sapiens (human)
DOID:11836
  • clubfoot
  • Aliases:
    • Congenital equinovarus
    • Equinovarus deformity of foot
    • congenital clubfoot
    • congenital talipes equinovarus
Homo sapiens (human)
DOID:11832
  • visual epilepsy
  • Aliases:
    • epilepsy, visual
Homo sapiens (human)
DOID:11830
  • myopia
  • Aliases:
    • near vision
    • near-sightedness
    • short-sightedness
Homo sapiens (human)
DOID:11829
  • degenerative myopia
  • Aliases:
    • degenerative progressive high myopia
    • pathological myopia
    • progressive high (degenerative) myopia
    • progressive high myopia
Homo sapiens (human)
DOID:11823
  • hepatorenal syndrome
Homo sapiens (human)
DOID:11801
  • protein-energy malnutrition
Homo sapiens (human)
DOID:118
  • pericardial effusion
Homo sapiens (human)
DOID:11759
  • hypochromic anemia
  • Aliases:
    • ANEMIA HYPOCHROMIC
Homo sapiens (human)
DOID:11758
  • iron deficiency anemia
Homo sapiens (human)
DOID:11729
  • Lyme disease
  • Aliases:
    • Bannwarth syndrome
    • Bannworth's syndrome
    • Lyme borreliosis
    • Neurological Lyme disease
    • lyme neuroborreliosis
    • neuroborreliosis
Homo sapiens (human)
DOID:11727
  • facioscapulohumeral muscular dystrophy
  • Aliases:
    • Landouzy Dejerine muscular dystrophy
    • Landouzy-Dejerine muscular dystrophy
    • Muscular dystrophy, Landouzy-Dejerine
Homo sapiens (human)
DOID:11726
  • Emery-Dreifuss muscular dystrophy
  • Aliases:
    • EDMD
Homo sapiens (human)
DOID:11725
  • Cornelia de Lange syndrome
  • Aliases:
    • Brachmann de Lange syndrome
    • De Lange syndrome
Homo sapiens (human)
DOID:11724
  • limb-girdle muscular dystrophy
  • Aliases:
    • Erb's muscular dystrophy
    • Leyden-Mbius muscular dystrophy
    • limb girdle muscular dystrophy
Homo sapiens (human)
DOID:11722
  • myotonic dystrophy type 1
  • Aliases:
    • Dystrophia myotonica
    • Steinert disease
    • congenital myotonic dystrophy
    • myotonic dystrophy of Steinert
Homo sapiens (human)
DOID:11721
  • glycogen storage disease VII
  • Aliases:
    • Glycogen storage disease 7
    • Glycogen storage disease, type VII
    • Muscle phosphofructokinase deficiency
    • glycogen storage disease type VII
    • phosphofructokinase myopathy
Homo sapiens (human)
DOID:11720
  • distal myopathy
  • Aliases:
    • distal muscular dystrophy
Homo sapiens (human)
DOID:1172
  • hyperlipoproteinemia type IV
  • Aliases:
    • Endogenous hyperlipidaemia
    • Fredrickson type IV Lipidemia
    • Fredrickson type IV hyperlipoproteinemia
    • Fredrickson type IV lipidaemia
    • VLDL hyperlipoproteinemia
    • familial hypertriglyceridemia
Homo sapiens (human)
DOID:11719
  • oculopharyngeal muscular dystrophy
  • Aliases:
    • Muscular dystrophy, oculopharyngeal
Homo sapiens (human)
DOID:11717
  • neonatal diabetes
  • Aliases:
    • diabetes mellitus syndrome in newborn infant
    • neonatal diabetes mellitus
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