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 4026 - 4050 of 4621 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼
DOID:0111350
  • Laurin-Sandrow syndrome
  • Aliases:
    • MIPduplication of fibuland ulna with absence of tibia and radius
    • Sandrow syndrome
    • TMIP
    • miccor hands and feet with nasal defects
    • mirror hands and feets-nasal defects syndrome
    • mirror-image polydactyly
    • tetramelic mirror-image polydactyly
Homo sapiens (human)
DOID:0050955
  • spinocerebellar ataxia type 2
Homo sapiens (human)
DOID:0110829
  • retinitis pigmentosa-deafness syndrome
Homo sapiens (human)
DOID:11130
  • secondary hypertension
Homo sapiens (human)
DOID:0110343
  • osteogenesis imperfecta type 14
  • Aliases:
    • OI14
    • osteogenesis imperfecta type XIV
Homo sapiens (human)
DOID:9766
  • xanthogranulomatous cholecystitis
Homo sapiens (human)
DOID:0050697
  • chorioamnionitis
Homo sapiens (human)
DOID:0050467
  • erythrokeratodermia variabilis
  • Aliases:
    • Erythrokeratodermia Figurata Variabilis
    • Greither Disease
Homo sapiens (human)
DOID:0080540
  • galactosialidosis
Homo sapiens (human)
DOID:9471
  • meningitis
Homo sapiens (human)
DOID:573
  • nerve compression syndrome
  • Aliases:
    • Compression neuropathy
    • entrapment neuropathy
    • peripheral nerve entrapment syndrome
Homo sapiens (human)
DOID:12961
  • Poland syndrome
  • Aliases:
    • Poland's syndactyly
Homo sapiens (human)
DOID:9279
  • hyperhomocysteinemia
Homo sapiens (human)
DOID:9277
  • primary cerebellar degeneration
Homo sapiens (human)
DOID:8577
  • ulcerative colitis
  • Aliases:
    • Left-sided ulcerative colitis
Homo sapiens (human)
DOID:0110221
  • Brugada syndrome 4
  • Aliases:
    • BRGDA4
Homo sapiens (human)
DOID:1800
  • neuroendocrine carcinoma
Homo sapiens (human)
DOID:0080501
  • GM1 gangliosidosis type 2
  • Aliases:
    • juvenile GM1 gangliosidosis
Homo sapiens (human)
DOID:0060488
  • Pitt-Hopkins syndrome
Homo sapiens (human)
DOID:14448
  • 46,XY sex reversal
  • Aliases:
    • 46 XY gonadal dysgenesis
    • Pure gonadal dysgenesis 46,XY
    • Swyer syndrome
Homo sapiens (human)
DOID:9505
  • cannabis abuse
  • Aliases:
    • marijuana abuse
Homo sapiens (human)
DOID:2536
  • chronic inflammatory demyelinating polyneuritis
Homo sapiens (human)
DOID:0110292
  • autosomal recessive limb-girdle muscular dystrophy type 2O
  • Aliases:
    • LGMD2O
    • MDDGC3
    • muscular dystrophy-dystroglycanopathy (limb-girdle) type C3
    • muscular dystrophy-dystroglycanopathy limb-girdle POMGNT1-related
Homo sapiens (human)
DOID:0110256
  • cataract 21 multiple types
  • Aliases:
    • CTRCT21
    • cataract 21 multiple types with or without microcornea
Homo sapiens (human)
DOID:0060452
  • posterior amorphous corneal dystrophy
  • Aliases:
    • PACD
    • chromosome 12q21.33 deletion syndrome
Homo sapiens (human)

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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