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 14876 - 14900 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Organism Source
DOID:1686
  • glaucoma
Mus musculus (house mouse)
DOID:0070398
  • hypomyelinating leukodystrophy 15
  • Aliases:
    • HLD15
Mus musculus (house mouse)
DOID:3389
  • Papillon-Lefevre disease
  • Aliases:
    • Papillon Lefevre syndrome
    • Papillon-Lefvre syndrome
Homo sapiens (human)
DOID:0050941
  • spastic ataxia 2
Homo sapiens (human)
DOID:863
  • nervous system disease
Homo sapiens (human)
DOID:0080547
  • metabolic dysfunction-associated steatohepatitis
  • Aliases:
    • MASH
    • NASH
    • non-alcoholic steatohepatitis
    • nonalcoholic steatohepatitis
Mus musculus (house mouse)
DOID:0060853
  • Potocki-Lupski syndrome
  • Aliases:
    • 17p11.2 microduplication syndrome
    • chromosome 17p11.2 duplication syndrome
    • trisomy 17p11.2
Homo sapiens (human)
DOID:0060768
  • Smith-Magenis syndrome
  • Aliases:
    • 17p11.2 microdeletion syndrome
    • chromosome 17p11.2 deletion syndrome
Homo sapiens (human)
DOID:0112350
  • spermatogenic failure 61
  • Aliases:
    • SPGF61
Homo sapiens (human)
DOID:0080865
  • primary ovarian insufficiency 8
Homo sapiens (human)
DOID:0110202
  • Charcot-Marie-Tooth disease dominant intermediate A
  • Aliases:
    • CMTDIA
    • Charcot-Marie-Tooth neuropathy dominant intermediate A
    • DI-CMTA
    • autosomal dominant intermediate Charcot-Marie-Tooth disease type A
Mus musculus (house mouse)
DOID:0111436
  • optic atrophy 11
  • Aliases:
    • OPA11
Homo sapiens (human)
DOID:3181
  • oligodendroglioma
  • Aliases:
    • oligodendroglial neoplasm
    • oligodendroglial tumor
Homo sapiens (human)
DOID:070355
  • multisystem proteinopathy
Mus musculus (house mouse)
DOID:0110199
  • Charcot-Marie-Tooth disease dominant intermediate C
  • Aliases:
    • CMTDIC
    • Charcot-Marie-Tooth neuropathy dominant intermediate C
    • DI-CMTC
    • autosomal dominant intermediate Charcot-Marie-Tooth disease type C
Mus musculus (house mouse)
DOID:870
  • neuropathy
  • Aliases:
    • peripheral neuropathy
Mus musculus (house mouse)
DOID:162
  • cancer
  • Aliases:
    • malignant neoplasm
    • malignant tumor
    • primary cancer
Mus musculus (house mouse)
DOID:10595
  • Charcot-Marie-Tooth disease
  • Aliases:
    • CMT - Charcot-Marie-Tooth disease
Mus musculus (house mouse)
DOID:0110934
  • nemaline myopathy 7
  • Aliases:
    • NEM7
    • nemaline myopathy 7, autosomal recessive
Homo sapiens (human)
DOID:11457
  • brain compression
Homo sapiens (human)
DOID:0050731
  • vitamin B12 deficiency
  • Aliases:
    • cobalamin deficiency
    • hypocobalaminemia
Homo sapiens (human)
DOID:4948
  • gallbladder carcinoma
  • Aliases:
    • cancer of the gallbladder
    • carcinoma gallbladder
    • carcinoma of gallbladder
Homo sapiens (human)
DOID:0050562
  • West syndrome
Homo sapiens (human)
DOID:1875
  • impotence
  • Aliases:
    • Sexual impotence
    • erectile dysfunction
Homo sapiens (human)
DOID:5199
  • ureteral obstruction
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: December 9, 2024