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 5276 - 5300 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Organism Source
DOID:4676
  • uremia
  • Aliases:
    • UREMIA OF renal ORIGIN
Caenorhabditis elegans
DOID:767
  • muscular atrophy
  • Aliases:
    • Amyotrophia
    • Muscle wasting
    • Wasting - muscle
Caenorhabditis elegans
DOID:0111072
  • myostatin-related muscle hypertrophy
  • Aliases:
    • MSLHP
Caenorhabditis elegans
DOID:0070418
  • vertebral hypersegmentation and orofacial anomalies
  • Aliases:
    • VHO
Caenorhabditis elegans
DOID:0050540
  • Charcot-Marie-Tooth disease type 3
  • Aliases:
    • DEJERINE-SOTTAS NEUROPATHY
    • DEJERINE-SOTTAS SYNDROME
Mus musculus (house mouse)
DOID:0110152
  • Charcot-Marie-Tooth disease type 1B
  • Aliases:
    • CMT1B
    • Charcot-Marie-Tooth disease slow nerve conduction type linked to Duffy
    • Charcot-Marie-Tooth neuropathy type 1B
    • HMSN IB
    • HMSN1B
    • autosomal dominant Charcot-Marie-Tooth disease with focally folded myelin sheaths type 1B
    • hereditary motor and sensory neuropathy IB
    • peroneal muscular atrophy
Mus musculus (house mouse)
DOID:0090111
  • PCWH syndrome
  • Aliases:
    • Neurologic Waardenburg-Shah syndrome
    • PCWH
    • Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease
    • Peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Hirschsprung disease-Waardenburg syndrome
Mus musculus (house mouse)
DOID:0110157
  • Charcot-Marie-Tooth disease type 2J
  • Aliases:
    • CMT2J
    • Charcot-Marie-Tooth disease type 2 with hearing loss and pupillary abnormalities
    • Charcot-Marie-Tooth neuropathy type 2J
Mus musculus (house mouse)
DOID:0110158
  • Charcot-Marie-Tooth disease type 2I
  • Aliases:
    • CMT2I
    • Charcot-Marie-Tooth neuropathy type 2I
Mus musculus (house mouse)
DOID:0110200
  • Charcot-Marie-Tooth disease dominant intermediate D
  • Aliases:
    • CMTDID
    • Charcot-Marie-Tooth neuropathy dominant intermediate D
    • DI-CMTD
    • autosomal dominant intermediate Charcot-Marie-Tooth disease type D
Mus musculus (house mouse)
DOID:557
  • kidney disease
  • Aliases:
    • impaired renal function disease
    • nephropathy
Caenorhabditis elegans
DOID:1825
  • childhood absence epilepsy
  • Aliases:
    • petit mal seizure
    • pyknolepsy
Caenorhabditis elegans
DOID:10941
  • intracranial aneurysm
  • Aliases:
    • brain aneurysm
Caenorhabditis elegans
DOID:9477
  • pulmonary embolism
  • Aliases:
    • pulmonary artery embolism
    • pulmonary embolus
Caenorhabditis elegans
DOID:13580
  • cholestasis
  • Aliases:
    • Obstruction of bile duct
    • bile occlusion
Caenorhabditis elegans
DOID:11612
  • polycystic ovary syndrome
  • Aliases:
    • Multicystic ovaries
    • PCOS
    • Polycystic Ovarian disease
    • Polycystic ovaries
    • Stein-Leventhal synd.
    • Stein-Leventhal syndrome
    • polycystic ovary
Caenorhabditis elegans
DOID:9282
  • ocular hypertension
Caenorhabditis elegans
DOID:824
  • periodontitis
  • Aliases:
    • chronic pericementitis
Caenorhabditis elegans
DOID:0080176
  • meningococcal meningitis
Caenorhabditis elegans
DOID:13139
  • crescentic glomerulonephritis
Caenorhabditis elegans
DOID:4724
  • brain edema
  • Aliases:
    • intracranial swelling
    • wet brain
Caenorhabditis elegans
DOID:1073
  • renal hypertension
Caenorhabditis elegans
DOID:0050851
  • glomerulosclerosis
Caenorhabditis elegans
DOID:12510
  • retinal ischemia
Caenorhabditis elegans
DOID:6195
  • conjunctivitis
Caenorhabditis elegans

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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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