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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 9801 - 9825 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Organism Source
DOID:3324
  • mood disorder
  • Aliases:
    • episodic mood disorder
Caenorhabditis elegans
DOID:8866
  • actinic keratosis
  • Aliases:
    • SK - Solar keratosis
    • Senile hyperkeratosis
    • Solar keratosis
    • actinic (Solar) Keratosis
Mus musculus (house mouse)
DOID:2566
  • corneal dystrophy
Caenorhabditis elegans
DOID:0060287
  • cornea plana
  • Aliases:
    • flat cornea
Caenorhabditis elegans
DOID:3087
  • gingivitis
  • Aliases:
    • acute gingivitis
    • chronic gingivitis
Caenorhabditis elegans
DOID:11342
  • arcus senilis
  • Aliases:
    • Arcus of cornea
    • corneal arcus
Caenorhabditis elegans
DOID:0110474
  • autosomal recessive nonsyndromic deafness 18B
  • Aliases:
    • DFNB18B
    • autosomal recessive deafness 18B
Mus musculus (house mouse)
DOID:0080930
  • primary localized cutaneous amyloidosis 1
  • Aliases:
    • familial primary localized cutaneous amyloidosis-1
Mus musculus (house mouse)
DOID:0081366
  • Paget's disease of bone 3
  • Aliases:
    • Paget disease of bone-3
Mus musculus (house mouse)
DOID:0110068
  • frontotemporal dementia and/or amyotrophic lateral sclerosis 3
  • Aliases:
    • FTDALS3
Mus musculus (house mouse)
DOID:0081364
  • neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset
Mus musculus (house mouse)
DOID:0081363
  • distal myopathy with rimmed vacuoles
Mus musculus (house mouse)
DOID:0081368
  • Paget's disease of bone 5
  • Aliases:
    • Familial osteoectasia
    • Hereditary hyperphosphatasia
    • Hyperostosis corticalis deformans juvenilis
    • Juvenile Paget disease
    • Paget disease of bone-5
Mus musculus (house mouse)
DOID:0111582
  • hereditary arterial and articular multiple calcification syndrome
  • Aliases:
    • CALJA
    • arterial calcification and distal joint calcification
    • arterial calcification due to CD73 deficiency
    • arterial calcification due to deficiency of CD73
    • calcification of joints and arteries
Mus musculus (house mouse)
DOID:5408
  • Paget's disease of bone
  • Aliases:
    • Paget disease of bone
    • Paget's bone disease
    • osseous Paget's disease
    • osteitis deformans
Mus musculus (house mouse)
DOID:13948
  • bladder neck obstruction
  • Aliases:
    • Obstruction of bladder neck or vesicourethral orifice
Caenorhabditis elegans
DOID:14687
  • diastrophic dysplasia
Homo sapiens (human)
DOID:2300
  • spondylolysis
Homo sapiens (human)
DOID:0080055
  • achondrogenesis type IB
  • Aliases:
    • achondrogenesis Fraccaro type
Homo sapiens (human)
DOID:0070300
  • multiple epiphyseal dysplasia 4
  • Aliases:
    • EDM4
    • MED4
    • Polyepiphyseal dysplasia type 4
    • multiple epiphyseal dysplasia with bilateral patellae
    • multiple epiphyseal dysplasia with clubfoot
    • rMED
Homo sapiens (human)
DOID:0050581
  • brachydactyly
Homo sapiens (human)
DOID:0050648
  • atelosteogenesis
Homo sapiens (human)
DOID:0110076
  • arrhythmogenic right ventricular dysplasia 8
  • Aliases:
    • ARVC8
    • ARVD8
    • arrhythmogenic right ventricular cardiomyopathy 8
    • familial arrhythmogenic right ventricular dysplasia 8
Homo sapiens (human)
DOID:0090128
  • Carvajal syndrome
  • Aliases:
    • DCWHK
    • dilated cardiomyopathy with woolly hair and keratoderma
    • palmoplantar keratoderma with left ventricular cardiomyopathy and woolly hair
Homo sapiens (human)
DOID:0081109
  • keratosis palmoplantaris striata 2
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