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 8901 - 8925 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source ▼
DOID:0111193
  • facioscapulohumeral muscular dystrophy 2
  • Aliases:
    • FSHD2
    • facioscapulohumeral muscular dystrophy 1B
    • facioscapulohumeral muscular dystrophy type 2
Homo sapiens (human)
DOID:0111190
  • distal myopathy 4
  • Aliases:
    • MPD4
    • distal ABD-filaminopathy
    • distal muscular dystrophy 4
    • distal myopathy with posterior leg and anterior hand involvement
Mus musculus (house mouse)
DOID:0111190
  • distal myopathy 4
  • Aliases:
    • MPD4
    • distal ABD-filaminopathy
    • distal muscular dystrophy 4
    • distal myopathy with posterior leg and anterior hand involvement
Homo sapiens (human)
DOID:0111189
  • distal myopathy 3
  • Aliases:
    • MPD3
    • distal muscular dystrophy 3
    • distal myopathy type 3
Mus musculus (house mouse)
DOID:0111189
  • distal myopathy 3
  • Aliases:
    • MPD3
    • distal muscular dystrophy 3
    • distal myopathy type 3
Homo sapiens (human)
DOID:0111188
  • myofibrillar myopathy 9
  • Aliases:
    • Edstrom myopathy
    • HIBM-ERF
    • HMERF
    • Hereditary inclusion body myopathy with early respiratory failure
    • MFM-titinopathy
    • MFM9
    • MPRM
    • Myofibrillar myopathy-titinopathy
    • autosomal dominant distal myopathy with early respiratory failure
    • hereditary myopathy with early respiratory failure
    • myofibrillar myopathy 9 with early respiratory failure
    • proximal myopathy with early respiratory muscle involvement
Homo sapiens (human)
DOID:0111188
  • myofibrillar myopathy 9
  • Aliases:
    • Edstrom myopathy
    • HIBM-ERF
    • HMERF
    • Hereditary inclusion body myopathy with early respiratory failure
    • MFM-titinopathy
    • MFM9
    • MPRM
    • Myofibrillar myopathy-titinopathy
    • autosomal dominant distal myopathy with early respiratory failure
    • hereditary myopathy with early respiratory failure
    • myofibrillar myopathy 9 with early respiratory failure
    • proximal myopathy with early respiratory muscle involvement
Mus musculus (house mouse)
DOID:0111187
  • distal myopathy with anterior tibial onset
  • Aliases:
    • DMAT
    • distal muscular dystrophy with anterior tibial onset
Mus musculus (house mouse)
DOID:0111186
  • myopathy, lactic acidosis, and sideroblastic anemia 2
  • Aliases:
    • MLASA2
Homo sapiens (human)
DOID:0111183
  • familial hemiplegic migraine 3
  • Aliases:
    • FHM3
    • MHP3
Rattus norvegicus (Norway rat)
DOID:0111183
  • familial hemiplegic migraine 3
  • Aliases:
    • FHM3
    • MHP3
Drosophila melanogaster (fruit fly)
DOID:0111183
  • familial hemiplegic migraine 3
  • Aliases:
    • FHM3
    • MHP3
Mus musculus (house mouse)
DOID:0111183
  • familial hemiplegic migraine 3
  • Aliases:
    • FHM3
    • MHP3
Homo sapiens (human)
DOID:0111182
  • familial hemiplegic migraine 2
  • Aliases:
    • FHM2
    • Familial hemiplegic migraine-2
    • MHP2
Rattus norvegicus (Norway rat)
DOID:0111182
  • familial hemiplegic migraine 2
  • Aliases:
    • FHM2
    • Familial hemiplegic migraine-2
    • MHP2
Mus musculus (house mouse)
DOID:0111182
  • familial hemiplegic migraine 2
  • Aliases:
    • FHM2
    • Familial hemiplegic migraine-2
    • MHP2
Homo sapiens (human)
DOID:0111182
  • familial hemiplegic migraine 2
  • Aliases:
    • FHM2
    • Familial hemiplegic migraine-2
    • MHP2
Drosophila melanogaster (fruit fly)
DOID:0111181
  • familial hemiplegic migraine 1
  • Aliases:
    • FHM1
    • MHP1
    • familial hemiplegic migraine1 with progressive cerebellar ataxia
Drosophila melanogaster (fruit fly)
DOID:0111181
  • familial hemiplegic migraine 1
  • Aliases:
    • FHM1
    • MHP1
    • familial hemiplegic migraine1 with progressive cerebellar ataxia
Mus musculus (house mouse)
DOID:0111181
  • familial hemiplegic migraine 1
  • Aliases:
    • FHM1
    • MHP1
    • familial hemiplegic migraine1 with progressive cerebellar ataxia
Homo sapiens (human)
DOID:0111181
  • familial hemiplegic migraine 1
  • Aliases:
    • FHM1
    • MHP1
    • familial hemiplegic migraine1 with progressive cerebellar ataxia
Danio rerio (zebrafish)
DOID:0111181
  • familial hemiplegic migraine 1
  • Aliases:
    • FHM1
    • MHP1
    • familial hemiplegic migraine1 with progressive cerebellar ataxia
Rattus norvegicus (Norway rat)
DOID:0111180
  • French Canadian Leigh disease
  • Aliases:
    • French Canadian type COX deficiency
    • French Canadian type Leigh syndrome
    • French Canadian type cytochrome c oxidase deficiency
    • Saguenay Lac saint Jean type COX deficiency
    • Saguenay Lac saint Jean type Leigh syndrome
    • mitochondrial complex IV deficiency nuclear type 5
Mus musculus (house mouse)
DOID:0111180
  • French Canadian Leigh disease
  • Aliases:
    • French Canadian type COX deficiency
    • French Canadian type Leigh syndrome
    • French Canadian type cytochrome c oxidase deficiency
    • Saguenay Lac saint Jean type COX deficiency
    • Saguenay Lac saint Jean type Leigh syndrome
    • mitochondrial complex IV deficiency nuclear type 5
Homo sapiens (human)
DOID:0111169
  • subcortical band heterotopia
  • Aliases:
    • HeCo
    • band heterotopia
    • double cortex syndrome
    • heterotopic cortex
    • subcortical laminar heterotopia
Mus musculus (house mouse)

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Supported by JST NBDC Grant Number JPMJND2204

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Last updated: December 9, 2024