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 2251 - 2275 of 15957 in total
Disease ID Disease Name ▼ Gene Symbol Gene ID Organism Source
DOID:0111535
  • progressive osseous heteroplasia
  • Aliases:
    • POH
    • ectopic ossification familial type
    • familial ectopic ossification
    • osteoma cutis
Xenopus laevis (African clawed frog)
DOID:0111535
  • progressive osseous heteroplasia
  • Aliases:
    • POH
    • ectopic ossification familial type
    • familial ectopic ossification
    • osteoma cutis
Rattus norvegicus (Norway rat)
DOID:0111535
  • progressive osseous heteroplasia
  • Aliases:
    • POH
    • ectopic ossification familial type
    • familial ectopic ossification
    • osteoma cutis
Homo sapiens (human)
DOID:0111535
  • progressive osseous heteroplasia
  • Aliases:
    • POH
    • ectopic ossification familial type
    • familial ectopic ossification
    • osteoma cutis
Drosophila melanogaster (fruit fly)
DOID:0111535
  • progressive osseous heteroplasia
  • Aliases:
    • POH
    • ectopic ossification familial type
    • familial ectopic ossification
    • osteoma cutis
Caenorhabditis elegans
DOID:891
  • progressive myoclonus epilepsy
  • Aliases:
    • PME
    • progressive myoclonic epilepsy
Homo sapiens (human)
DOID:891
  • progressive myoclonus epilepsy
  • Aliases:
    • PME
    • progressive myoclonic epilepsy
Mus musculus (house mouse)
DOID:891
  • progressive myoclonus epilepsy
  • Aliases:
    • PME
    • progressive myoclonic epilepsy
Rattus norvegicus (Norway rat)
DOID:891
  • progressive myoclonus epilepsy
  • Aliases:
    • PME
    • progressive myoclonic epilepsy
Caenorhabditis elegans
DOID:891
  • progressive myoclonus epilepsy
  • Aliases:
    • PME
    • progressive myoclonic epilepsy
Drosophila melanogaster (fruit fly)
DOID:0111450
  • progressive myoclonus epilepsy 9
  • Aliases:
    • EMP9
    • PME type 9
    • progressive myoclonic epilepsy due to LMNB2 deficiency
    • progressive myoclonus epilepsy type 9
Mus musculus (house mouse)
DOID:0111450
  • progressive myoclonus epilepsy 9
  • Aliases:
    • EMP9
    • PME type 9
    • progressive myoclonic epilepsy due to LMNB2 deficiency
    • progressive myoclonus epilepsy type 9
Homo sapiens (human)
DOID:0111451
  • progressive myoclonus epilepsy 8
  • Aliases:
    • EMP8
    • PME type 8
    • progressive myoclonic epilepsy due to CERS1 deficiency
    • progressive myoclonus epilepsy type 8
Saccharomyces cerevisiae S288C
DOID:0111451
  • progressive myoclonus epilepsy 8
  • Aliases:
    • EMP8
    • PME type 8
    • progressive myoclonic epilepsy due to CERS1 deficiency
    • progressive myoclonus epilepsy type 8
Homo sapiens (human)
DOID:0111447
  • progressive myoclonus epilepsy 7
  • Aliases:
    • EPM7
    • MEAK
    • Myoclonus epilepsy and ataxia due to potassium channel mutation
    • PME type 7
    • Progressive myoclonic epilepsy due to KV3.1 deficiency
    • Progressive myoclonus epilepsy type 7
Drosophila melanogaster (fruit fly)
DOID:0111447
  • progressive myoclonus epilepsy 7
  • Aliases:
    • EPM7
    • MEAK
    • Myoclonus epilepsy and ataxia due to potassium channel mutation
    • PME type 7
    • Progressive myoclonic epilepsy due to KV3.1 deficiency
    • Progressive myoclonus epilepsy type 7
Homo sapiens (human)
DOID:0111447
  • progressive myoclonus epilepsy 7
  • Aliases:
    • EPM7
    • MEAK
    • Myoclonus epilepsy and ataxia due to potassium channel mutation
    • PME type 7
    • Progressive myoclonic epilepsy due to KV3.1 deficiency
    • Progressive myoclonus epilepsy type 7
Mus musculus (house mouse)
DOID:0111447
  • progressive myoclonus epilepsy 7
  • Aliases:
    • EPM7
    • MEAK
    • Myoclonus epilepsy and ataxia due to potassium channel mutation
    • PME type 7
    • Progressive myoclonic epilepsy due to KV3.1 deficiency
    • Progressive myoclonus epilepsy type 7
Rattus norvegicus (Norway rat)
DOID:0111444
  • progressive myoclonus epilepsy 4
  • Aliases:
    • AMRF
    • EPM4
    • Myoclonus-nephropathy syndrome
    • action myoclonus-renal failure syndrome
Homo sapiens (human)
DOID:0111444
  • progressive myoclonus epilepsy 4
  • Aliases:
    • AMRF
    • EPM4
    • Myoclonus-nephropathy syndrome
    • action myoclonus-renal failure syndrome
Rattus norvegicus (Norway rat)
DOID:0111444
  • progressive myoclonus epilepsy 4
  • Aliases:
    • AMRF
    • EPM4
    • Myoclonus-nephropathy syndrome
    • action myoclonus-renal failure syndrome
Mus musculus (house mouse)
DOID:0111444
  • progressive myoclonus epilepsy 4
  • Aliases:
    • AMRF
    • EPM4
    • Myoclonus-nephropathy syndrome
    • action myoclonus-renal failure syndrome
Caenorhabditis elegans
DOID:0111446
  • progressive myoclonus epilepsy 3
  • Aliases:
    • CLN14 disease
    • EPM3
    • PME type 3
    • Progressive myoclonic epilepsy due to KCTD7 deficiency
    • Progressive myoclonus epilepsy type 3
    • neuronal ceroid lipofuscinosis 14
Homo sapiens (human)
DOID:0111446
  • progressive myoclonus epilepsy 3
  • Aliases:
    • CLN14 disease
    • EPM3
    • PME type 3
    • Progressive myoclonic epilepsy due to KCTD7 deficiency
    • Progressive myoclonus epilepsy type 3
    • neuronal ceroid lipofuscinosis 14
Saccharomyces cerevisiae S288C
DOID:0111448
  • progressive myoclonus epilepsy 1B
  • Aliases:
    • EPM1B
Homo sapiens (human)

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Last updated: December 9, 2024