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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 12826 - 12850 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source ▼
DOID:0070505
  • mitochondrial complex IV deficiency nuclear type 20
  • Aliases:
    • MC4DN20
Rattus norvegicus (Norway rat)
DOID:0070501
  • mitochondrial complex IV deficiency nuclear type 16
  • Aliases:
    • MC4DN16
Rattus norvegicus (Norway rat)
DOID:0070501
  • mitochondrial complex IV deficiency nuclear type 16
  • Aliases:
    • MC4DN16
Mus musculus (house mouse)
DOID:0070495
  • mitochondrial complex IV deficiency nuclear type 8
  • Aliases:
    • MC4DN8
Homo sapiens (human)
DOID:0070494
  • mitochondrial complex IV deficiency nuclear type 7
  • Aliases:
    • MC4DN7
Mus musculus (house mouse)
DOID:0070491
  • mitochondrial complex IV deficiency nuclear type 1
  • Aliases:
    • MC4DN1
Homo sapiens (human)
DOID:0070490
  • infantile parkinsonism-dystonia 2
  • Aliases:
    • Brain dopamine-serotonin vesicular transport disease
    • PKDYS2
Caenorhabditis elegans
DOID:0070490
  • infantile parkinsonism-dystonia 2
  • Aliases:
    • Brain dopamine-serotonin vesicular transport disease
    • PKDYS2
Rattus norvegicus (Norway rat)
DOID:0070490
  • infantile parkinsonism-dystonia 2
  • Aliases:
    • Brain dopamine-serotonin vesicular transport disease
    • PKDYS2
Mus musculus (house mouse)
DOID:0070490
  • infantile parkinsonism-dystonia 2
  • Aliases:
    • Brain dopamine-serotonin vesicular transport disease
    • PKDYS2
Homo sapiens (human)
DOID:0070489
  • classic dopamine transporter deficiency syndrome
  • Aliases:
    • PKDYS1
    • classic DTDS
    • infantile parkinsonism-dystonia 1
Homo sapiens (human)
DOID:0070489
  • classic dopamine transporter deficiency syndrome
  • Aliases:
    • PKDYS1
    • classic DTDS
    • infantile parkinsonism-dystonia 1
Drosophila melanogaster (fruit fly)
DOID:0070489
  • classic dopamine transporter deficiency syndrome
  • Aliases:
    • PKDYS1
    • classic DTDS
    • infantile parkinsonism-dystonia 1
Mus musculus (house mouse)
DOID:0070489
  • classic dopamine transporter deficiency syndrome
  • Aliases:
    • PKDYS1
    • classic DTDS
    • infantile parkinsonism-dystonia 1
Rattus norvegicus (Norway rat)
DOID:0070489
  • classic dopamine transporter deficiency syndrome
  • Aliases:
    • PKDYS1
    • classic DTDS
    • infantile parkinsonism-dystonia 1
Caenorhabditis elegans
DOID:0070486
  • Parkinson's disease 25
  • Aliases:
    • PARK25
    • autosomal recessive early-onset Parkinson disease 25 with impaired intellectual development
Mus musculus (house mouse)
DOID:0070486
  • Parkinson's disease 25
  • Aliases:
    • PARK25
    • autosomal recessive early-onset Parkinson disease 25 with impaired intellectual development
Homo sapiens (human)
DOID:0070485
  • mitochondrial complex IV deficiency nuclear type 23
  • Aliases:
    • MC4DN23
Homo sapiens (human)
DOID:0070484
  • Legius syndrome
  • Aliases:
    • LGSS
    • NF1-like syndrome
    • neurofibromatosis type 1-like syndrome
Homo sapiens (human)
DOID:0070484
  • Legius syndrome
  • Aliases:
    • LGSS
    • NF1-like syndrome
    • neurofibromatosis type 1-like syndrome
Mus musculus (house mouse)
DOID:0070483
  • Watson syndrome
Mus musculus (house mouse)
DOID:0070483
  • Watson syndrome
Homo sapiens (human)
DOID:0070482
  • spinal neurofibromatosis
  • Aliases:
    • FNSF
    • SNF
    • familial spinal neurofibromatosis
Mus musculus (house mouse)
DOID:0070482
  • spinal neurofibromatosis
  • Aliases:
    • FNSF
    • SNF
    • familial spinal neurofibromatosis
Homo sapiens (human)
DOID:0070480
  • schwannomatosis 1
  • Aliases:
    • SMARCB1-related schwannomatosis
    • SWN1
Saccharomyces cerevisiae S288C
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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