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 12801 - 12825 of 15957 in total
Disease ID ▼ Disease Name Gene Symbol Gene ID Organism Source
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
DOID:0070480
  • schwannomatosis 1
  • Aliases:
    • SMARCB1-related schwannomatosis
    • SWN1
Homo sapiens (human)
DOID:0070478
  • diphthamide deficiency syndrome 2
  • Aliases:
    • DEDSSH2
    • developmental delay with short stature, dysmorphic facial features, and sparse hair 2
Homo sapiens (human)
DOID:0070478
  • diphthamide deficiency syndrome 2
  • Aliases:
    • DEDSSH2
    • developmental delay with short stature, dysmorphic facial features, and sparse hair 2
Mus musculus (house mouse)
DOID:0070476
  • diphthamide deficiency syndrome
  • Aliases:
    • DEDSSH
    • craniofacial dysplasia-short stature-ectodermal anomalies-intellectual disability syndrome
    • developmental delay with short stature, dysmorphic facial features, and sparse hair
Mus musculus (house mouse)
DOID:0070476
  • diphthamide deficiency syndrome
  • Aliases:
    • DEDSSH
    • craniofacial dysplasia-short stature-ectodermal anomalies-intellectual disability syndrome
    • developmental delay with short stature, dysmorphic facial features, and sparse hair
Homo sapiens (human)
DOID:0070474
  • childhood-onset neurodegeneration with brain atrophy
  • Aliases:
    • CONDBA
    • childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder
Homo sapiens (human)
DOID:0070473
  • Zaki syndrome
Caenorhabditis elegans
DOID:0070473
  • Zaki syndrome
Drosophila melanogaster (fruit fly)
DOID:0070473
  • Zaki syndrome
Homo sapiens (human)

About Release Notes Help Feedback

Click here to visit the beta site.


International Collaboration

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


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.1.0

Last updated: December 9, 2024