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 5401 - 5425 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source ▲
DOID:0110030
  • alpha thalassemia-X-linked intellectual disability syndrome
  • Aliases:
    • ATR, nondeletion type
    • ATR-X syndrome
    • alpha-thalassemia/mental retardation syndrome nondeletion type
Homo sapiens (human)
DOID:0110031
  • hemoglobin H disease
  • Aliases:
    • HBH
    • alpha thalassemia, haemoglobin H type
    • alpha thalassemia, hemoglobin H type
    • alpha-thalassemia intermedia
    • haemoglobin H disease
    • haemoglobin H disease, deletional
    • hemoglobin H disease, deletional
Homo sapiens (human)
DOID:0110032
  • autosomal dominant Alport syndrome
Mus musculus (house mouse)
DOID:0110032
  • autosomal dominant Alport syndrome
Drosophila melanogaster (fruit fly)
DOID:0110032
  • autosomal dominant Alport syndrome
Homo sapiens (human)
DOID:0110033
  • autosomal recessive Alport syndrome
Homo sapiens (human)
DOID:0110033
  • autosomal recessive Alport syndrome
Drosophila melanogaster (fruit fly)
DOID:0110033
  • autosomal recessive Alport syndrome
Mus musculus (house mouse)
DOID:0110033
  • autosomal recessive Alport syndrome
Caenorhabditis elegans
DOID:0110034
  • X-linked Alport syndrome
  • Aliases:
    • nephropathy and deafness, X-linked
Drosophila melanogaster (fruit fly)
DOID:0110034
  • X-linked Alport syndrome
  • Aliases:
    • nephropathy and deafness, X-linked
Homo sapiens (human)
DOID:0110034
  • X-linked Alport syndrome
  • Aliases:
    • nephropathy and deafness, X-linked
Caenorhabditis elegans
DOID:0110035
  • Alzheimer's disease 2
  • Aliases:
    • AD2
    • Alzheimer disease 2, late onset
    • Alzheimer disease associated with APOE4
    • Alzheimer disease-2
Homo sapiens (human)
DOID:0110040
  • Alzheimer's disease 4
  • Aliases:
    • AD4
    • Alzheimer disease 4
    • Alzheimer disease, familial4
    • Alzheimer's disease 4, early onset
Drosophila melanogaster (fruit fly)
DOID:0110040
  • Alzheimer's disease 4
  • Aliases:
    • AD4
    • Alzheimer disease 4
    • Alzheimer disease, familial4
    • Alzheimer's disease 4, early onset
Xenopus laevis (African clawed frog)
DOID:0110042
  • Alzheimer's disease 3
  • Aliases:
    • AD3
    • Alzheimer disease 3
    • Alzheimer disease 3, early onset
    • Alzheimer disease familial 3
Drosophila melanogaster (fruit fly)
DOID:0110042
  • Alzheimer's disease 3
  • Aliases:
    • AD3
    • Alzheimer disease 3
    • Alzheimer disease 3, early onset
    • Alzheimer disease familial 3
Homo sapiens (human)
DOID:0110042
  • Alzheimer's disease 3
  • Aliases:
    • AD3
    • Alzheimer disease 3
    • Alzheimer disease 3, early onset
    • Alzheimer disease familial 3
Xenopus laevis (African clawed frog)
DOID:0110050
  • Alzheimer's disease 18
  • Aliases:
    • AD18
    • Alzheimer disease 18
    • Alzheimer's disease 18, late onset
Rattus norvegicus (Norway rat)
DOID:0110050
  • Alzheimer's disease 18
  • Aliases:
    • AD18
    • Alzheimer disease 18
    • Alzheimer's disease 18, late onset
Xenopus laevis (African clawed frog)
DOID:0110050
  • Alzheimer's disease 18
  • Aliases:
    • AD18
    • Alzheimer disease 18
    • Alzheimer's disease 18, late onset
Homo sapiens (human)
DOID:0110050
  • Alzheimer's disease 18
  • Aliases:
    • AD18
    • Alzheimer disease 18
    • Alzheimer's disease 18, late onset
Caenorhabditis elegans
DOID:0110050
  • Alzheimer's disease 18
  • Aliases:
    • AD18
    • Alzheimer disease 18
    • Alzheimer's disease 18, late onset
Mus musculus (house mouse)
DOID:0110052
  • amelogenesis imperfecta type 1B
  • Aliases:
    • AI1B
    • AIH2
    • amelogenesis imperfecta type IB
    • autosomal dominant hypoplastic local amelogenesis imperfecta
    • hereditary localized enamel hypoplasia
Homo sapiens (human)
DOID:0110052
  • amelogenesis imperfecta type 1B
  • Aliases:
    • AI1B
    • AIH2
    • amelogenesis imperfecta type IB
    • autosomal dominant hypoplastic local amelogenesis imperfecta
    • hereditary localized enamel hypoplasia
Mus musculus (house mouse)

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