Table Filtering
Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
LM-GlycoRepo
Repository for lectin-assisted multimodality data
Resources Genes Glycoproteins Lectins Glycolipids Glycans Pathways Diseases Organisms
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Other Information
Release Statistics Download
Tools
SugarDrawer GlycanBuilder Glycan Converters GlycoMaple GlycomeAtlas LM-GlycomeAtlas GALAXY MCAW GlycoSim GRable
Search Tools
Cross Search Glycan Search Publication Search Programmatic Access
Standards Ontologies Notations
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 11226 - 11250 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source ▼
DOID:0081097
  • Rafiq syndrome
  • Aliases:
    • MENTAL RETARDATION, AUTOSOMAL RECESSIVE 15
Drosophila melanogaster (fruit fly)
DOID:0081097
  • Rafiq syndrome
  • Aliases:
    • MENTAL RETARDATION, AUTOSOMAL RECESSIVE 15
Mus musculus (house mouse)
DOID:0081097
  • Rafiq syndrome
  • Aliases:
    • MENTAL RETARDATION, AUTOSOMAL RECESSIVE 15
Caenorhabditis elegans
DOID:0081097
  • Rafiq syndrome
  • Aliases:
    • MENTAL RETARDATION, AUTOSOMAL RECESSIVE 15
Saccharomyces cerevisiae S288C
DOID:0081097
  • Rafiq syndrome
  • Aliases:
    • MENTAL RETARDATION, AUTOSOMAL RECESSIVE 15
Rattus norvegicus (Norway rat)
DOID:0081082
  • acute myelomonocytic leukemia
Caenorhabditis elegans
DOID:0081082
  • acute myelomonocytic leukemia
Homo sapiens (human)
DOID:0081082
  • acute myelomonocytic leukemia
Mus musculus (house mouse)
DOID:0081075
  • Marsili syndrome
  • Aliases:
    • congenital analgesia
    • congenital insensitivity to pain
Homo sapiens (human)
DOID:0081075
  • Marsili syndrome
  • Aliases:
    • congenital analgesia
    • congenital insensitivity to pain
Mus musculus (house mouse)
DOID:0081074
  • Teebi hypertelorism syndrome 2
Homo sapiens (human)
DOID:0081074
  • Teebi hypertelorism syndrome 2
Rattus norvegicus (Norway rat)
DOID:0081074
  • Teebi hypertelorism syndrome 2
Mus musculus (house mouse)
DOID:0081072
  • craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome
  • Aliases:
    • Cerebro-facio-thoracic dysplasia
    • Cerebrofaciothoracic dysplasia
    • Pascual-Castroviejo syndrome
    • TMCO1 defect syndrome
Homo sapiens (human)
DOID:0081063
  • DICER1 syndrome
  • Aliases:
    • PPB familial tumor susceptibility syndrome
    • Pleuro-pulmonary blastoma familial tumor susceptibility
    • Pleuro-pulmonary blastoma familial tumor susceptibility syndrome
    • Pleuropulmonary blastoma familial tumor susceptibility syndrome
Homo sapiens (human)
DOID:0081061
  • nephrogenic diabetes insipidus type 2
  • Aliases:
    • autosomal nephrogenic diabetes insipidus-2
Homo sapiens (human)
DOID:0081061
  • nephrogenic diabetes insipidus type 2
  • Aliases:
    • autosomal nephrogenic diabetes insipidus-2
Rattus norvegicus (Norway rat)
DOID:0081061
  • nephrogenic diabetes insipidus type 2
  • Aliases:
    • autosomal nephrogenic diabetes insipidus-2
Mus musculus (house mouse)
DOID:0081060
  • X-linked nephrogenic diabetes insipidus
  • Aliases:
    • nephrogenic diabetes insipidus type 1
Mus musculus (house mouse)
DOID:0081060
  • X-linked nephrogenic diabetes insipidus
  • Aliases:
    • nephrogenic diabetes insipidus type 1
Rattus norvegicus (Norway rat)
DOID:0081060
  • X-linked nephrogenic diabetes insipidus
  • Aliases:
    • nephrogenic diabetes insipidus type 1
Caenorhabditis elegans
DOID:0081060
  • X-linked nephrogenic diabetes insipidus
  • Aliases:
    • nephrogenic diabetes insipidus type 1
Homo sapiens (human)
DOID:0081051
  • microcephaly, growth deficiency, seizures, and brain malformations
Mus musculus (house mouse)
DOID:0081048
  • congenital limbs-face contractures-hypotonia-developmental delay syndrome
  • Aliases:
    • CLIFAHDD syndrome
    • congenital contractures of the limbs and face, hypotonia, and developmental delay
Homo sapiens (human)
DOID:0081048
  • congenital limbs-face contractures-hypotonia-developmental delay syndrome
  • Aliases:
    • CLIFAHDD syndrome
    • congenital contractures of the limbs and face, hypotonia, and developmental delay
Mus musculus (house mouse)
Download data in CSV format Download data in TSV format Download data in JSON format
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