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 15376 - 15400 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:0050814
  • temtamy preaxial brachydactyly syndrome
  • Aliases:
    • PREAXIAL BRACHYDACTYLY SYNDROME, TEMTAMY TYPE
Rattus norvegicus (Norway rat)
DOID:6132
  • bronchitis
  • Aliases:
    • CI - Chest infection
    • Chest infection
    • acute Bronchitis
    • chest cold
    • chronic bronchitis
    • recurrent wheezy bronchitis
Homo sapiens (human)
DOID:0111206
  • autosomal dominant distal hereditary motor neuronopathy 2
  • Aliases:
    • HMN II
    • HMN IIA
    • HMN2
    • HMN2A
    • autosomal dominant adult spinal muscular atrophy IIA
    • distal hereditary motor neuronopathy type 2
    • distal hereditary motor neuronopathy type 2A
    • distal hereditary motor neuropathy type II
    • distal hereditary motor neuropathy type IIA
    • spinal Charcot-Marie-Tooth disease IIA
Homo sapiens (human)
DOID:0080489
  • GM1 gangliosidosis type 3
  • Aliases:
    • adult-onset GM1 gangliosidosis
Mus musculus (house mouse)
DOID:0111061
  • familial hypobetalipoproteinemia 2
  • Aliases:
    • FHBL2
    • combined familial hypolipidemia
Rattus norvegicus (Norway rat)
DOID:11714
  • gestational diabetes
  • Aliases:
    • GDM
    • Gestational diabetes mellitus
    • Maternal gestational diabetes mellitus
Rattus norvegicus (Norway rat)
DOID:11823
  • hepatorenal syndrome
Mus musculus (house mouse)
DOID:8692
  • myeloid leukemia
  • Aliases:
    • Non-Lymphocytic Leukemia
    • leukaemia myelogenous
    • leukemia myelogenous
    • myeloid granulocytic leukaemia
    • myeloid granulocytic leukemia
    • myeloid leukaemia
Saccharomyces cerevisiae S288C
DOID:0060774
  • congenital diarrhea
Homo sapiens (human)
DOID:0081120
  • Graves ophthalmopathy
  • Aliases:
    • Graves orbitopathy
    • Thyroid associated ophthalmopathy
    • thyroid eye disease
Homo sapiens (human)
DOID:0112122
  • X-linked epilepsy with variable learning disabilities and behavior disorders
  • Aliases:
    • X-linked epilepsy-learning disabilities-behavior disorders syndrome
Drosophila melanogaster (fruit fly)
DOID:0070114
  • Niemann-Pick disease type C2
  • Aliases:
    • NPC2
Mus musculus (house mouse)
DOID:0111729
  • familial episodic pain syndrome 1
  • Aliases:
    • FEPS1
Drosophila melanogaster (fruit fly)
DOID:2696
  • Leydig cell tumor
  • Aliases:
    • Leydig cell neoplasm
Rattus norvegicus (Norway rat)
DOID:0111007
  • X-linked cone-rod dystrophy 3
  • Aliases:
    • CORDX3
Danio rerio (zebrafish)
DOID:12176
  • goiter
  • Aliases:
    • goitre
Mus musculus (house mouse)
DOID:0060399
  • chromosome 16p12.1 deletion syndrome
Mus musculus (house mouse)
DOID:0050718
  • vitamin metabolic disorder
Danio rerio (zebrafish)
DOID:10762
  • portal hypertension
Mus musculus (house mouse)
DOID:0111636
  • autosomal recessive nonsyndromic deafness 113
  • Aliases:
    • DFNB113
    • autosomal recessive deafness 113
Homo sapiens (human)
DOID:0090080
  • hypogonadotropic hypogonadism 16 with or without anosmia
Rattus norvegicus (Norway rat)
DOID:0080176
  • meningococcal meningitis
Rattus norvegicus (Norway rat)
DOID:1307
  • dementia
Drosophila melanogaster (fruit fly)
DOID:1577
  • limited scleroderma
  • Aliases:
    • Limited cutaneous systemic sclerosis
    • systemic sclerosis, limited
Caenorhabditis elegans
DOID:0081210
  • autosomal recessive intellectual developmental disorder 46
Mus musculus (house mouse)

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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