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 1351 - 1375 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼ Source
DOID:0050758
  • metabolic acidosis
Saccharomyces cerevisiae S288C
DOID:0111862
  • congenital bilateral absence of vas deferens
  • Aliases:
    • CAVD
    • CBAVD
    • congenital bilateral agenesis of vas deferens
    • congenital bilateral aplasia of vas deferens
Saccharomyces cerevisiae S288C
DOID:11088
  • asphyxia neonatorum
  • Aliases:
    • Asphyxia - birth
    • Asphyxia, in liveborn infant
    • Birth asphyxia
    • postnatal asphyxia
Saccharomyces cerevisiae S288C
DOID:0090057
  • X-linked dystonia-parkinsonism
Saccharomyces cerevisiae S288C
DOID:1024
  • leprosy
Saccharomyces cerevisiae S288C
DOID:678
  • progressive supranuclear palsy
  • Aliases:
    • Steele-Richardson-Olszewski syndrome
    • progressive supranuclear ophthalmoplegia
Saccharomyces cerevisiae S288C
DOID:4006
  • bladder urothelial carcinoma
  • Aliases:
    • bladder transitional cell carcinoma
    • transitional cell carcinoma of bladder
    • urinary bladder urothelial carcinoma
    • urothelial bladder carcinoma
Saccharomyces cerevisiae S288C
DOID:0060807
  • syndromic X-linked intellectual disability Najm type
  • Aliases:
    • MICPCH
    • X-linked intellectual disability-microcephaly-pontocerebellar hypoplasia syndrome
    • mental retardation and microcephaly with pontine and cerebellar hypoplasia
Saccharomyces cerevisiae S288C
DOID:0110861
  • autosomal recessive polycystic kidney disease
  • Aliases:
    • Arpkd
    • Pkhd1
    • Polycystic Kidney Disease, Infantile, Type I
    • Polycystic Kidney and Hepatic Disease 1
Saccharomyces cerevisiae S288C
DOID:0050127
  • sinusitis
Saccharomyces cerevisiae S288C
DOID:1574
  • alcohol use disorder
  • Aliases:
    • Ethanol abuse
    • alcohol abuse
Saccharomyces cerevisiae S288C
DOID:83
  • cataract
Saccharomyces cerevisiae S288C
DOID:0060309
  • syndromic X-linked intellectual disability
  • Aliases:
    • syndromic X-linked mental retardation
Saccharomyces cerevisiae S288C
DOID:2747
  • glycogen storage disease
  • Aliases:
    • glycogenosis
Saccharomyces cerevisiae S288C
DOID:0111308
  • familial febrile seizures 11
  • Aliases:
    • FEB11
    • familial febrile convulsions 11
Saccharomyces cerevisiae S288C
DOID:4450
  • renal cell carcinoma
  • Aliases:
    • RCC
    • adenocarcinoma of kidney
    • hypernephroma
Saccharomyces cerevisiae S288C
DOID:13258
  • typhoid fever
  • Aliases:
    • Typhoid
Saccharomyces cerevisiae S288C
DOID:0081098
  • autosomal recessive intellectual developmental disorder 13
Saccharomyces cerevisiae S288C
DOID:1287
  • cardiovascular system disease
  • Aliases:
    • disease of subdivision of hemolymphoid system
Saccharomyces cerevisiae S288C
DOID:2352
  • hemochromatosis
  • Aliases:
    • Haemochromatosis
    • diabetes bronze
    • iron storage disorder
Saccharomyces cerevisiae S288C
DOID:0080573
  • congenital disorder of glycosylation Ix
  • Aliases:
    • congenital disorder of glycosylation 1x
Saccharomyces cerevisiae S288C
DOID:7004
  • ACTH-secreting pituitary adenoma
  • Aliases:
    • ACTH-Producing Pituitary Adenoma
    • Corticotroph adenoma
    • Corticotropinoma
Saccharomyces cerevisiae S288C
DOID:332
  • amyotrophic lateral sclerosis
  • Aliases:
    • ALS
    • Lou Gehrig's disease
    • motor neuron disease, bulbar
Saccharomyces cerevisiae S288C
DOID:5082
  • liver cirrhosis
  • Aliases:
    • Cirrhosis
    • cirrhosis of liver
Saccharomyces cerevisiae S288C
DOID:2476
  • hereditary spastic paraplegia
  • Aliases:
    • French settlement disease
    • Strumpell-Lorrain disease
    • familial spastic paraplegia
    • hereditary spastic paraparesis
Saccharomyces cerevisiae S288C

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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