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 15526 - 15550 of 15957 in total
Disease ID Disease Name ▼ Gene Symbol Gene ID Organism Source
DOID:0110180
  • Charcot-Marie-Tooth disease axonal type 2CC
  • Aliases:
    • CMT2CC
    • Charcot-Marie-Tooth neuropathy type 2CC
Mus musculus (house mouse)
DOID:0110182
  • Charcot-Marie-Tooth disease axonal type 2C
  • Aliases:
    • CMT2C
    • Charcot-Marie-Tooth neuropathy type 2C
    • HMSN2C
    • autosomal cominant axonal Charcot-Marie-Tooth disease type 2C
    • autosomal dominant Charcot-Marie-Tooth disease type 2C
    • hereditary motor and sensory neuropathy type IIc
Mus musculus (house mouse)
DOID:0110210
  • Charcot-Marie-Tooth disease X-linked recessive 5
  • Aliases:
    • CMT5X
    • CMTX5
    • Charcot-Marie-Tooth neuropathy X-linked recessive 5
    • Rosenberg-Chutorian syndrome
    • X-linked Charcot-Marie-Tooth disease type 5
    • optic atrophy, polyneuropathy, and deafness
Homo sapiens (human)
DOID:0110210
  • Charcot-Marie-Tooth disease X-linked recessive 5
  • Aliases:
    • CMT5X
    • CMTX5
    • Charcot-Marie-Tooth neuropathy X-linked recessive 5
    • Rosenberg-Chutorian syndrome
    • X-linked Charcot-Marie-Tooth disease type 5
    • optic atrophy, polyneuropathy, and deafness
Mus musculus (house mouse)
DOID:0110212
  • Charcot-Marie-Tooth disease X-linked recessive 4
  • Aliases:
    • CMT4X
    • CMTX4
    • Charcot-Marie-Tooth disease with deafness and mental retardation
    • Cowchock syndrome
    • NADMR
    • NAMSD
    • X-linked Charcot-Marie-Tooth disease type 4
    • axonal motor sensory neuropathy with deafness and mental retardation
Homo sapiens (human)
DOID:0110212
  • Charcot-Marie-Tooth disease X-linked recessive 4
  • Aliases:
    • CMT4X
    • CMTX4
    • Charcot-Marie-Tooth disease with deafness and mental retardation
    • Cowchock syndrome
    • NADMR
    • NAMSD
    • X-linked Charcot-Marie-Tooth disease type 4
    • axonal motor sensory neuropathy with deafness and mental retardation
Mus musculus (house mouse)
DOID:0060563
  • Char syndrome
Mus musculus (house mouse)
DOID:0060563
  • Char syndrome
Homo sapiens (human)
DOID:0050729
  • Chanarin-Dorfman syndrome
  • Aliases:
    • neutral lipid storage disease
Rattus norvegicus (Norway rat)
DOID:0050729
  • Chanarin-Dorfman syndrome
  • Aliases:
    • neutral lipid storage disease
Homo sapiens (human)
DOID:0050729
  • Chanarin-Dorfman syndrome
  • Aliases:
    • neutral lipid storage disease
Mus musculus (house mouse)
DOID:12140
  • Chagas disease
  • Aliases:
    • Chagas' disease
    • chagas' disease with digestive system involvement
    • chagas' disease with nervous system involvement
    • chagas' disease with other organ involvement
Mus musculus (house mouse)
DOID:12140
  • Chagas disease
  • Aliases:
    • Chagas' disease
    • chagas' disease with digestive system involvement
    • chagas' disease with nervous system involvement
    • chagas' disease with other organ involvement
Homo sapiens (human)
DOID:12140
  • Chagas disease
  • Aliases:
    • Chagas' disease
    • chagas' disease with digestive system involvement
    • chagas' disease with nervous system involvement
    • chagas' disease with other organ involvement
Caenorhabditis elegans
DOID:12140
  • Chagas disease
  • Aliases:
    • Chagas' disease
    • chagas' disease with digestive system involvement
    • chagas' disease with nervous system involvement
    • chagas' disease with other organ involvement
Rattus norvegicus (Norway rat)
DOID:12140
  • Chagas disease
  • Aliases:
    • Chagas' disease
    • chagas' disease with digestive system involvement
    • chagas' disease with nervous system involvement
    • chagas' disease with other organ involvement
Drosophila melanogaster (fruit fly)
DOID:0090015
  • Cenani-Lenz syndactyly syndrome
  • Aliases:
    • syndactyly type 7
Mus musculus (house mouse)
DOID:0090015
  • Cenani-Lenz syndactyly syndrome
  • Aliases:
    • syndactyly type 7
Homo sapiens (human)
DOID:0081122
  • Catel Manzke syndrome
  • Aliases:
    • Hyperphalangy-clinodactyly of index finger with Pierre Robin syndrome
    • Micrognathia digital syndrome
Homo sapiens (human)
DOID:0090128
  • Carvajal syndrome
  • Aliases:
    • DCWHK
    • dilated cardiomyopathy with woolly hair and keratoderma
    • palmoplantar keratoderma with left ventricular cardiomyopathy and woolly hair
Homo sapiens (human)
DOID:0060234
  • Carpenter syndrome
  • Aliases:
    • acrocephalopolysyndactyly type II
Mus musculus (house mouse)
DOID:0060234
  • Carpenter syndrome
  • Aliases:
    • acrocephalopolysyndactyly type II
Homo sapiens (human)
DOID:0081394
  • Caroli syndrome
Homo sapiens (human)
DOID:0081394
  • Caroli syndrome
Mus musculus (house mouse)
DOID:0050876
  • Caroli disease
Mus musculus (house mouse)

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Last updated: December 9, 2024