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 July 29, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 7726 - 7750 of 7942 in total
Disease ID Disease Name ▼ Gene Symbol Gene ID Organism
DOID:0110169
  • Charcot-Marie-Tooth disease axonal type 2P
  • Aliases:
    • CMT2P
    • Charcot-Marie-Tooth disease type 2P
    • Charcot-Marie-Tooth neuropathy type 2P
Homo sapiens (human)
DOID:0110175
  • Charcot-Marie-Tooth disease axonal type 2O
  • Aliases:
    • Charcot-Marie-Tooth neuropathy axonal type 2O
    • autosomal dominant Charcot-Marie-Tooth disease type 2O
    • autosomal dominant axonal Charcot-Marie-Tooth disease type 2O
Homo sapiens (human)
DOID:0110177
  • Charcot-Marie-Tooth disease axonal type 2N
  • Aliases:
    • CMT2N
    • Charcot-Marie-Tooth neuropathy axonal type 2N
    • autosomal dominant Charcot-Marie-Tooth disease type 2N
    • autosomal dominant axonal Charcot-Marie-Tooth disease type 2N
Homo sapiens (human)
DOID:0110174
  • Charcot-Marie-Tooth disease axonal type 2L
  • Aliases:
    • CMT2L
    • Charcot-Marie-Tooth neuropathy axonal type 2L
    • autosomal dominant Charcot-Marie-Tooth disease type 2L
    • autosomal dominant axonal Charcot-Marie-Tooth disease type 2L
Homo sapiens (human)
DOID:0110167
  • Charcot-Marie-Tooth disease axonal type 2K
  • Aliases:
    • ARCMT2K
    • Charcot-Marie-Tooth neuropathy axonal type 2K
    • autosomal recessive Charcot-Marie-Tooth disease with hoarseness
    • autosomal recessive axonal CMT4C4
    • autosomal recessive axonal Charcot-Marie-Tooth disease disease type 2K
    • autosomal recessive axonal Charcot-Marie-Tooth disease type 2K
Homo sapiens (human)
DOID:0110166
  • Charcot-Marie-Tooth disease axonal type 2H
  • Aliases:
    • AR-CMT2C
    • Autosomal recessive axonal CMT4C2
    • Axonal Charcot-Marie-Tooth disease with pyramidal involvement
    • CMT2H
    • Charcot-Marie-Tooth disease type 2H
    • autosomal recessive axonal Charcot-Marie-Tooth disease with pyramidal features
    • autosomal recessive axonal Charcot-Marie-Tooth neuropathy with pyramidal features
Homo sapiens (human)
DOID:0110163
  • Charcot-Marie-Tooth disease axonal type 2F
  • Aliases:
    • CMT2F
    • Charcot-Marie-Tooth neuronal type 2F
    • Charcot-Marie-Tooth neuropathy type 2F
    • autosomal dominant Charcot-Marie-Tooth disease type 2F
Homo sapiens (human)
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
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
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
Homo sapiens (human)
DOID:0110211
  • Charcot-Marie-Tooth disease X-linked recessive 3
  • Aliases:
    • CMT3X
    • CMTX3
    • Charcot-Marie-Tooth neuropathy X-linked recessive 3
    • X-linked Charcot-Marie-Tooth disease type 3
Homo sapiens (human)
DOID:0110208
  • Charcot-Marie-Tooth disease X-linked recessive 2
  • Aliases:
    • CMTX2
    • Charcot-Marie-Tooth neuropathy X-linked recessive 2
    • X-linked Charcot-Marie-Tooth disease type 2
Homo sapiens (human)
DOID:0110207
  • Charcot-Marie-Tooth disease X-linked dominant 6
  • Aliases:
    • CMT6X
    • CMTX6
    • Charcot-Marie-Tooth neuropathy X-linked dominant 6
    • X-linked Charcot-Marie-Tooth disease type 6
Homo sapiens (human)
DOID:0110209
  • Charcot-Marie-Tooth disease X-linked dominant 1
  • Aliases:
    • CMT1X
    • CMTX1
    • Charcot-Marie-Tooth neuropathy X-linked dominant 1
    • X-linked Charcot-Marie-Tooth disease type 1
Homo sapiens (human)
DOID:0060563
  • Char syndrome
Mus musculus (house mouse)
DOID:0060563
  • Char syndrome
Homo sapiens (human)
DOID:11554
  • Chandler syndrome
  • Aliases:
    • Chandler's syndrome
    • Dystrophy of corneal endothelium
    • Endothelial corneal dystrophy
    • Posterior membrane corneal dystrophy
Homo sapiens (human)
DOID:0050729
  • Chanarin-Dorfman syndrome
  • Aliases:
    • neutral lipid storage disease
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
Homo sapiens (human)
DOID:0090015
  • Cenani-Lenz syndactyly syndrome
  • Aliases:
    • syndactyly type 7
Homo sapiens (human)
DOID:11577
  • Cauda equina syndrome
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:0111157
  • Castleman disease
  • Aliases:
    • angiofollicular lymph hyperplasia
    • angiofollicular lymph node hyperplasia
    • giant lymph node hyperplasia
    • lymphoid hamartoma
Homo sapiens (human)
DOID:0050876
  • Caroli disease
Homo sapiens (human)
DOID:0080533
  • Carney-Stratakis syndrome
Homo sapiens (human)

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Last updated: August 19, 2024