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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 5426 - 5450 of 15957 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Organism Source
DOID:0050338
  • primary bacterial infectious disease
Drosophila melanogaster (fruit fly)
DOID:0112189
  • thyroid dyshormonogenesis 6
  • Aliases:
    • TDH6
    • genetic defect in thyroid hormonogenesis 6
Drosophila melanogaster (fruit fly)
DOID:1498
  • cholera
  • Aliases:
    • Cholera - Vibrio cholerae
    • Cholera due to Vibrio cholerae
    • Vibrio cholerae
Drosophila melanogaster (fruit fly)
DOID:0050338
  • primary bacterial infectious disease
Rattus norvegicus (Norway rat)
DOID:0050328
  • congenital hypothyroidism
Mus musculus (house mouse)
DOID:0050338
  • primary bacterial infectious disease
Mus musculus (house mouse)
DOID:9281
  • phenylketonuria
  • Aliases:
    • Folling's disease
    • PKU
    • maternal phenylketonuria
    • phenylalaninemia
Rattus norvegicus (Norway rat)
DOID:1498
  • cholera
  • Aliases:
    • Cholera - Vibrio cholerae
    • Cholera due to Vibrio cholerae
    • Vibrio cholerae
Rattus norvegicus (Norway rat)
DOID:0112189
  • thyroid dyshormonogenesis 6
  • Aliases:
    • TDH6
    • genetic defect in thyroid hormonogenesis 6
Rattus norvegicus (Norway rat)
DOID:0112184
  • thyroid dyshormonogenesis 5
  • Aliases:
    • TDH5
    • genetic defect in thyroid hormonogenesis 5
Mus musculus (house mouse)
DOID:0060765
  • autosomal dominant Robinow syndrome 2
  • Aliases:
    • DRS2
Mus musculus (house mouse)
DOID:0070351
  • spinal muscular atrophy with lower extremity predominant 1
  • Aliases:
    • spinal muscular atrophy with lower extremity predominance 1
Mus musculus (house mouse)
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
Mus musculus (house mouse)
DOID:0070043
  • autosomal dominant intellectual developmental disorder 13
  • Aliases:
    • MRD13
    • autosomal dominant mental retardation 13
    • autosomal dominant non-syndromic intellectual disability 13
    • mental retardation, autosomal dominant 13, with neuronal migration defects
Mus musculus (house mouse)
DOID:0050557
  • congenital muscular dystrophy
Rattus norvegicus (Norway rat)
DOID:0070043
  • autosomal dominant intellectual developmental disorder 13
  • Aliases:
    • MRD13
    • autosomal dominant mental retardation 13
    • autosomal dominant non-syndromic intellectual disability 13
    • mental retardation, autosomal dominant 13, with neuronal migration defects
Rattus norvegicus (Norway rat)
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
Rattus norvegicus (Norway rat)
DOID:0070351
  • spinal muscular atrophy with lower extremity predominant 1
  • Aliases:
    • spinal muscular atrophy with lower extremity predominance 1
Rattus norvegicus (Norway rat)
DOID:14679
  • VACTERL association
Mus musculus (house mouse)
DOID:0110087
  • asphyxiating thoracic dystrophy 3
  • Aliases:
    • ATD3
    • SRPS1
    • SRPS2B
    • SRPS3
    • SRTD3
    • Saldino-Noonan syndrome
    • Verma-Naumoff syndrome
    • polydactyly with neonatal chondrodystrophy, type I
    • polydactyly with neonatal chondrodystrophy, type III
    • short rib-polydactyly syndrome, type I
    • short rib-polydactyly syndrome, type IIB
    • short-rib thoracic dysplasia 3 with or without polydactyly
Mus musculus (house mouse)
DOID:0060612
  • abdominal obesity-metabolic syndrome 3
Mus musculus (house mouse)
DOID:11724
  • limb-girdle muscular dystrophy
  • Aliases:
    • Erb's muscular dystrophy
    • Leyden-Mbius muscular dystrophy
    • limb girdle muscular dystrophy
Mus musculus (house mouse)
DOID:11720
  • distal myopathy
  • Aliases:
    • distal muscular dystrophy
Mus musculus (house mouse)
DOID:0111187
  • distal myopathy with anterior tibial onset
  • Aliases:
    • DMAT
    • distal muscular dystrophy with anterior tibial onset
Mus musculus (house mouse)
DOID:0110276
  • autosomal recessive limb-girdle muscular dystrophy type 2B
  • Aliases:
    • LGMD2B
    • LGMD3
    • limb-girdle muscular dystrophy due to dysferlin deficiency
    • limb-girdle muscular dystrophy type 3
Mus musculus (house mouse)
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Supported by JST NBDC Grant Number JPMJND2204

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Last updated: December 9, 2024