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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 7676 - 7700 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source ▲
DOID:0111594
  • distal arthrogryposis type 5D
  • Aliases:
    • DA5D
    • distal arthrogryposis type 5 without ophthalmoparesis
    • distal arthrogryposis type 5 without ophthalmoplegia
Mus musculus (house mouse)
DOID:0111594
  • distal arthrogryposis type 5D
  • Aliases:
    • DA5D
    • distal arthrogryposis type 5 without ophthalmoparesis
    • distal arthrogryposis type 5 without ophthalmoplegia
Rattus norvegicus (Norway rat)
DOID:0111595
  • congenital contractural arachnodactyly
  • Aliases:
    • Beals syndrome
    • Beals-Hecht syndrome
    • CCA
    • arachnodactyly, contractural Beals type
    • contractures, multiple with arachnodactyly
    • distal arthrogryposis type 9
    • ear anomalies-contractures-dysplasia of bone with kyphoscoliosis
Caenorhabditis elegans
DOID:0111595
  • congenital contractural arachnodactyly
  • Aliases:
    • Beals syndrome
    • Beals-Hecht syndrome
    • CCA
    • arachnodactyly, contractural Beals type
    • contractures, multiple with arachnodactyly
    • distal arthrogryposis type 9
    • ear anomalies-contractures-dysplasia of bone with kyphoscoliosis
Homo sapiens (human)
DOID:0111595
  • congenital contractural arachnodactyly
  • Aliases:
    • Beals syndrome
    • Beals-Hecht syndrome
    • CCA
    • arachnodactyly, contractural Beals type
    • contractures, multiple with arachnodactyly
    • distal arthrogryposis type 9
    • ear anomalies-contractures-dysplasia of bone with kyphoscoliosis
Mus musculus (house mouse)
DOID:0111596
  • distal arthrogryposis type 1
  • Aliases:
    • DA1
    • digitotalar dysmorphism
Homo sapiens (human)
DOID:0111596
  • distal arthrogryposis type 1
  • Aliases:
    • DA1
    • digitotalar dysmorphism
Mus musculus (house mouse)
DOID:0111598
  • distal arthrogryposis type 1B
  • Aliases:
    • DA1B
Homo sapiens (human)
DOID:0111599
  • distal arthrogryposis type 2B
  • Aliases:
    • DA2B
    • Freeman-Sheldon syndrome variant
    • Sheldon-Hall syndrome
Mus musculus (house mouse)
DOID:0111602
  • distal arthrogryposis type 2B3
  • Aliases:
    • DA2B3
    • distal arthrogryposis type 2B3 (Sheldon-Hall)
Homo sapiens (human)
DOID:0111602
  • distal arthrogryposis type 2B3
  • Aliases:
    • DA2B3
    • distal arthrogryposis type 2B3 (Sheldon-Hall)
Mus musculus (house mouse)
DOID:0111605
  • distal arthrogryposis type 2A
  • Aliases:
    • DA2A
    • distal arthrogryposis type 2A (Freeman-Sheldon)
Mus musculus (house mouse)
DOID:0111605
  • distal arthrogryposis type 2A
  • Aliases:
    • DA2A
    • distal arthrogryposis type 2A (Freeman-Sheldon)
Homo sapiens (human)
DOID:0111607
  • distal arthrogryposis type 3
  • Aliases:
    • DA3
    • Gordon syndrome
    • camptodactyly-cleft palate-clubfoot syndrome
    • distal arthrogryposis multiplex congenita type IIA
Homo sapiens (human)
DOID:0111607
  • distal arthrogryposis type 3
  • Aliases:
    • DA3
    • Gordon syndrome
    • camptodactyly-cleft palate-clubfoot syndrome
    • distal arthrogryposis multiplex congenita type IIA
Mus musculus (house mouse)
DOID:0111607
  • distal arthrogryposis type 3
  • Aliases:
    • DA3
    • Gordon syndrome
    • camptodactyly-cleft palate-clubfoot syndrome
    • distal arthrogryposis multiplex congenita type IIA
Caenorhabditis elegans
DOID:0111608
  • distal arthrogryposis type 5
  • Aliases:
    • DA5
    • DAIIB
    • arthrogryposis-oculomotor limitation-electroretinal anomalies syndrome
    • distal arthrogryposis type IIB
    • distal arthrogryposis with ophthalmoplegia
    • oculomelic amyoplasia
Homo sapiens (human)
DOID:0111608
  • distal arthrogryposis type 5
  • Aliases:
    • DA5
    • DAIIB
    • arthrogryposis-oculomotor limitation-electroretinal anomalies syndrome
    • distal arthrogryposis type IIB
    • distal arthrogryposis with ophthalmoplegia
    • oculomelic amyoplasia
Caenorhabditis elegans
DOID:0111608
  • distal arthrogryposis type 5
  • Aliases:
    • DA5
    • DAIIB
    • arthrogryposis-oculomotor limitation-electroretinal anomalies syndrome
    • distal arthrogryposis type IIB
    • distal arthrogryposis with ophthalmoplegia
    • oculomelic amyoplasia
Mus musculus (house mouse)
DOID:0111611
  • autosomal recessive spinocerebellar ataxia 4
  • Aliases:
    • SCA24
    • SCAR4
    • SCASI
    • autosomal recessive cerebellar ataxia-saccadic intrusion syndrome
    • spinocerebellar ataxia 24
    • spinocerebellar ataxia with saccadic intrusions
Mus musculus (house mouse)
DOID:0111611
  • autosomal recessive spinocerebellar ataxia 4
  • Aliases:
    • SCA24
    • SCAR4
    • SCASI
    • autosomal recessive cerebellar ataxia-saccadic intrusion syndrome
    • spinocerebellar ataxia 24
    • spinocerebellar ataxia with saccadic intrusions
Homo sapiens (human)
DOID:0111614
  • autosomal recessive spinocerebellar ataxia 22
  • Aliases:
    • SCAR22
Homo sapiens (human)
DOID:0111618
  • autosomal recessive spinocerebellar ataxia 8
  • Aliases:
    • ARCA1
    • Autosomal recessive cerebellar ataxia type 1
    • SCAR8
    • SYNE1-related autosomal recessive cerebellar ataxia
    • autosomal recessive ataxia, Beauce type
    • recessive ataxia of Beauce
Drosophila melanogaster (fruit fly)
DOID:0111618
  • autosomal recessive spinocerebellar ataxia 8
  • Aliases:
    • ARCA1
    • Autosomal recessive cerebellar ataxia type 1
    • SCAR8
    • SYNE1-related autosomal recessive cerebellar ataxia
    • autosomal recessive ataxia, Beauce type
    • recessive ataxia of Beauce
Homo sapiens (human)
DOID:0111618
  • autosomal recessive spinocerebellar ataxia 8
  • Aliases:
    • ARCA1
    • Autosomal recessive cerebellar ataxia type 1
    • SCAR8
    • SYNE1-related autosomal recessive cerebellar ataxia
    • autosomal recessive ataxia, Beauce type
    • recessive ataxia of Beauce
Mus musculus (house mouse)
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Last updated: August 19, 2024