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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 3626 - 3650 of 4649 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source ▼
DOID:0080066
  • autosomal recessive spinocerebellar ataxia 20
  • Aliases:
    • SCAR20
Homo sapiens (human)
DOID:0080065
  • autosomal recessive spinocerebellar ataxia 19
  • Aliases:
    • Lichtenstein-Knorr syndrome
    • SCAR19
Homo sapiens (human)
DOID:0080062
  • autosomal recessive spinocerebellar ataxia 13
  • Aliases:
    • SCAR13
Homo sapiens (human)
DOID:0080061
  • autosomal recessive spinocerebellar ataxia 2
  • Aliases:
    • SCAR2
Homo sapiens (human)
DOID:0080059
  • autosomal recessive spinocerebellar ataxia 7
  • Aliases:
    • SCAR7
Homo sapiens (human)
DOID:0080058
  • autosomal recessive spinocerebellar ataxia 14
  • Aliases:
    • SCAR14
Homo sapiens (human)
DOID:0080056
  • achondrogenesis type II
Homo sapiens (human)
DOID:0080054
  • achondrogenesis type IA
  • Aliases:
    • achondrogenesis Houston-Harris type
Homo sapiens (human)
DOID:0080053
  • Albright's hereditary osteodystrophy
  • Aliases:
    • Albright hereditary osteodystrophy
    • pseudohypoparathyroidism type 1a
Homo sapiens (human)
DOID:0080052
  • acromesomelic dysplasia, Grebe type
  • Aliases:
    • acromesomelic dysplasia-2A
    • grebe chondrodysplasia
Homo sapiens (human)
DOID:0080051
  • acromesomelic dysplasia, Hunter-Thompson type
  • Aliases:
    • acromesomelic dwarfism
    • acromesomelic dysplasia-2C
Homo sapiens (human)
DOID:0080050
  • acromesomelic dysplasia, Maroteaux type
  • Aliases:
    • acromesomelic dysplasia-1
Homo sapiens (human)
DOID:0080047
  • pseudoachondroplasia
  • Aliases:
    • SPONDYLOEPIPHYSEAL DYSPLASIA, PSEUDOACHONDROPLASTIC
    • pseudoachondroplastic dysplasia
Homo sapiens (human)
DOID:0080046
  • Stickler syndrome
Homo sapiens (human)
DOID:0080045
  • Kniest dysplasia
Homo sapiens (human)
DOID:0080044
  • hypochondrogenesis
Homo sapiens (human)
DOID:0080042
  • autosomal recessive spinocerebellar ataxia 18
  • Aliases:
    • SCAR18
Homo sapiens (human)
DOID:0080041
  • hypochondroplasia
Homo sapiens (human)
DOID:0080038
  • pycnodysostosis
Homo sapiens (human)
DOID:0080037
  • Worth syndrome
  • Aliases:
    • Worth's syndrome
    • autosomal dominant endosteal hyperostosis
    • autosomal dominant osteosclerosis
    • benign form of Worth hyperostosis corticalis generalisata with torus platinus
Homo sapiens (human)
DOID:0080036
  • SOST-related sclerosing bone dysplasia
  • Aliases:
    • van Buchem disease
Homo sapiens (human)
DOID:0080030
  • spondyloepimetaphyseal dysplasia, Missouri type
Homo sapiens (human)
DOID:0080028
  • spondyloepimetaphyseal dysplasia, Strudwick type
Homo sapiens (human)
DOID:0080027
  • spondyloepimetaphyseal dysplasia
Homo sapiens (human)
DOID:0080026
  • otospondylomegaepiphyseal dysplasia, autosomal recessive
  • Aliases:
    • CHONDRODYSTROPHY WITH SENSORINEURAL DEAFNESS
    • NANCE-INSLEY SYNDROME
    • NANCE-SWEENEY CHONDRODYSPLASIA
    • OSMEDB
Homo sapiens (human)
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Acknowledgements

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