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 5376 - 5400 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Organism Source
DOID:0080020
  • Jansen's metaphyseal chondrodysplasia
  • Aliases:
    • Jansen Disease
    • Jansen Metaphyseal Dysostosis
    • Jansen metaphyseal chondrodysplasia
    • Murk Jansen Type Metaphyseal Chondrodysplasia
Caenorhabditis elegans
DOID:0111732
  • Eiken syndrome
  • Aliases:
    • Eiken skeletal dysplasia
    • bone modeling defect of hands and feet
Caenorhabditis elegans
DOID:0060387
  • chondrodysplasia Blomstrand type
  • Aliases:
    • Blomstrand lethal chondrodysplasia
Caenorhabditis elegans
DOID:12678
  • hypercalcemia
Caenorhabditis elegans
DOID:0111341
  • primary failure of tooth eruption
  • Aliases:
    • PFE
    • dental noneruption
    • familial posterior openbite malocclusion
    • nonsyndromic primary failure of eruption
    • primary retention of teeth
    • unerupted second primary molar
Caenorhabditis elegans
DOID:0111432
  • essential tremor 5
  • Aliases:
    • ETM5
    • hereditary essential tremor 5
Caenorhabditis elegans
DOID:0070068
  • autosomal dominant intellectual developmental disorder 38
  • Aliases:
    • MRD38
    • PRELDS
    • autosomal dominant mental retardation 38
    • autosomal dominant non-syndromic intellectual disability 38
    • psychomotor retardation, epilepsy, and language disability syndrome
Caenorhabditis elegans
DOID:0080463
  • developmental and epileptic encephalopathy 33
  • Aliases:
    • DEE33
    • early infantile epileptic encephalopathy 33
Caenorhabditis elegans
DOID:2560
  • morphine dependence
Caenorhabditis elegans
DOID:0060001
  • withdrawal disorder
Caenorhabditis elegans
DOID:670
  • amphetamine abuse
Caenorhabditis elegans
DOID:0060307
  • autosomal dominant intellectual developmental disorder
  • Aliases:
    • autosomal dominant mental retardation
    • autosomal dominant non-syndromic mental retardation
Caenorhabditis elegans
DOID:0060823
  • syndromic X-linked intellectual disability 94
  • Aliases:
    • MRX94
    • MRXS29
    • mental retardation, X-linked 94
    • syndromic X-linked intellectual disability due to GRIA3 anomalies
    • syndromic X-linked mental retardation 29
    • syndromic X-linked mental retardation Wu type
Caenorhabditis elegans
DOID:0081235
  • autosomal recessive intellectual developmental disorder 76
Caenorhabditis elegans
DOID:5418
  • schizoaffective disorder
Caenorhabditis elegans
DOID:331
  • central nervous system disease
Caenorhabditis elegans
DOID:4480
  • achondroplasia
  • Aliases:
    • Achondroplastic physique
    • Chondrodystrophia
    • osteosclerosis congenita
Homo sapiens (human)
DOID:0112282
  • spondyloepiphyseal dysplasia Kimberley type
  • Aliases:
    • SEDK
Homo sapiens (human)
DOID:0080240
  • non-syndromic X-linked intellectual disability 106
  • Aliases:
    • MRX106
    • X-linked mental retardation 106
Caenorhabditis elegans
DOID:0080953
  • amelogenesis imperfecta type 1J
  • Aliases:
    • Amelogenesis imperfecta, type IJ
Caenorhabditis elegans
DOID:0080567
  • congenital disorder of glycosylation Ip
  • Aliases:
    • congenital disorder of glycosylation 1p
Caenorhabditis elegans
DOID:0070299
  • multiple epiphyseal dysplasia 5
  • Aliases:
    • BHMED
    • EDM5
    • bilateral hereditary microepiphyseal dysplasia
    • multiple epiphyseal dysplasia MATN3-related
Caenorhabditis elegans
DOID:0080490
  • mucolipidosis type IV
Caenorhabditis elegans
DOID:3343
  • glycoproteinosis
  • Aliases:
    • Mucolipidosis type I
    • sialidosis
Caenorhabditis elegans
DOID:0060450
  • Lisch epithelial corneal dystrophy
  • Aliases:
    • LECD
    • band-shaped and whorled microcystic
Caenorhabditis elegans

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Supported by JST NBDC Grant Number JPMJND2204

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Last updated: December 9, 2024