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 8526 - 8550 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼ Source
DOID:0070469
  • neurodevelopmental disorder with dysmorphic facies and thin corpus callosum
  • Aliases:
    • NEDDFAC
Homo sapiens (human)
DOID:13689
  • prostate calculus
  • Aliases:
    • Prostatic lithiasis
    • Prostatic stone
    • Stone of prostate
    • calculus of prostate
Homo sapiens (human)
DOID:0111406
  • Fraser syndrome 3
  • Aliases:
    • FRASRS3
Homo sapiens (human)
DOID:0111555
  • Alkuraya-Kucinskas syndrome
  • Aliases:
    • ALKKUCS
Homo sapiens (human)
DOID:0111960
  • immunodeficiency 15A
  • Aliases:
    • IMD15A
Homo sapiens (human)
DOID:3535
  • Unverricht-Lundborg syndrome
  • Aliases:
    • Unverricht - Lundborg disease
    • Unverricht's disease
    • Unverricht-Lundborg disease
Homo sapiens (human)
DOID:369
  • olfactory neuroblastoma
  • Aliases:
    • Asthesioneuroblastoma
    • Esthesioneuroblastoma
    • Esthesioneuroepithelioma
    • Olfactory Esthesioneuroblastoma
    • paranasal sinus Olfactory neuroblastoma
Homo sapiens (human)
DOID:0080250
  • erythrokeratodermia variabilis et progressiva 4
Homo sapiens (human)
DOID:635
  • acquired immunodeficiency syndrome
  • Aliases:
    • AIDS
    • acquired Immune deficiency
Homo sapiens (human)
DOID:0111682
  • diffuse cystic renal dysplasia
  • Aliases:
    • CYSRD
    • renal dysplasia diffuse cystic
    • susceptibility to cystic renal dysplasia
Homo sapiens (human)
DOID:10646
  • schizotypal personality disorder
Homo sapiens (human)
DOID:321
  • tropical spastic paraparesis
  • Aliases:
    • HTLV-associated myelopathy
    • Tropical spastic paralysis
    • Tropical spastic paraplegia
Homo sapiens (human)
DOID:0111574
  • autosomal recessive woolly hair 3
  • Aliases:
    • ARWH3
Homo sapiens (human)
DOID:0060867
  • macrocephaly-autism syndrome
  • Aliases:
    • macrocephaly-intellectual disability-autism syndrome
Homo sapiens (human)
DOID:1338
  • congenital dyserythropoietic anemia
  • Aliases:
    • congenital dyshaematopoietic anaemia
Homo sapiens (human)
DOID:10155
  • intestinal cancer
  • Aliases:
    • malignant intestinal tumors
    • malignant neoplasm of intestine
Homo sapiens (human)
DOID:0070114
  • Niemann-Pick disease type C2
  • Aliases:
    • NPC2
Homo sapiens (human)
DOID:11723
  • Duchenne muscular dystrophy
  • Aliases:
    • Muscular dystrophy, Duchenne
Homo sapiens (human)
DOID:891
  • progressive myoclonus epilepsy
  • Aliases:
    • PME
    • progressive myoclonic epilepsy
Homo sapiens (human)
DOID:0060439
  • lysinuric protein intolerance
  • Aliases:
    • LPI
    • dibasic amino aciduria II
    • hyperdibasic aminoaciduria
Homo sapiens (human)
DOID:0112204
  • developmental and epileptic encephalopathy 68
  • Aliases:
    • DEE68
    • early infantile epileptic encephalopathy 68
Homo sapiens (human)
DOID:12638
  • hypertrophic pyloric stenosis
  • Aliases:
    • congenital hypertrophic pyloric stenosis
    • congenital or infantile stricture of pylorus
Homo sapiens (human)
DOID:0070398
  • hypomyelinating leukodystrophy 15
  • Aliases:
    • HLD15
Homo sapiens (human)
DOID:0080807
  • autosomal dominant craniodiaphyseal dysplasia
Homo sapiens (human)
DOID:0070403
  • hypomyelinating leukodystrophy 26
  • Aliases:
    • HLD26
Homo sapiens (human)

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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