GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB), DisGeNET, and Alliance of Genome Resources is integrated into one list.

Source Last Updated
Alliance of Genome Resources July 29, 2024
DisGeNET July 29, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 2026 - 2050 of 4621 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism
DOID:6536
  • plasma cell neoplasm
  • Aliases:
    • Plasma cell dyscrasia
    • Plasma cell tumour
    • Plasmacytic tumor
Homo sapiens (human)
DOID:0080147
  • lymphoblastic lymphoma
Homo sapiens (human)
DOID:3149
  • keratoacanthoma
Homo sapiens (human)
DOID:0112198
  • spondyloepimetaphyseal dysplasia with joint laxity type 1
  • Aliases:
    • SEMDJL1
    • spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures
Homo sapiens (human)
DOID:0111148
  • isolated ectopia lentis
  • Aliases:
    • IEL
    • familial ectopia lentis
Homo sapiens (human)
DOID:0050802
  • Ehlers-Danlos syndrome spondylodysplastic type 2
  • Aliases:
    • EHLERS-DANLOS SYNDROME, PROGEROID TYPE, 2
    • Ehlers-Danlos syndrome progeroid type
Homo sapiens (human)
DOID:0080201
  • Peters plus syndrome
  • Aliases:
    • Krause-Kivlin syndrome
    • Peters anomaly-short limb dwarfism syndrome
    • Peters-plus syndrome
Homo sapiens (human)
DOID:0111230
  • congenital muscular dystrophy-dystroglycanopathy type A11
  • Aliases:
    • MDDGA11
    • Walker-Warburg syndrome or muscle-eye-brain disease B3GALNT2-related
    • congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A11
Homo sapiens (human)
DOID:1088
  • meningocele
Homo sapiens (human)
DOID:2303
  • stereotypic movement disorder
  • Aliases:
    • Stereotyped repetitive movements
    • Stereotypy habit disorder
Homo sapiens (human)
DOID:0110881
  • holoprosencephaly 1
  • Aliases:
    • HPE1
Homo sapiens (human)
DOID:4621
  • holoprosencephaly
  • Aliases:
    • Holoprosencephaly sequence
Homo sapiens (human)
DOID:0050559
  • Fukuyama congenital muscular dystrophy
Homo sapiens (human)
DOID:0060673
  • Peters anomaly
Homo sapiens (human)
DOID:0060287
  • cornea plana
  • Aliases:
    • flat cornea
Homo sapiens (human)
DOID:0110004
  • 3-methylglutaconic aciduria type 3
  • Aliases:
    • 3-methylglutaconic aciduria type III
    • Costeff optic atrophy syndrome
    • Costeff syndrome
    • Iraqi-Jewish optic atrophy plus
    • MGA3
    • autosomal recessive optic atrophy plus syndrome
    • autosomal recessive optic atrophy type 3
    • infantile optic atrophy with chorea and spastic paraplegia
Homo sapiens (human)
DOID:0050476
  • Barth syndrome
  • Aliases:
    • 3-methylglutaconicaciduria type 2
    • 3-methylglutaconicaciduria type II
    • MGA Type 2
    • MGA type II
Homo sapiens (human)
DOID:12397
  • entropion
Homo sapiens (human)
DOID:0112275
  • developmental and epileptic encephalopathy 93
  • Aliases:
    • DEE93
    • IECEE3
    • infantile or early childhood epileptic encephalopathy 3
Homo sapiens (human)
DOID:1759
  • American histoplasmosis
Homo sapiens (human)
DOID:10348
  • blepharophimosis
Homo sapiens (human)
DOID:8466
  • retinal degeneration
  • Aliases:
    • degeneration of retina
Homo sapiens (human)
DOID:0110942
  • autosomal recessive osteopetrosis 1
  • Aliases:
    • OPTB1
    • autosomal recessive Albers-Schonberg disease
    • infantile malignant osteopetrosis 1
Homo sapiens (human)
DOID:0112171
  • wrinkly skin syndrome
  • Aliases:
    • WSS
Homo sapiens (human)
DOID:12053
  • cryptococcosis
  • Aliases:
    • Busse-Buschke's disease
    • European cryptococcosis
    • cryptococcal infection
    • torula
    • torulosis
Homo sapiens (human)

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024