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 4926 - 4950 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼
DOID:6868
  • mediastinal malignant lymphoma
  • Aliases:
    • Lymphoma of mediastinum
Homo sapiens (human)
DOID:0110108
  • atrial heart septal defect 3
  • Aliases:
    • ASD3
    • atrial septal defect 3
Homo sapiens (human)
DOID:0110848
  • xeroderma pigmentosum group F
  • Aliases:
    • XP group F
    • XP6
    • XPF
    • xeroderma pigmentosum VI
Homo sapiens (human)
DOID:5766
  • pulmonary sclerosing hemangioma
  • Aliases:
    • Pneumocytoma
Homo sapiens (human)
DOID:0060022
  • CD40 ligand deficiency
  • Aliases:
    • HIGMX-1
    • X-linked hyper-IgM syndrome
Homo sapiens (human)
DOID:0060540
  • Hermansky-Pudlak syndrome 2
Homo sapiens (human)
DOID:0080349
  • developmental and epileptic encephalopathy 39
  • Aliases:
    • AGC1 deficiency
    • early infantile epileptic encephalopathy 39
    • epileptic encephalopathy with global cerebral demyelination
Homo sapiens (human)
DOID:4916
  • pituitary carcinoma
  • Aliases:
    • carcinoma of the Pituitary gland
Homo sapiens (human)
DOID:0110658
  • congenital myasthenic syndrome 15
  • Aliases:
    • CMS15
    • congenital myasthenic syndrome 15 without tubular aggregates
Homo sapiens (human)
DOID:0060276
  • pontocerebellar hypoplasia type 7
Homo sapiens (human)
DOID:0110194
  • Charcot-Marie-Tooth disease type 4B3
  • Aliases:
    • CMT4B3
Homo sapiens (human)
DOID:11257
  • social phobia
Homo sapiens (human)
DOID:0110045
  • Alzheimer's disease 12
  • Aliases:
    • AD12
    • Alzheimer disease 12
    • Alzheimer disease familial 12
Homo sapiens (human)
DOID:0111260
  • phosphoribosylpyrophosphate synthetase superactivity
  • Aliases:
    • PRPP synthetase superactivity
    • PRPS1 superactivity
Homo sapiens (human)
DOID:0081183
  • autosomal recessive intellectual developmental disorder 7
Homo sapiens (human)
DOID:0050813
  • spondyloepiphyseal dysplasia with congenital joint dislocations
  • Aliases:
    • CHONDRODYSPLASIA WITH MULTIPLE DISLOCATIONS
    • CHST3-Related Skeletal Dysplasia
    • Humero-spinal dysostosis with congenital heart disease
    • Kozlowski Celermajer Tink syndrome
    • Omani Type
    • Spondyloepiphyseal Dysplasia
    • humero-spinal dysostosis
    • humerospinal dysostosis
Homo sapiens (human)
DOID:0111422
  • familial lipase maturation factor 1 deficiency
  • Aliases:
    • LPL and HL deficiency
    • LPL and HTGL deficiency
    • combined lipase deficiency
    • familial LMF1 deficiency
    • lipoprotein lipase deficiency with hepatic triglyceride lipase deficiency
Homo sapiens (human)
DOID:0110476
  • autosomal recessive nonsyndromic deafness 1B
  • Aliases:
    • DFNB1B
    • autosomal recessive deafness 1B
Homo sapiens (human)
DOID:1921
  • Klinefelter syndrome
  • Aliases:
    • 47, XXY
    • Hypogonadotropic Hypogonadism
    • Klinefelter's syndrome
    • XXY syndrome
    • XXY trisomy
Homo sapiens (human)
DOID:0090037
  • torsion dystonia 13
Homo sapiens (human)
DOID:0080738
  • Ehlers-Danlos syndrome spondylodysplastic type 1
Homo sapiens (human)
DOID:2348
  • arteriosclerotic cardiovascular disease
  • Aliases:
    • Cardiovascular arteriosclerosis
Homo sapiens (human)
DOID:355
  • mast-cell sarcoma
Homo sapiens (human)
DOID:13724
  • scurvy
Homo sapiens (human)
DOID:8719
  • in situ carcinoma
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