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 July 29, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 4051 - 4075 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼
DOID:0110218
  • Brugada syndrome 1
  • Aliases:
    • BRGDA1
Homo sapiens (human)
DOID:203
  • exostosis
  • Aliases:
    • bone spur
    • bony outgrowth
    • orbital exostosis
    • osteophyte
    • swimmer's exostosis
Homo sapiens (human)
DOID:1380
  • endometrial cancer
  • Aliases:
    • endometrial Ca
    • endometrial neoplasm
    • malignant endometrial neoplasm
    • malignant neoplasm of endometrium
    • neoplasm of endometrium
    • primary malignant neoplasm of endometrium
    • tumor of Endometrium
Homo sapiens (human)
DOID:8692
  • myeloid leukemia
  • Aliases:
    • Non-Lymphocytic Leukemia
    • leukaemia myelogenous
    • leukemia myelogenous
    • myeloid granulocytic leukaemia
    • myeloid granulocytic leukemia
    • myeloid leukaemia
Homo sapiens (human)
DOID:3413
  • alpha-mannosidosis
  • Aliases:
    • Alpha-D-mannosidosis
    • alpha-mannosidase deficiency
    • deficiency of alpha-mannosidase
Homo sapiens (human)
DOID:0110793
  • hereditary spastic paraplegia 41
  • Aliases:
    • SPG41
    • autosomal dominant spastic paraplegia 41
    • autosomal dominant spastic paraplegia type 41
Homo sapiens (human)
DOID:684
  • hepatocellular carcinoma
  • Aliases:
    • Hepatoma
Homo sapiens (human)
DOID:4767
  • classic pulmonary blastoma
Homo sapiens (human)
DOID:10974
  • oophoritis
Homo sapiens (human)
DOID:6620
  • X-linked hyper IgM syndrome
  • Aliases:
    • HIGM1
    • X-linked hyper-IgM immunodeficiency
    • XHIM
    • hyper-IgM immunodeficiency syndrome type 1
    • hyper-IgM syndrome 1
    • hyper-IgM syndrome type 1
    • immunodeficiency with hyper-IgM type 1
Homo sapiens (human)
DOID:171
  • neuroectodermal tumor
  • Aliases:
    • primitive Neuroectodermal neoplasm
Homo sapiens (human)
DOID:0080950
  • alopecia-mental retardation syndrome 4
Homo sapiens (human)
DOID:1060
  • Hartnup disease
  • Aliases:
    • Neutral 1 amino acid transport defect
    • deficiency of tryptophan oxygenase
    • neutral amino acid transport defect
Homo sapiens (human)
DOID:14269
  • suppurative cholangitis
Homo sapiens (human)
DOID:0080334
  • aortic valve disease 2
Homo sapiens (human)
DOID:0110250
  • cataract 16 multiple types
  • Aliases:
    • CTRCT16
Homo sapiens (human)
DOID:0110870
  • congenital stationary night blindness 1A
  • Aliases:
    • CSNB1A
    • NBMI
    • complete CSNB X-linked
    • congenital stationary night blindness 1A X-linked
    • congenital stationary night blindness with myopia
    • hemeralopia-myopia
    • myopia-night blindness
Homo sapiens (human)
DOID:0112171
  • wrinkly skin syndrome
  • Aliases:
    • WSS
Homo sapiens (human)
DOID:4184
  • pseudohypoparathyroidism
Homo sapiens (human)
DOID:327
  • syringomyelia
Homo sapiens (human)
DOID:5769
  • verruciform xanthoma of skin
  • Aliases:
    • Cutaneous Verruciform Xanthoma
    • Verruciform xanthoma
Homo sapiens (human)
DOID:5746
  • ovarian serous cystadenocarcinoma
  • Aliases:
    • serous cystadenoma
Homo sapiens (human)
DOID:0110114
  • atrial heart septal defect 9
  • Aliases:
    • ASD9
    • atrial septal defect 9
Homo sapiens (human)
DOID:0070116
  • Meckel syndrome 2
  • Aliases:
    • MKS2
    • Meckel-Gruber syndrome, type 2
Homo sapiens (human)
DOID:0111120
  • nephronophthisis 9
  • Aliases:
    • NPHP9
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