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 776 - 800 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Organism Source
DOID:2154
  • nephroblastoma
  • Aliases:
    • adult nephroblastoma
Homo sapiens (human)
DOID:5409
  • lung small cell carcinoma
Homo sapiens (human)
DOID:2920
  • membranoproliferative glomerulonephritis
  • Aliases:
    • Lobular glomerulonephritis
    • chronic glomerulonephritis, lobular
Homo sapiens (human)
DOID:8552
  • chronic myeloid leukemia
  • Aliases:
    • CML
    • CML - chronic Myelogenous Leukemia
    • Myeloid Leukemia, chronic
    • chronic granulocytic leukaemia
    • chronic granulocytic leukemia
    • chronic myelogenous leukaemia
    • chronic myelogenous leukemia
    • chronic myeloid leukaemia
Homo sapiens (human)
DOID:8634
  • prostate carcinoma in situ
  • Aliases:
    • PIN III
    • carcinoma in situ of prostate
    • grade III PIN
Homo sapiens (human)
DOID:5223
  • infertility
Homo sapiens (human)
DOID:0050773
  • paraganglioma
  • Aliases:
    • chemodectoma
    • glomus body tumor
Homo sapiens (human)
DOID:9669
  • senile cataract
Homo sapiens (human)
DOID:3125
  • multiple endocrine neoplasia
  • Aliases:
    • Multiple endocrine adenomatosis
    • Multiple endocrine neoplasia syndrome
Homo sapiens (human)
DOID:3829
  • pituitary adenoma
  • Aliases:
    • adenoma of the Pituitary gland
Homo sapiens (human)
DOID:0080137
  • multiple endocrine neoplasia type 4
  • Aliases:
    • Multiple Endocrine Neoplasia, Type IV
Homo sapiens (human)
DOID:0080238
  • autosomal dominant intellectual developmental disorder 47
  • Aliases:
    • autosomal dominant mental retardation 47
Homo sapiens (human)
DOID:10584
  • retinitis pigmentosa
  • Aliases:
    • pericentral pigmentary retinopathy
Homo sapiens (human)
DOID:1059
  • intellectual disability
Mus musculus (house mouse)
DOID:1824
  • status epilepticus
  • Aliases:
    • Grand mal status
Mus musculus (house mouse)
DOID:0050800
  • cerebral creatine deficiency syndrome 1
  • Aliases:
    • CEREBRAL CREATINE DEFICIENCY SYNDROME 1
    • SLC6A8 deficiency
    • creatine transporter deficiency
Mus musculus (house mouse)
DOID:11476
  • osteoporosis
Mus musculus (house mouse)
DOID:12858
  • Huntington's disease
  • Aliases:
    • HD
    • Huntington disease
    • Huntington's chorea
Mus musculus (house mouse)
DOID:3827
  • congenital diaphragmatic hernia
  • Aliases:
    • Diaphragmatic Hernia
Mus musculus (house mouse)
DOID:0111222
  • centronuclear myopathy 5
  • Aliases:
    • CNM5
Homo sapiens (human)
DOID:0070005
  • Seckel syndrome 9
  • Aliases:
    • SCKL9
Homo sapiens (human)
DOID:0090131
  • complex cortical dysplasia with other brain malformations
  • Aliases:
    • CDCBM
Homo sapiens (human)
DOID:0080409
  • familial adenomatous polyposis 1
Homo sapiens (human)
DOID:0081218
  • autosomal recessive intellectual developmental disorder 74
Homo sapiens (human)
DOID:0112104
  • Sotos syndrome 3
  • Aliases:
    • SOTOS3
Homo sapiens (human)

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Last updated: December 9, 2024