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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 January 28, 2025
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 2526 - 2550 of 4115 in total
Disease ID Disease Name ▲ Gene Symbol Gene ID Organism Source
DOID:4195
  • hyperglycemia
Homo sapiens (human)
DOID:9279
  • hyperhomocysteinemia
Homo sapiens (human)
DOID:2959
  • hyperimmunoglobulin syndrome
Homo sapiens (human)
DOID:0081450
  • hyperimmunoglobulinemia D periodic fever syndrome
  • Aliases:
    • HYPER-IgD SYNDROME
Homo sapiens (human)
DOID:2018
  • hyperinsulinism
  • Aliases:
    • hyperinsulinemia
Homo sapiens (human)
DOID:14451
  • hyperkalemic periodic paralysis
  • Aliases:
    • familial hyperkalemic periodic paralysis
Homo sapiens (human)
DOID:3145
  • hyperlipoproteinemia type III
  • Aliases:
    • Remnant hyperlipidemia
    • carbohydrate induced hyperlipemia
    • familial hypercholesterolaemia with hyperlipaemia
    • familial type 3 hyperlipoproteinemia
Homo sapiens (human)
DOID:1172
  • hyperlipoproteinemia type IV
  • Aliases:
    • Endogenous hyperlipidaemia
    • Fredrickson type IV Lipidemia
    • Fredrickson type IV hyperlipoproteinemia
    • Fredrickson type IV lipidaemia
    • VLDL hyperlipoproteinemia
    • familial hypertriglyceridemia
Homo sapiens (human)
DOID:1171
  • hyperlipoproteinemia type V
  • Aliases:
    • Fredrickson type V lipaemia
    • familial hyperlipoproteinemia type V
    • familial type 5 hyperlipoproteinemia
Homo sapiens (human)
DOID:0080537
  • hypermanganesemia with dystonia 2
Homo sapiens (human)
DOID:0111039
  • hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase
  • Aliases:
    • hypermethioninemia due to S-adenosylhomocysteine hydrolase deficiency
    • psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency
Homo sapiens (human)
DOID:9834
  • hyperopia
  • Aliases:
    • Far-sightedness
    • farsightedness
    • hypermetropia
Homo sapiens (human)
DOID:13543
  • hyperparathyroidism
Homo sapiens (human)
DOID:0070433
  • hyperphosphatasia with impaired intellectual development syndrome 1
  • Aliases:
    • GPIBD2
    • HPMRS1
    • glycosylphosphatidylinositol biosynthesis defect 2
    • hyperphosphatasia with mental retardation syndrome 1
Homo sapiens (human)
DOID:0070434
  • hyperphosphatasia with impaired intellectual development syndrome 2
  • Aliases:
    • GPIBD6
    • HPMRS2
    • glycosylphosphatidylinositol biosynthesis defect 6
    • hyperphosphatasia with mental retardation syndrome 2
Homo sapiens (human)
DOID:0070435
  • hyperphosphatasia with impaired intellectual development syndrome 3
  • Aliases:
    • GPIBD8
    • HPMRS3
    • glycosylphosphatidylinositol biosynthesis defect 8
    • hyperphosphatasia with mental retardation syndrome 3
Homo sapiens (human)
DOID:0070436
  • hyperphosphatasia with impaired intellectual development syndrome 4
  • Aliases:
    • GPIBD62
    • HPMRS6
    • glycosylphosphatidylinositol biosynthesis defect 62
    • hyperphosphatasia with mental retardation syndrome 6
Homo sapiens (human)
DOID:0070432
  • hyperphosphatasia with impaired intellectual development syndrome 5
  • Aliases:
    • GPIBD11
    • HPMRS5
    • glycosylphosphatidylinositol biosynthesis defect 11
    • hyperphosphatasia with mental retardation syndrome 5
Homo sapiens (human)
DOID:0070437
  • hyperphosphatasia with impaired intellectual development syndrome 6
  • Aliases:
    • GPIBD40
    • HPMRS4
    • glycosylphosphatidylinositol biosynthesis defect 40
    • hyperphosphatasia with mental retardation syndrome 4
Homo sapiens (human)
DOID:0111063
  • hyperphosphatemic familial tumoral calcinosis
  • Aliases:
    • HFTC
    • PHPTC
    • cortical hyperostosis with hyperphosphatemia
    • familial Teutschlaender disease
    • familial hyperphosphatemic tumoral calcinosis/hyperphosphatemic hyperostosis syndrome
    • hypercalcemic tumoral calcinosis
    • hyperostosis with hyperphosphatemia
    • hyperphosphatemia hyperostosis
    • hyperphosphatemia hyperostosis syndrome
    • hyperphosphatemia tumoral calcinosis
    • lipocalcinogranulomatosis
    • morbus Teutschlaender
    • primary hyperphosphatemic tumoral calcinosis
    • tumoral calcinosis with hyperphosphatemia
Homo sapiens (human)
DOID:12700
  • hyperprolactinemia
  • Aliases:
    • Chiari-Frommel syndrome
    • Pregnancy-related A-G syndrome
    • hyperprolactinaemia
Homo sapiens (human)
DOID:0111247
  • hypertension and brachydactyly syndrome
  • Aliases:
    • Bilginturan brachydactyly
    • Bilginturan syndrome
    • HTNB
    • brachydactyly with hypertension
    • type E brachydactyly with short stature and hypertension
Homo sapiens (human)
DOID:10763
  • hypertension
  • Aliases:
    • HTN
    • hyperpiesia
    • vascular hypertensive disorder
Homo sapiens (human)
DOID:7998
  • hyperthyroidism
  • Aliases:
    • overactive thyroid
Homo sapiens (human)
DOID:2855
  • hyperthyroxinemia
Homo sapiens (human)
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Last updated: April 7, 2025