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 6826 - 6850 of 7942 in total
Disease ID Disease Name ▼ Gene Symbol Gene ID Organism
DOID:13072
  • acquired hyperkeratosis
  • Aliases:
    • Keratoderma - acquired
    • Keratoderma, acquired
    • acquired keratoderma
Homo sapiens (human)
DOID:13912
  • acquired color blindness
  • Aliases:
    • acquired color vision deficiencies
    • acquired color vision deficiency
    • acquired colour blindness
    • acquired colour vision deficiencies
    • acquired colour vision deficiency
Homo sapiens (human)
DOID:0080941
  • acquired angioedema
Homo sapiens (human)
DOID:12689
  • acoustic neuroma
  • Aliases:
    • Vestibular Neurilemmoma
    • Vestibular schwannoma
Homo sapiens (human)
DOID:6543
  • acne
  • Aliases:
    • Acne varioliformis
    • acne vulgaris
    • frontalis acne
Homo sapiens (human)
DOID:6543
  • acne
  • Aliases:
    • Acne varioliformis
    • acne vulgaris
    • frontalis acne
Rattus norvegicus (Norway rat)
DOID:6543
  • acne
  • Aliases:
    • Acne varioliformis
    • acne vulgaris
    • frontalis acne
Mus musculus (house mouse)
DOID:3025
  • acinar cell carcinoma
  • Aliases:
    • acinic cell carcinoma
Homo sapiens (human)
DOID:5392
  • acidophil adenoma
  • Aliases:
    • Eosinophil adenoma
Homo sapiens (human)
DOID:13911
  • achromatopsia
  • Aliases:
    • ACHM
    • Monochromatism
Homo sapiens (human)
DOID:0110008
  • achromatopsia 3
  • Aliases:
    • ACHM1
    • ACHM3
    • Pingelapese blindness
    • RMCH1
    • rod monochromacy 1
    • rod monochromatism 1
Homo sapiens (human)
DOID:4480
  • achondroplasia
  • Aliases:
    • Achondroplastic physique
    • Chondrodystrophia
    • osteosclerosis congenita
Homo sapiens (human)
DOID:0080055
  • achondrogenesis type IB
  • Aliases:
    • achondrogenesis Fraccaro type
Homo sapiens (human)
DOID:9164
  • achalasia
  • Aliases:
    • Lack of reflex relaxation of lower oesophageal sphincter
    • achalasia of cardia
    • achalasia of esophagus
    • cardiospasm
    • esophageal achalasia
    • hypertensive lower esophageal sphincter
Homo sapiens (human)
DOID:9839
  • accommodative esotropia
Homo sapiens (human)
DOID:2582
  • acatalasia
  • Aliases:
    • acatalasemia
    • deficiency of catalase
Homo sapiens (human)
DOID:3138
  • acanthosis nigricans
  • Aliases:
    • keratosis nigricans
Homo sapiens (human)
DOID:0070309
  • absence epilepsy
Homo sapiens (human)
DOID:0060550
  • ablepharon macrostomia syndrome
Homo sapiens (human)
DOID:1386
  • abetalipoproteinemia
  • Aliases:
    • familial hypobetalipoproteinemia
    • microsomal triglyceride transfer protein deficiency disease
Homo sapiens (human)
DOID:0060611
  • abdominal obesity-metabolic syndrome
Homo sapiens (human)
DOID:0060611
  • abdominal obesity-metabolic syndrome
Rattus norvegicus (Norway rat)
DOID:0060611
  • abdominal obesity-metabolic syndrome
Mus musculus (house mouse)
DOID:14221
  • abdominal obesity-metabolic syndrome 1
  • Aliases:
    • dysmetabolic syndrome X
    • metabolic syndrome X
Mus musculus (house mouse)
DOID:14221
  • abdominal obesity-metabolic syndrome 1
  • Aliases:
    • dysmetabolic syndrome X
    • metabolic syndrome X
Homo sapiens (human)

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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