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 4176 - 4200 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼
DOID:8743
  • erythema infectiosum
  • Aliases:
    • Fifth disease
Homo sapiens (human)
DOID:0110164
  • Charcot-Marie-Tooth disease type 2D
  • Aliases:
    • CMT2D
    • Charcot-Marie-Tooth disease neuronal type 2D
    • Charcot-Marie-Tooth neuropathy type 2D
    • autosomal dominant Charcot-Marie-Tooth disease type 2D
Homo sapiens (human)
DOID:2536
  • chronic inflammatory demyelinating polyneuritis
Homo sapiens (human)
DOID:0110031
  • hemoglobin H disease
  • Aliases:
    • HBH
    • alpha thalassemia, haemoglobin H type
    • alpha thalassemia, hemoglobin H type
    • alpha-thalassemia intermedia
    • haemoglobin H disease
    • haemoglobin H disease, deletional
    • hemoglobin H disease, deletional
Homo sapiens (human)
DOID:0060216
  • Cogan syndrome
  • Aliases:
    • Cogan's syndrome
    • diffuse interstitual keratitis
Homo sapiens (human)
DOID:5509
  • childhood ependymoma
Homo sapiens (human)
DOID:0110279
  • autosomal recessive limb-girdle muscular dystrophy type 2E
  • Aliases:
    • Beta-sarcoglycanopathy
    • LGMD2E
    • Limb-girdle muscular dystrophy due to beta-sarcoglycan deficiency
    • muscular dystrophy, limb-girdle, type 2E
Homo sapiens (human)
DOID:4080
  • tricuspid valve insufficiency
  • Aliases:
    • Tricuspid incompetence
    • Tricuspid regurgitation
    • Tricuspid valve regurgitation
Homo sapiens (human)
DOID:0111071
  • congenital bile acid synthesis defect 1
  • Aliases:
    • CBAS1
Homo sapiens (human)
DOID:1856
  • cherubism
Homo sapiens (human)
DOID:2007
  • degeneration of macula and posterior pole
  • Aliases:
    • degeneration of macula and posterior pole of retina
    • degeneration of macula or posterior pole
Homo sapiens (human)
DOID:0050883
  • infantile cerebellar-retinal degeneration
Homo sapiens (human)
DOID:10933
  • obsessive-compulsive disorder
  • Aliases:
    • Anancastic neurosis
    • obsessive compulsive disorder
Homo sapiens (human)
DOID:1474
  • aggressive periodontitis
  • Aliases:
    • juvenile periodontitis
Homo sapiens (human)
DOID:10493
  • adrenal cortical hypofunction
  • Aliases:
    • Adrenal Cortical Insufficiency
    • Corticoadrenal insufficiency
Homo sapiens (human)
DOID:11661
  • blue color blindness
  • Aliases:
    • Tritan defect
    • Tritanopia
Homo sapiens (human)
DOID:12145
  • detrusor sphincter dyssynergia
Homo sapiens (human)
DOID:2152
  • ovary epithelial cancer
  • Aliases:
    • Ovarian Surface epithelial-Stromal tumor
Homo sapiens (human)
DOID:10937
  • impulse control disorder
Homo sapiens (human)
DOID:0070127
  • congenital nongoitrous hypothyroidism 3
  • Aliases:
    • CHNG3
Homo sapiens (human)
DOID:0110191
  • Charcot-Marie-Tooth disease type 4B1
  • Aliases:
    • CMT4B1
    • Charcot-Marie-Tooth neuropathy type 4B1
    • autosomal recessive Charcot-Marie-Tooth disease with focally folded myelin sheaths type 4B1
Homo sapiens (human)
DOID:2326
  • gastroenteritis
  • Aliases:
    • cholera morbus
    • infectious colitis, enteritis and gastroenteritis
Homo sapiens (human)
DOID:615
  • leukopenia
  • Aliases:
    • Leucopenia
Homo sapiens (human)
DOID:0081427
  • autosomal recessive distal hereditary motor neuronopathy 8
  • Aliases:
    • SORDD
    • sorbitol dehydrogenase deficiency with peripheral neuropathy
Homo sapiens (human)
DOID:0060699
  • familial hypocalciuric hypercalcemia
  • Aliases:
    • FBH
    • FBHH
    • FHH
    • familial benign hypercalcemia
    • familial benign hypocalciuric hypercalcemia
Homo sapiens (human)

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Supported by JST NBDC Grant Number JPMJND2204

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Last updated: August 19, 2024