GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB), DisGeNET, and Alliance of Genome Resources is integrated into one list.

Source Last Updated
Alliance of Genome Resources July 29, 2024
DisGeNET July 29, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 4276 - 4300 of 4621 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲
DOID:0110785
  • hereditary spastic paraplegia 34
  • Aliases:
    • SPG34
    • X-linked spastic paraplegia 34
    • X-linked spastic paraplegia type 34
Homo sapiens (human)
DOID:0080548
  • Noonan syndrome with multiple lentigines 1
  • Aliases:
    • LEOPARD syndrome 1
Homo sapiens (human)
DOID:3904
  • bronchus carcinoma
  • Aliases:
    • BC - Bronchogenic carcinoma
Homo sapiens (human)
DOID:0060642
  • recessive dystrophic epidermolysis bullosa
  • Aliases:
    • RDEB, Hallopeau-Siemens type
    • autosomal recessive dystrophic epidermolysis bullosa generalisata gravis
    • autosomal recessive dystrophic epidermolysis bullosa, Hallopeau-Siemens type
Homo sapiens (human)
DOID:9893
  • periodontosis
Homo sapiens (human)
DOID:0081180
  • autosomal recessive intellectual developmental disorder 12
Homo sapiens (human)
DOID:5525
  • anal squamous cell carcinoma
  • Aliases:
    • Epidermoid anal carcinoma
Homo sapiens (human)
DOID:0090024
  • split hand-foot malformation 1 with sensorineural hearing loss
  • Aliases:
    • SHFM1D
    • congenital deafness with split hands and feet
Homo sapiens (human)
DOID:12783
  • migraine without aura
  • Aliases:
    • common migraine
Homo sapiens (human)
DOID:11400
  • pyelonephritis
Homo sapiens (human)
DOID:0110763
  • hereditary spastic paraplegia 10
  • Aliases:
    • SPG10
    • autosomal dominant spastic paraplegia 10
    • autosomal dominant spastic paraplegia type 10
Homo sapiens (human)
DOID:1564
  • fungal infectious disease
  • Aliases:
    • mycosis
Homo sapiens (human)
DOID:10273
  • heart conduction disease
  • Aliases:
    • heart rhythm disease
Homo sapiens (human)
DOID:5138
  • leiomyomatosis
Homo sapiens (human)
DOID:8533
  • hypopharynx cancer
  • Aliases:
    • Hypopharyngeal cancer
    • malignant Hypopharyngeal tumor
    • malignant neoplasm of hypopharynx
    • malignant tumor of hypopharynx
    • malignant tumour of hypopharynx
Homo sapiens (human)
DOID:3372
  • chondroblastic osteosarcoma
  • Aliases:
    • chondrosarcomatous Osteogenic sarcoma
Homo sapiens (human)
DOID:0050589
  • inflammatory bowel disease
Homo sapiens (human)
DOID:11729
  • Lyme disease
  • Aliases:
    • Bannwarth syndrome
    • Bannworth's syndrome
    • Lyme borreliosis
    • Neurological Lyme disease
    • lyme neuroborreliosis
    • neuroborreliosis
Homo sapiens (human)
DOID:0110765
  • hereditary spastic paraplegia 12
  • Aliases:
    • SPG12
    • autosomal dominant spastic paraplegia 12
    • autosomal dominant spastic paraplegia type 12
Homo sapiens (human)
DOID:10969
  • hemiplegia
  • Aliases:
    • Infantile hemiplegia
    • Postnatal infantile hemiplegia
Homo sapiens (human)
DOID:0112233
  • lissencephaly 8
  • Aliases:
    • LIS8
Homo sapiens (human)
DOID:4964
  • neurotic disorder
  • Aliases:
    • Neurotic depression reactive type
    • Neurotic depressive state
    • Psychoneurosis
    • depressive neurosis
    • neurosis
    • neurotic depression
    • reactive depression
Homo sapiens (human)
DOID:14679
  • VACTERL association
Homo sapiens (human)
DOID:0111045
  • platelet-type bleeding disorder 9
  • Aliases:
    • BDPLT9
    • GP Ia deficiency
    • collagen platelet receptor deficiency
    • glycoprotein Ia deficiency
Homo sapiens (human)
DOID:9266
  • cystinuria
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