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 2226 - 2250 of 4621 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism
DOID:13374
  • fibrodysplasia ossificans progressiva
  • Aliases:
    • Stone Man Syndrome
    • myositis ossificans progressiva
    • progressive myositis ossificans
    • progressive ossifying myositis
Homo sapiens (human)
DOID:668
  • myositis ossificans
  • Aliases:
    • Myisitis ossificans
    • Ossification - muscle
Homo sapiens (human)
DOID:0111253
  • neurofibromatosis 1
  • Aliases:
    • NF1
    • Peripheral Neurofibromatosis
    • Recklinghausen's neurofibromatosis
    • neurofibromatosis type I
    • von Recklinghausen Disease
Homo sapiens (human)
DOID:4647
  • trilateral retinoblastoma
Homo sapiens (human)
DOID:4648
  • familial retinoblastoma
  • Aliases:
    • Hereditary Retinoblastoma
Homo sapiens (human)
DOID:2772
  • irritant dermatitis
  • Aliases:
    • irritant contact dermatitis
    • primary irritant dermatitis
Homo sapiens (human)
DOID:3973
  • thyroid gland medullary carcinoma
  • Aliases:
    • Medullary carcinoma of the Thyroid gland
    • Ultimobranchial thyroid tumor
    • Ultimobranchial thyroid tumour
    • medullary thyroid carcinoma
Homo sapiens (human)
DOID:0050471
  • Carney complex
  • Aliases:
    • Carney Complex, Type 1
    • Carney Complex, Type 2
    • Carney Syndrome
    • Carney complex variant
    • LAMB Syndrome
    • NAME Syndrome
Homo sapiens (human)
DOID:0050523
  • adult T-cell leukemia/lymphoma
  • Aliases:
    • Adult T-cell leukemia/lymphoma (HTLV-1 positive)
    • adult T-cell leukemia
Homo sapiens (human)
DOID:12156
  • arachnoiditis
Homo sapiens (human)
DOID:9471
  • meningitis
Homo sapiens (human)
DOID:8712
  • neurofibromatosis
Homo sapiens (human)
DOID:0080070
  • mucolipidosis II alpha/beta
  • Aliases:
    • I-cell disease
    • inclusion-cell disease
    • mucolipidosis II
Homo sapiens (human)
DOID:3343
  • glycoproteinosis
  • Aliases:
    • Mucolipidosis type I
    • sialidosis
Homo sapiens (human)
DOID:0110219
  • Brugada syndrome 2
  • Aliases:
    • BRGDA2
Homo sapiens (human)
DOID:0110218
  • Brugada syndrome 1
  • Aliases:
    • BRGDA1
Homo sapiens (human)
DOID:0110224
  • Brugada syndrome 7
  • Aliases:
    • BRGDA7
Homo sapiens (human)
DOID:0110220
  • Brugada syndrome 3
  • Aliases:
    • BRGDA3
Homo sapiens (human)
DOID:0050451
  • Brugada syndrome
  • Aliases:
    • Bangungut
    • Brugada type idiopathic ventricular fibrillation
    • Dream disease
    • Pokkuri death syndrome
    • SUNDS
    • sudden unexplained nocturnal death syndrome
Homo sapiens (human)
DOID:0110223
  • Brugada syndrome 6
  • Aliases:
    • BRGDA6
Homo sapiens (human)
DOID:0110225
  • Brugada syndrome 8
  • Aliases:
    • BRGDA8
Homo sapiens (human)
DOID:0110222
  • Brugada syndrome 5
  • Aliases:
    • BRGDA5
Homo sapiens (human)
DOID:0110221
  • Brugada syndrome 4
  • Aliases:
    • BRGDA4
Homo sapiens (human)
DOID:0110226
  • Brugada syndrome 9
  • Aliases:
    • BRGDA9
Homo sapiens (human)
DOID:0080031
  • fibrous dysplasia
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