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 801 - 825 of 4621 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲
DOID:1909
  • melanoma
  • Aliases:
    • Naevocarcinoma
    • malignant melanoma
Homo sapiens (human)
DOID:10811
  • nasal cavity cancer
  • Aliases:
    • malignant neoplasm of nasal cavities
    • malignant tumor of the nasal cavity
Homo sapiens (human)
DOID:1768
  • conversion disorder
  • Aliases:
    • Conversion Hysterical Neurosis
    • Conversion hysteria or reaction
    • Hysterical neurosis, conversion type
Homo sapiens (human)
DOID:14686
  • Axenfeld-Rieger syndrome
  • Aliases:
    • Anomaly, Rieger's
    • Axenfeld syndrome
    • RGS - Rieger syndrome
    • Rieger's anomaly
Homo sapiens (human)
DOID:1143
  • exotropia
  • Aliases:
    • Divergent Strabismus
    • Divergent concomitant strabismus
Homo sapiens (human)
DOID:9768
  • heart aneurysm
  • Aliases:
    • cardiac aneurysm
Homo sapiens (human)
DOID:0070119
  • Meckel syndrome 5
  • Aliases:
    • MKS5
    • Meckel-Gruber syndrome, type 5
Homo sapiens (human)
DOID:0110724
  • neuronal ceroid lipofuscinosis 8 northern epilepsy variant
  • Aliases:
    • EPMR
    • northern epilepsy variant, neuronal ceroid lipofuscinosis, Northern epilepsy variant
    • progressive epilepsy with mental retardation, northern epilepsy
    • progressive epilepsy-intellectual disability syndrome, Finnish type
Homo sapiens (human)
DOID:5246
  • obsolete hilar cholangiocellular carcinoma
Homo sapiens (human)
DOID:0110212
  • Charcot-Marie-Tooth disease X-linked recessive 4
  • Aliases:
    • CMT4X
    • CMTX4
    • Charcot-Marie-Tooth disease with deafness and mental retardation
    • Cowchock syndrome
    • NADMR
    • NAMSD
    • X-linked Charcot-Marie-Tooth disease type 4
    • axonal motor sensory neuropathy with deafness and mental retardation
Homo sapiens (human)
DOID:0060254
  • Robinow syndrome
  • Aliases:
    • Robinow dwarfism
    • acral dysostosis with facial and genital abnormalities
    • fetal face syndrome
Homo sapiens (human)
DOID:9351
  • diabetes mellitus
  • Aliases:
    • diabetes
Homo sapiens (human)
DOID:4948
  • gallbladder carcinoma
  • Aliases:
    • cancer of the gallbladder
    • carcinoma gallbladder
    • carcinoma of gallbladder
Homo sapiens (human)
DOID:4031
  • eosinophilic gastroenteritis
Homo sapiens (human)
DOID:9503
  • Loeffler syndrome
  • Aliases:
    • Loeffler's pneumonia
    • Loffler's syndrome
Homo sapiens (human)
DOID:0110459
  • dilated cardiomyopathy 1FF
  • Aliases:
    • CMD1FF
Homo sapiens (human)
DOID:0050456
  • Buruli ulcer disease
  • Aliases:
    • Bairnsdale ulcer
    • Daintree ulcer
    • Mossman ulcer
    • Searl ulcer
    • Searle's ulcer
Homo sapiens (human)
DOID:0110511
  • autosomal recessive nonsyndromic deafness 59
  • Aliases:
    • DFNB59
    • autosomal recessive deafness 59
Homo sapiens (human)
DOID:0080159
  • Cryptococcal meningitis
Homo sapiens (human)
DOID:7165
  • subacute thyroiditis
  • Aliases:
    • De Quervain's thyroiditis
    • Giant-cell thyroiditis
    • Granulomatous thyroiditis
    • Subacute Granulomatous Thyroiditis
Homo sapiens (human)
DOID:0070134
  • autosomal recessive cutis laxa type IIA
  • Aliases:
    • ARCL2A
Homo sapiens (human)
DOID:4648
  • familial retinoblastoma
  • Aliases:
    • Hereditary Retinoblastoma
Homo sapiens (human)
DOID:0060222
  • Scheie syndrome
  • Aliases:
    • mucopolysaccharidosis type 1S
    • mucopolysaccharidosis type IS
    • mucopolysaccharidosis type V
Homo sapiens (human)
DOID:0050557
  • congenital muscular dystrophy
Homo sapiens (human)
DOID:0060326
  • myelomeningocele
Homo sapiens (human)

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Last updated: August 19, 2024