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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 October 9, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 10351 - 10375 of 15957 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism Source
DOID:2962
  • Cockayne syndrome
  • Aliases:
    • Neill-Dingwall syndrome
Homo sapiens (human)
DOID:0060210
  • amyotrophic lateral sclerosis type 19
  • Aliases:
    • ALS19
    • amyotrophic lateral sclerosis 19
Homo sapiens (human)
DOID:4306
  • radiculopathy
  • Aliases:
    • pinched nerve
Homo sapiens (human)
DOID:0060560
  • lethal congenital contracture syndrome 2
  • Aliases:
    • LCCS2
    • multiple contracture syndrome, Israeli-Bedouin type
Homo sapiens (human)
DOID:0080679
  • neuronal intestinal dysplasia type A
Homo sapiens (human)
DOID:3443
  • mammary Paget's disease
  • Aliases:
    • Paget cell neoplasm
    • Paget's disease
    • Paget's disease of the breast
    • mammary Paget disease
Homo sapiens (human)
DOID:10376
  • amblyopia
  • Aliases:
    • lazy eye
Homo sapiens (human)
DOID:9415
  • allergic asthma
  • Aliases:
    • extrinsic asthma with acute exacerbation
    • extrinsic asthma with status asthmaticus
Homo sapiens (human)
DOID:0080261
  • autosomal recessive nonsyndromic deafness 106
Homo sapiens (human)
DOID:0110463
  • autosomal recessive nonsyndromic deafness 102
  • Aliases:
    • DFNB102
    • autosomal recessive deafness 102
Homo sapiens (human)
DOID:0070398
  • hypomyelinating leukodystrophy 15
  • Aliases:
    • HLD15
Homo sapiens (human)
DOID:0060652
  • familial erythrocytosis 1
  • Aliases:
    • ECYT1
    • autosomal dominant benign erythrocytosis
    • primary familial and congenital polycythemia
Homo sapiens (human)
DOID:0080290
  • familial erythrocytosis 5
  • Aliases:
    • ECYT5
Homo sapiens (human)
DOID:891
  • progressive myoclonus epilepsy
  • Aliases:
    • PME
    • progressive myoclonic epilepsy
Homo sapiens (human)
DOID:3534
  • Lafora disease
  • Aliases:
    • Lafora Progressive Myoclonic Epilepsy
    • Lafora's disease
    • MYOCLONIC EPILEPSY OF LAFORA
Homo sapiens (human)
DOID:0081030
  • central conducting lymphatic anomaly
  • Aliases:
    • lymphatic malformation-7
Homo sapiens (human)
DOID:75
  • lymphatic system disease
  • Aliases:
    • Lymphangiopathy
    • Lymphatic disease
    • disease of lympoid system
    • disorder of lymph node and lymphatics
    • disorder of lymphatic system
    • disorder of lymphoid system
    • lymphatic disorder
    • lympoid system disease
Homo sapiens (human)
DOID:0110229
  • cataract 6 multiple types
  • Aliases:
    • CTRCT6
Homo sapiens (human)
DOID:0060356
  • Vici syndrome
  • Aliases:
    • immunodeficiency with cleft lip/palate, cataract, hypopigmentation, and absent corpus callosum
Homo sapiens (human)
DOID:0060776
  • congenital diarrhea 5 with tufting enteropathy
  • Aliases:
    • DIAR5
    • congenital diarrhoea 5 with tufting enteropathy
    • congenital familial intractable diarrhea with epithelial or epithelium abnormalities
    • congenital familial intractable diarrhoea with epithelial or epithelium abnormalities
    • congenital tufting enteropathy
    • tufting enteropathy
Homo sapiens (human)
DOID:0070270
  • hereditary nonpolyposis colorectal cancer type 8
  • Aliases:
    • HNPCC8
Homo sapiens (human)
DOID:0110920
  • hereditary spherocytosis type 5
  • Aliases:
    • HS5
    • SPH5
    • hereditary spherocytosis 5
Homo sapiens (human)
DOID:3565
  • meningioma
  • Aliases:
    • meningeal neoplasm
    • meningothelial cell tumor
    • neoplasm of the meninges
    • primary Meningeal tumor
Homo sapiens (human)
DOID:0070041
  • autosomal dominant intellectual developmental disorder 11
  • Aliases:
    • MRD11
    • autosomal dominant mental retardation 11
    • autosomal dominant non-syndromic intellectual disability 11
Homo sapiens (human)
DOID:2373
  • hereditary elliptocytosis
  • Aliases:
    • Congenital elliptocytosis
    • ovalocytosis
Homo sapiens (human)
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Last updated: December 9, 2024