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 5001 - 5025 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲
DOID:0110548
  • autosomal dominant nonsyndromic deafness 17
  • Aliases:
    • DFNA17
    • autosomal dominant deafness 17
Homo sapiens (human)
DOID:2154
  • nephroblastoma
  • Aliases:
    • adult nephroblastoma
Homo sapiens (human)
DOID:10017
  • multiple endocrine neoplasia type 1
  • Aliases:
    • MEN type I
    • Wermer syndrome
    • Wermer's syndrome
Homo sapiens (human)
DOID:520
  • aortic disease
  • Aliases:
    • aortic disorder
    • disorder of the aorta
Homo sapiens (human)
DOID:10908
  • hydrocephalus
  • Aliases:
    • hydrocephalus, X-linked
    • hydrocephalus, nonsyndromic, autosomal recessive
Homo sapiens (human)
DOID:574
  • peripheral nervous system disease
Homo sapiens (human)
DOID:3030
  • mucinous adenocarcinoma
  • Aliases:
    • Mucin-Secreting adenocarcinoma
    • Mucin-Secreting carcinoma
    • Mucous carcinoma
    • Pseudomyxoma peritonei with unknown primary site
    • mucin-producing adenocarcinoma
Homo sapiens (human)
DOID:0060700
  • familial hypocalciuric hypercalcemia 1
  • Aliases:
    • FHH type 1
    • HHC1
    • familial benign hypercalcemia 1
    • familial hypocalciuric hypercalcemia type I
    • hypocalciuric hypercalcemia type I
Homo sapiens (human)
DOID:11123
  • Henoch-Schoenlein purpura
  • Aliases:
    • Allergic purpura
    • Autoimmune purpura
    • Henoch-Sch?nlein purpura
    • Henoch-Sch@nlein purpura
    • Henoch-Scholein purpura
    • Henoch-Schonlein Purpura
    • Purpura, autoimmune
Homo sapiens (human)
DOID:0050848
  • obstructive sleep apnea
  • Aliases:
    • obstructive sleep apnea syndrome
Homo sapiens (human)
DOID:4914
  • esophagus adenocarcinoma
  • Aliases:
    • Oesophageal adenocarcinoma
Homo sapiens (human)
DOID:8947
  • diabetic retinopathy
  • Aliases:
    • Retinal abnormality - diabetes-related
Homo sapiens (human)
DOID:0110771
  • hereditary spastic paraplegia 18
  • Aliases:
    • IDMDC
    • SPG18
    • autosomal recessive spastic paraplegia 18
    • autosomal recessive spastic paraplegia type 18
    • intellectual disability, motor dysfunction and joint contractures
Homo sapiens (human)
DOID:0110809
  • hereditary spastic paraplegia 57
  • Aliases:
    • SPG57
    • autosomal recessive spastic paraplegia 57
    • autosomal recessive spastic paraplegia type 57
Homo sapiens (human)
DOID:1324
  • lung cancer
Homo sapiens (human)
DOID:0060676
  • catecholaminergic polymorphic ventricular tachycardia 2
  • Aliases:
    • CVPT2
Homo sapiens (human)
DOID:1407
  • anterior uveitis
Homo sapiens (human)
DOID:6067
  • ovarian mucinous neoplasm
  • Aliases:
    • Ovarian mucinous tumor
    • malignant ovarian mucinous neoplasm
    • mucinous tumor of Ovary
Homo sapiens (human)
DOID:1059
  • intellectual disability
Homo sapiens (human)
DOID:0080411
  • familial adenomatous polyposis 3
Homo sapiens (human)
DOID:3165
  • skin benign neoplasm
  • Aliases:
    • neoplasm of skin
    • neoplasm of skin by site
    • skin neoplasm
    • tumor of the skin
Homo sapiens (human)
DOID:12506
  • Bell's palsy
  • Aliases:
    • Bell palsy
    • Bell's (facial) palsy
Homo sapiens (human)
DOID:4001
  • ovarian carcinoma
Homo sapiens (human)
DOID:0110810
  • hereditary spastic paraplegia 5A
  • Aliases:
    • SPG5A
    • autosomal recessive spastic paraplegia 5A
    • autosomal recessive spastic paraplegia type 5A
Homo sapiens (human)
DOID:1664
  • pineoblastoma
  • Aliases:
    • Pineal PNET
Homo sapiens (human)

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Last updated: August 19, 2024