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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 4326 - 4350 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:5082
  • liver cirrhosis
  • Aliases:
    • Cirrhosis
    • cirrhosis of liver
Xenopus laevis (African clawed frog)
DOID:0050430
  • multiple endocrine neoplasia type 2A
  • Aliases:
    • MEN2A
    • Sipple syndrome
    • multiple endocrine neoplasia II
Mus musculus (house mouse)
DOID:409
  • liver disease
  • Aliases:
    • disorder of liver
    • hepatic disorder
Rattus norvegicus (Norway rat)
DOID:7575
  • pancreatic intraductal papillary-mucinous neoplasm
Mus musculus (house mouse)
DOID:0112347
  • hereditary spastic paraplegia 84
  • Aliases:
    • SPG84
    • spastic paraplegia 84 autosomal recessive
Homo sapiens (human)
DOID:0080560
  • congenital disorder of glycosylation Ih
  • Aliases:
    • congenital disorder of glycosylation 1h
Caenorhabditis elegans
DOID:0060319
  • cardiac arrest
  • Aliases:
    • cardiopulmonary arrest
    • circulatory arrest
Rattus norvegicus (Norway rat)
DOID:4947
  • cholangiocarcinoma
  • Aliases:
    • adult primary Cholangiocarcinoma
    • adult primary cholangiocellular carcinoma
    • cholangiosarcoma
Mus musculus (house mouse)
DOID:8552
  • chronic myeloid leukemia
  • Aliases:
    • CML
    • CML - chronic Myelogenous Leukemia
    • Myeloid Leukemia, chronic
    • chronic granulocytic leukaemia
    • chronic granulocytic leukemia
    • chronic myelogenous leukaemia
    • chronic myelogenous leukemia
    • chronic myeloid leukaemia
Xenopus laevis (African clawed frog)
DOID:885
  • fascioliasis
  • Aliases:
    • Fasciola hepatica infection
    • Infection by Fasciola
    • Liver flukes
    • Sheep liver fluke infection
Rattus norvegicus (Norway rat)
DOID:1712
  • aortic valve stenosis
  • Aliases:
    • Aortic stenosis
    • Rheumatic aortic stenosis
    • rheumatic aortic valve stenosis
Caenorhabditis elegans
DOID:0070296
  • primary autosomal recessive microcephaly
  • Aliases:
    • MCPH
Homo sapiens (human)
DOID:0110459
  • dilated cardiomyopathy 1FF
  • Aliases:
    • CMD1FF
Rattus norvegicus (Norway rat)
DOID:0080000
  • muscular disease
Rattus norvegicus (Norway rat)
DOID:0110423
  • dilated cardiomyopathy 1C
  • Aliases:
    • CMDC1
    • dilated cardiomyopathy 1C with or without left ventricular noncompaction
Mus musculus (house mouse)
DOID:0060210
  • amyotrophic lateral sclerosis type 19
  • Aliases:
    • ALS19
    • amyotrophic lateral sclerosis 19
Homo sapiens (human)
DOID:3910
  • lung adenocarcinoma
  • Aliases:
    • bronchogenic lung adenocarcinoma
    • nonsmall cell adenocarcinoma
Xenopus laevis (African clawed frog)
DOID:8866
  • actinic keratosis
  • Aliases:
    • SK - Solar keratosis
    • Senile hyperkeratosis
    • Solar keratosis
    • actinic (Solar) Keratosis
Homo sapiens (human)
DOID:0070298
  • multiple epiphyseal dysplasia 2
  • Aliases:
    • EDM2
Homo sapiens (human)
DOID:13603
  • obstructive jaundice
  • Aliases:
    • Cholestatic Jaundice
    • Cholestatic jaundice syndrome
    • Obstructive hyperbilirubinemia
Mus musculus (house mouse)
DOID:3907
  • lung squamous cell carcinoma
  • Aliases:
    • Epidermoid cell carcinoma of the lung
Saccharomyces cerevisiae S288C
DOID:3498
  • pancreatic ductal adenocarcinoma
  • Aliases:
    • ductal adenocarcinoma of the pancreas
Rattus norvegicus (Norway rat)
DOID:10923
  • sickle cell anemia
  • Aliases:
    • Hb SC disease
    • Hb-S/Hb-C disease
    • Hb-SS disease without crisis
    • Hemoglobin S disease without crisis
    • Sickle-cell/Hb-C disease without crisis
    • drepanocytosis
    • haemoglobin SC disease
    • hemoglobin SC disease
    • sickle cell anaemia
Danio rerio (zebrafish)
DOID:0112359
  • congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay
  • Aliases:
    • CAKUTHED
Homo sapiens (human)
DOID:0111944
  • immunodeficiency 31B
  • Aliases:
    • IMD31B
    • autosomal recessive STAT1 deficiency
    • autosomal recessive immunodeficiency 31B, mycobacterial and viral infections
    • predisposition to severe viral infection due to STAT1 deficiency
    • susceptibility to viral and mycobacterial infections due to STAT1 deficiency
Homo sapiens (human)
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Last updated: December 9, 2024