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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 3626 - 3650 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Organism Source
DOID:0111150
  • autosomal dominant isolated ectopia lentis 1
  • Aliases:
    • ECTOL1
Mus musculus (house mouse)
DOID:0111561
  • stiff skin syndrome
  • Aliases:
    • SSKS
Mus musculus (house mouse)
DOID:0060218
  • CREST syndrome
Mus musculus (house mouse)
DOID:0111595
  • congenital contractural arachnodactyly
  • Aliases:
    • Beals syndrome
    • Beals-Hecht syndrome
    • CCA
    • arachnodactyly, contractural Beals type
    • contractures, multiple with arachnodactyly
    • distal arthrogryposis type 9
    • ear anomalies-contractures-dysplasia of bone with kyphoscoliosis
Mus musculus (house mouse)
DOID:5204
  • fructose-1,6-bisphosphatase deficiency
  • Aliases:
    • fructose 1 phosphate aldolase deficiency
    • fructose-1,6-diphosphatase deficiency
Mus musculus (house mouse)
DOID:12177
  • common variable immunodeficiency
  • Aliases:
    • CVID
    • acquired agammaglobulinemia
    • acquired hypogammaglobulinemia
    • common variable agammaglobulinemia
    • sporadic hypogammaglobulinemia
Mus musculus (house mouse)
DOID:0080179
  • haemophilus meningitis
Mus musculus (house mouse)
DOID:1098
  • fetal erythroblastosis
  • Aliases:
    • EF - Erythroblastosis foetalis
    • Haemolytic disease due to rhesus isoimmunisation
    • erythroblastosis fetalis
    • rhesus isoimmunisation of the newborn
Mus musculus (house mouse)
DOID:0060604
  • ankyloglossia
  • Aliases:
    • tongue-tie
Mus musculus (house mouse)
DOID:0112313
  • brain small vessel disease
Mus musculus (house mouse)
DOID:484
  • vascular hemostatic disease
Mus musculus (house mouse)
DOID:0050636
  • familial visceral amyloidosis
  • Aliases:
    • AMYLOIDOSIS, FAMILIAL RENAL
    • German type amyloidosis
    • OSTERTAG TYPE AMYLOIDOSIS
    • systemic nonneuropathic amyloidosis
Mus musculus (house mouse)
DOID:0080425
  • developmental and epileptic encephalopathy 47
  • Aliases:
    • DEE47
    • early infantile epileptic encephalopathy 47
Mus musculus (house mouse)
DOID:0050331
  • lacrimoauriculodentodigital syndrome 1
  • Aliases:
    • LEVY-HOLLISTER SYNDROME
    • Lacrimo-auriculo-dento-digital syndrome 1
Mus musculus (house mouse)
DOID:0081372
  • lacrimoauriculodentodigital syndrome 3
  • Aliases:
    • Lacrimo-auriculo-dento-digital syndrome 3
Mus musculus (house mouse)
DOID:0111549
  • aplasia of lacrimal and salivary glands
  • Aliases:
    • ALSG
    • congenital absence of lacrimal puncta and salivary glands
Mus musculus (house mouse)
DOID:0090082
  • hypogonadotropic hypogonadism 20 with or without anosmia
Mus musculus (house mouse)
DOID:0111566
  • familial isolated trichomegaly
  • Aliases:
    • TCMGLY
    • long eyelashes
Mus musculus (house mouse)
DOID:3594
  • choriocarcinoma
  • Aliases:
    • Chorioepithelioma
Mus musculus (house mouse)
DOID:0090086
  • hypogonadotropic hypogonadism 6 with or without anosmia
Mus musculus (house mouse)
DOID:0050794
  • multiple synostoses syndrome
Mus musculus (house mouse)
DOID:263
  • kidney cancer
  • Aliases:
    • malignant neoplasm of kidney except pelvis
    • malignant tumour of kidney
    • renal cancer
Mus musculus (house mouse)
DOID:4769
  • pleuropulmonary blastoma
Mus musculus (house mouse)
DOID:0081319
  • multiple synostoses syndrome 3
Mus musculus (house mouse)
DOID:0111337
  • Jackson-Weiss syndrome
  • Aliases:
    • JWS
    • craniosynostosis-midfacial hypoplasia-foot abnormalities syndrome
Mus musculus (house mouse)
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: December 9, 2024