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 9426 - 9450 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Organism Source
DOID:0060646
  • congenital chylothorax
Homo sapiens (human)
DOID:0080135
  • multiple mitochondrial dysfunctions syndrome 3
  • Aliases:
    • IBA57 deficiency
Homo sapiens (human)
DOID:0110819
  • hereditary spastic paraplegia 74
  • Aliases:
    • SPG74
    • autosomal recessive spastic paraplegia 74
Homo sapiens (human)
DOID:0112337
  • spermatogenic failure 55
  • Aliases:
    • SPGF55
Homo sapiens (human)
DOID:2320
  • obstructive lung disease
  • Aliases:
    • respiratory airway obstruction
Homo sapiens (human)
DOID:10113
  • trypanosomiasis
Homo sapiens (human)
DOID:13208
  • background diabetic retinopathy
  • Aliases:
    • Non proliferative diabetic retinopathy
    • Non-Proliferative Diabetic Retinopathy
Homo sapiens (human)
DOID:583
  • hemolytic anemia
  • Aliases:
    • ANEMIA HEMOLYTIC
Homo sapiens (human)
DOID:8283
  • peritonitis
  • Aliases:
    • Retractile mesenteritis
    • acute generalized peritonitis
    • primary bacterial peritonitis
    • sclerosing mesenteritis
Homo sapiens (human)
DOID:0110658
  • congenital myasthenic syndrome 15
  • Aliases:
    • CMS15
    • congenital myasthenic syndrome 15 without tubular aggregates
Homo sapiens (human)
DOID:0111892
  • Diamond-Blackfan anemia 11
  • Aliases:
    • DBA11
    • RPL26-related Diamond-Blackfan anemia
Mus musculus (house mouse)
DOID:0111927
  • spermatogenic failure 37
  • Aliases:
    • SPGF37
Homo sapiens (human)
DOID:12712
  • nephronophthisis
  • Aliases:
    • medullary cystic disease
    • medullary cystic kidney
Homo sapiens (human)
DOID:2562
  • suppurative periapical periodontitis
  • Aliases:
    • Apical abscess
    • Dentoalveolar abscess
    • Periapical abscess
    • Suppurative apical periodontitis
Homo sapiens (human)
DOID:0080625
  • severe congenital neutropenia 1
Homo sapiens (human)
DOID:5339
  • cyclic hematopoiesis
  • Aliases:
    • Cyclic neutropenia
    • Cyclical neutropenia
    • Neutropenia, periodic
    • cyclic agranulocytosis
Homo sapiens (human)
DOID:2224
  • essential thrombocythemia
  • Aliases:
    • Essential thrombocythaemia
    • familial thrombocytosis
    • hemorrhagic thrombocythemia
    • hereditary thrombocythemia
    • primary Thrombocytosis
Homo sapiens (human)
DOID:0080178
  • mucositis
Homo sapiens (human)
DOID:8997
  • polycythemia vera
  • Aliases:
    • Osler-Vaquez syndrome
    • Polycythaemia rubra vera
    • Proliferative polycythaemia
    • chronic erythremia
Homo sapiens (human)
DOID:0110414
  • retinitis pigmentosa 3
  • Aliases:
    • RP3
Mus musculus (house mouse)
DOID:0112157
  • X-linked atrophic macular degeneration
Mus musculus (house mouse)
DOID:0112124
  • X-linked retinitis pigmentosa and sinorespiratory infections
  • Aliases:
    • primary ciliary dyskinesia-retinitis pigmentosa syndrome
Mus musculus (house mouse)
DOID:0111008
  • X-linked cone-rod dystrophy 1
  • Aliases:
    • COD1
    • CORDX1
    • X-linked cone dystrophy 1
Mus musculus (house mouse)
DOID:3721
  • plasmacytoma
  • Aliases:
    • Myeloma - solitary
    • Myeloma, solitary
    • Solitary myeloma
    • Solitary plasmacytoma
Mus musculus (house mouse)
DOID:9410
  • panhypopituitarism
  • Aliases:
    • Simmond's disease
    • Simmonds' disease
    • combined pituitary hormone deficiency
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