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 3301 - 3325 of 4621 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼
DOID:13198
  • endemic goiter
  • Aliases:
    • Iodine-deficiency-related endemic goitre
    • simple goitre
Homo sapiens (human)
DOID:4661
  • multiple chemical sensitivity
  • Aliases:
    • 20th century disease
    • chemical AIDS
    • environmental illness
    • idiopathic environmental illness
    • total allergy syndrome
Homo sapiens (human)
DOID:14773
  • cartilage-hair hypoplasia
  • Aliases:
    • CHH
    • McKusick type metaphyseal chondrodysplasia
    • Metaphyseal chondrodysplasia, McKusick type
Homo sapiens (human)
DOID:4798
  • aggressive systemic mastocytosis
  • Aliases:
    • ASM
    • Lymphadenopathic mastocytosis with eosinophilia
Homo sapiens (human)
DOID:12132
  • granulomatosis with polyangiitis
  • Aliases:
    • Necrotizing respiratory granulomatosis
    • Wegener granulomatosis, formerly
Homo sapiens (human)
DOID:9423
  • blepharitis
Homo sapiens (human)
DOID:10808
  • gastric ulcer
  • Aliases:
    • acute gastric ulcer with haemorrhage and perforation
    • acute gastric ulcer with hemorrhage AND with perforation but without obstruction
    • acute gastric ulcer with hemorrhage and obstruction
    • acute gastric ulcer with hemorrhage and perforation
    • acute gastric ulcer with hemorrhage and perforation, with obstruction
    • acute gastric ulcer with hemorrhage and perforation, without mention of obstruction
    • acute gastric ulcer with hemorrhage, with obstruction
    • acute gastric ulcer with hemorrhage, with perforation AND with obstruction
    • acute gastric ulcer with perforation
    • acute gastric ulcer with perforation AND obstruction
    • acute gastric ulcer with perforation, with obstruction
    • acute gastric ulcer without hemorrhage and without perforation
    • acute gastric ulcer without hemorrhage, without perforation AND without obstruction
    • acute gastric ulcer without mention of hemorrhage or perforation, without mention of obstruction
    • bleeding acute gastric ulcer
    • chronic gastric ulcer without hemorrhage AND without perforation
    • chronic gastric ulcer without hemorrhage AND without perforation but with obstruction
    • chronic gastric ulcer without mention of hemorrhage or perforation, with obstruction
Homo sapiens (human)
DOID:2187
  • amelogenesis imperfecta
Homo sapiens (human)
DOID:0080326
  • familial hypertrophic cardiomyopathy
Homo sapiens (human)
DOID:14687
  • diastrophic dysplasia
Homo sapiens (human)
DOID:2152
  • ovary epithelial cancer
  • Aliases:
    • Ovarian Surface epithelial-Stromal tumor
Homo sapiens (human)
DOID:0070124
  • congenital nongoitrous hypothyroidism 2
  • Aliases:
    • CHNG2
    • congenital hypothyroidism due to thyroid dysgenesis or hypoplasia
Homo sapiens (human)
DOID:14177
  • congenital hypogammaglobulinemia
  • Aliases:
    • Congenital hypogammaglobulinaemia
Homo sapiens (human)
DOID:0110726
  • neuronal ceroid lipofuscinosis 2
  • Aliases:
    • CLN2
    • neuronal ceroid lipofuscinosis 2 variable age at onset
Homo sapiens (human)
DOID:0110251
  • cataract 15 multiple types
  • Aliases:
    • CTRCT15
Homo sapiens (human)
DOID:0110236
  • cataract 39 multiple types
  • Aliases:
    • CTRCT39
    • autosomal dominant cataract 39 multiple types
Homo sapiens (human)
DOID:13364
  • obsolete chronobiology disease
Homo sapiens (human)
DOID:318
  • progressive muscular atrophy
  • Aliases:
    • Pure progressive muscular atrophy
    • progressive spinal muscular atrophy
Homo sapiens (human)
DOID:4411
  • hepatitis E
Homo sapiens (human)
DOID:0112022
  • non-syndromic X-linked intellectual disability 21
  • Aliases:
    • MRX21
    • MRX34
    • X-linked mental retardation 21
    • X-linked mental retardation 21/34
    • X-linked mental retardation 34
Homo sapiens (human)
DOID:0110230
  • cataract 34 multiple types
  • Aliases:
    • CATC3
    • CTRCT34
    • autosomal recessive congenital cataract 3
    • cataract 34 multiple types with or without microcornea
Homo sapiens (human)
DOID:6376
  • hypersplenism
  • Aliases:
    • hypersplenia
Homo sapiens (human)
DOID:2226
  • myeloproliferative neoplasm
  • Aliases:
    • CMPD
    • CMPD, U
    • chronic myeloproliferative disease
Homo sapiens (human)
DOID:1271
  • capillary disease
  • Aliases:
    • disease of capillaries
Homo sapiens (human)
DOID:0080140
  • multiple congenital anomalies-hypotonia-seizures syndrome 3
  • Aliases:
    • M syndrome
    • light fixation seizure syndrome
Homo sapiens (human)

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Last updated: August 19, 2024