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 2776 - 2800 of 4621 in total
Disease ID Disease Name ▲ Gene Symbol Gene ID Organism
DOID:9955
  • hypoplastic left heart syndrome
Homo sapiens (human)
DOID:10892
  • hypospadias
  • Aliases:
    • familial hypospadias
Homo sapiens (human)
DOID:1931
  • hypothalamic disease
Homo sapiens (human)
DOID:1459
  • hypothyroidism
  • Aliases:
    • Thyroid deficiency
    • Thyroid insufficiency
Homo sapiens (human)
DOID:0060858
  • hypotonia-cystinuria syndrome
  • Aliases:
    • cystinuria with mitochondrial disease
Homo sapiens (human)
DOID:0110698
  • hypotrichosis 1
  • Aliases:
    • Hhs
    • Hts
    • Hypt1
    • hereditary generalized hypotrichosis simplex
Homo sapiens (human)
DOID:0080582
  • hypotrichosis 14
Homo sapiens (human)
DOID:0110704
  • hypotrichosis 7
  • Aliases:
    • Hypt7
    • Lah2
    • hypotrichosis, localized, autosomal recessive 2
    • total Mari type hypotrichosis,
Homo sapiens (human)
DOID:4535
  • hypotrichosis
Homo sapiens (human)
DOID:1702
  • ichthyosis vulgaris
  • Aliases:
    • Dominant congenital ichthyosiform erythroderma
Homo sapiens (human)
DOID:1697
  • ichthyosis
  • Aliases:
    • ichthyoses
    • non-syndromic ichthyosis
Homo sapiens (human)
DOID:0111313
  • idiopathic generalized epilepsy 12
  • Aliases:
    • EIG12
Homo sapiens (human)
DOID:1827
  • idiopathic generalized epilepsy
  • Aliases:
    • Generalised epilepsy
Homo sapiens (human)
DOID:2797
  • idiopathic interstitial pneumonia
  • Aliases:
    • Diffuse idiopathic pulmonary fibrosis
    • Idiopathic fibrosing alveolitis
Homo sapiens (human)
DOID:12559
  • idiopathic juvenile osteoporosis
  • Aliases:
    • Idiopathic osteoporosis
    • juvenile osteoporosis
Homo sapiens (human)
DOID:0050156
  • idiopathic pulmonary fibrosis
  • Aliases:
    • FIBROCYSTIC PULMONARY DYSPLASIA
    • IDIOPATHIC PULMONARY FIBROSIS, FAMILIAL
    • cryptogenic fibrosing alveolitis
Homo sapiens (human)
DOID:0060250
  • idiopathic scoliosis
Homo sapiens (human)
DOID:0060189
  • ileitis
  • Aliases:
    • Crohn's ileitis
Homo sapiens (human)
DOID:0060190
  • ileocolitis
Homo sapiens (human)
DOID:8440
  • ileus
  • Aliases:
    • Ileus of intestine
Homo sapiens (human)
DOID:0090110
  • immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome
  • Aliases:
    • Autoimmune enteropathy type 1
    • DMSD
    • IDDM-secretory diarrhea syndrome
    • IPEX
    • X-linked autoimmunity-allergic dysregulation syndrome
    • XLAAD
    • XPID
    • autoimmunity-immunodeficiency syndrome, X-linked
    • diabetes mellitus, congenital insulin-dependent, with fatal secretory diarrhea
    • diarrhea, polyendocrinopathy, fatal infection syndrome, X-linked
    • immunodeficiency, polyendocrinopathy, and enteropathy, X-linked
    • immunodysregulation, polyendocrinopathy, and enteropathy, X-Linked
Homo sapiens (human)
DOID:2914
  • immune system disease
Homo sapiens (human)
DOID:4784
  • immune-complex glomerulonephritis
  • Aliases:
    • Immune Complex Glomerulonephritis
Homo sapiens (human)
DOID:0111936
  • immunodeficiency 14
  • Aliases:
    • APDS
    • IMD14
    • PASLI disease
    • activated PI3K-delta syndrome
    • senescent T-cells-lymphadenopathy-immunodeficiency syndrome due to p110delta-activating mutation
Homo sapiens (human)
DOID:0111953
  • immunodeficiency 23
  • Aliases:
    • CID due to PGM3 deficiency
    • IMD23
    • PGM3-CDG
    • PGM3-related congenital disorder of glycosylation
    • combined immunodeficiency due to PGM3 deficiency
Homo sapiens (human)

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Supported by JST NBDC Grant Number JPMJND2204

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Last updated: August 19, 2024