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 2876 - 2900 of 4621 in total
Disease ID Disease Name ▲ Gene Symbol Gene ID Organism
DOID:8446
  • intussusception
  • Aliases:
    • Intussusception of intestine
    • Invagination of intestine or colon
Homo sapiens (human)
DOID:0050073
  • invasive aspergillosis
Homo sapiens (human)
DOID:3008
  • invasive ductal carcinoma
  • Aliases:
    • Infiltrating ductal carcinoma of breast
    • Invasive ductal carcinoma, NST
    • ductal adenocarcinoma
Homo sapiens (human)
DOID:3457
  • invasive lobular carcinoma
  • Aliases:
    • Lobular carcinoma
    • Lobular carcinoma of breast
    • Lobular carcinoma of the breast
Homo sapiens (human)
DOID:3283
  • invasive malignant thymoma
  • Aliases:
    • Infiltrating Thymoma
    • Thymoma malignant Invasive
Homo sapiens (human)
DOID:6945
  • inverted follicular keratosis
  • Aliases:
    • Inverted folicular keratosis
Homo sapiens (human)
DOID:3179
  • inverted papilloma
  • Aliases:
    • Inverted papilloma, squamous cell
Homo sapiens (human)
DOID:9383
  • iridocyclitis
  • Aliases:
    • primary iridocyclitis
Homo sapiens (human)
DOID:240
  • iris disease
Homo sapiens (human)
DOID:11758
  • iron deficiency anemia
Homo sapiens (human)
DOID:2351
  • iron metabolism disease
  • Aliases:
    • disorder of iron metabolism
    • iron disorder
Homo sapiens (human)
DOID:9778
  • irritable bowel syndrome
  • Aliases:
    • IBD
    • Irritable colon
Homo sapiens (human)
DOID:2772
  • irritant dermatitis
  • Aliases:
    • irritant contact dermatitis
    • primary irritant dermatitis
Homo sapiens (human)
DOID:326
  • ischemia
Homo sapiens (human)
DOID:0060181
  • ischemic colitis
Homo sapiens (human)
DOID:0111382
  • ischiocoxopodopatellar syndrome
  • Aliases:
    • SPS
    • Scott-Taor syndrome
    • congenital coxa vara, patella aplasia and tarsal synostosis
    • coxo-podo-patellar syndrome
    • coxopodipatellar syndrome
    • ischiocoxopodopatellar syndrome with or without pulmonary arterial hypertension
    • ischiopatellar dysplasia
    • patella aplasia, coxa vara, and tarsal synostosis
    • small patella syndrome
Homo sapiens (human)
DOID:1799
  • islet cell tumor
  • Aliases:
    • Islet cell neoplasm
    • endocrine pancreas cancer
    • islet cell tumour
    • malignant pancreatic Endocrine tumor
    • malignant pancreatic Endocrine tumour
    • malignant tumor of endocrine pancreas
    • malignant tumour of endocrine pancreas
    • pancreatic Endocrine neoplasm
Homo sapiens (human)
DOID:0110213
  • isolated cleft palate
Homo sapiens (human)
DOID:0111148
  • isolated ectopia lentis
  • Aliases:
    • IEL
    • familial ectopia lentis
Homo sapiens (human)
DOID:0111338
  • isolated elevated serum creatine phosphokinase levels
  • Aliases:
    • elevated serum CPK
    • idiopathic hyperCKemia
    • isolated hyperCKemia
Homo sapiens (human)
DOID:0060873
  • isolated growth hormone deficiency type IA
  • Aliases:
    • IGHD IA
    • Illig-type growth hormone deficiency
    • autosomal recessive isolated growth hormone deficiency
    • pituitary dwarfism I
    • primordial dwarfism
    • sexual ateleiotic dwarfism
Homo sapiens (human)
DOID:0060874
  • isolated growth hormone deficiency type IB
  • Aliases:
    • IGHD IB
    • congenital IGHD type IB
    • congenital isolated GH deficiency type IB
    • congenital isolated growth hormone deficiency type IB
    • dwarfism of Sindh
Homo sapiens (human)
DOID:0060872
  • isolated growth hormone deficiency type II
  • Aliases:
    • IGHD II
    • autosomal dominant isolated growth hormone deficiency
    • autosomal dominant pituitary dwarfism due to isolated growth hormone deficiency
    • congenital IGHD type II
    • congenital isolated GH deficiency type II
    • congenital isolated growth hormone deficiency type II
Homo sapiens (human)
DOID:0060875
  • isolated growth hormone deficiency type III
  • Aliases:
    • Fleisher syndrome
    • IGHD III
    • X-linked IGHD
    • X-linked agammaglobulinemia and isolated growth hormone deficiency
    • X-linked hypogammaglobulinemia and isolated growth hormone deficiency
    • X-linked isolated growth hormone deficiency
    • congenital IGHD type III
    • congenital isolated GH deficiency type III
    • congenital isolated growth hormone deficiency type III
    • growth hormone deficiency with hypogammaglobulinemia
Homo sapiens (human)
DOID:0060870
  • isolated growth hormone deficiency
  • Aliases:
    • IGHD
    • congenital IGHD
    • congenital isolated GH deficiency
    • congenital isolated growth hormone deficiency
    • familial isolated growth hormone deficiency
    • non-acquired isolated growth hormone deficiency
Homo sapiens (human)

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Supported by JST NBDC Grant Number JPMJND2204

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Last updated: August 19, 2024