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 2276 - 2300 of 4621 in total
Disease ID Disease Name ▼ Gene Symbol Gene ID Organism
DOID:0111377
  • fetal akinesia deformation sequence syndrome 1
  • Aliases:
    • FADS1
Homo sapiens (human)
DOID:724
  • female stress incontinence
  • Aliases:
    • Stress incontinence - female
    • female urinary stress incontinence
Homo sapiens (human)
DOID:229
  • female reproductive system disease
Homo sapiens (human)
DOID:120
  • female reproductive organ cancer
  • Aliases:
    • female reproductive cancer
    • malignant Gynecologic tumor
    • malignant neoplasm of female genital organ
Homo sapiens (human)
DOID:3001
  • female reproductive endometrioid cancer
  • Aliases:
    • endometrioid neoplasm
    • endometrioid tumor
Homo sapiens (human)
DOID:7843
  • female breast carcinoma
  • Aliases:
    • Mammary carcinoma of female breast
Homo sapiens (human)
DOID:13628
  • favism
Homo sapiens (human)
DOID:0050433
  • fatal familial insomnia
Homo sapiens (human)
DOID:885
  • fascioliasis
  • Aliases:
    • Fasciola hepatica infection
    • Infection by Fasciola
    • Liver flukes
    • Sheep liver fluke infection
Homo sapiens (human)
DOID:9598
  • fasciitis
Homo sapiens (human)
DOID:14453
  • farmer's lung
  • Aliases:
    • Farmers lung
    • farmer lung
Homo sapiens (human)
DOID:6901
  • familiar ovarian carcinoma
Homo sapiens (human)
DOID:0050636
  • familial visceral amyloidosis
  • Aliases:
    • AMYLOIDOSIS, FAMILIAL RENAL
    • German type amyloidosis
    • OSTERTAG TYPE AMYLOIDOSIS
    • systemic nonneuropathic amyloidosis
Homo sapiens (human)
DOID:4648
  • familial retinoblastoma
  • Aliases:
    • Hereditary Retinoblastoma
Homo sapiens (human)
DOID:6163
  • familial renal papillary carcinoma
  • Aliases:
    • Hereditary Papillary renal carcinoma
Homo sapiens (human)
DOID:1029
  • familial periodic paralysis
Homo sapiens (human)
DOID:0050440
  • familial partial lipodystrophy
  • Aliases:
    • Dunnigan Syndrome
    • Koberling-Dunnigan Syndrome
Homo sapiens (human)
DOID:0070202
  • familial partial lipodystrophy type 2
  • Aliases:
    • FPLD2
    • familial lipodystrophy of limbs and lower trunk
    • familial partial lipodystrophy Dunnigan type
    • reverse partial lipodystrophy
Homo sapiens (human)
DOID:2590
  • familial nephrotic syndrome
  • Aliases:
    • Congenital nephrotic syndrome
Homo sapiens (human)
DOID:0111529
  • familial multiple nevi flammei
  • Aliases:
    • CMC
    • congenital capillary malformations
    • familial multiple port-wine stains
Homo sapiens (human)
DOID:4586
  • familial meningioma
Homo sapiens (human)
DOID:6846
  • familial melanoma
Homo sapiens (human)
DOID:0050547
  • familial medullary thyroid carcinoma
  • Aliases:
    • THYROID CARCINOMA, FAMILIAL MEDULLARY
Homo sapiens (human)
DOID:2987
  • familial mediterranean fever
  • Aliases:
    • FMF
    • benign paroxysmal peritonitis
Homo sapiens (human)
DOID:14118
  • familial lipoprotein lipase deficiency
  • Aliases:
    • Fredrickson type I hyperlipoproteinemia
    • Fredrickson type I lipaemia
    • familial LPL deficiency
    • familial hyperlipoproteinemia type I
    • hypercholesterinaemic xanthomatosis
    • hyperchylomicronemia
    • mixed hyperglyceridemia
Homo sapiens (human)

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Supported by JST NBDC Grant Number JPMJND2204

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


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Last updated: August 19, 2024