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 2326 - 2350 of 4621 in total
Disease ID Disease Name ▼ Gene Symbol Gene ID Organism
DOID:0090065
  • familial cold autoinflammatory syndrome 4
Homo sapiens (human)
DOID:0090064
  • familial cold autoinflammatory syndrome 3
Homo sapiens (human)
DOID:0090062
  • familial cold autoinflammatory syndrome 1
Homo sapiens (human)
DOID:0111677
  • familial benign fleck retina
  • Aliases:
    • FRFB
Homo sapiens (human)
DOID:0050650
  • familial atrial fibrillation
  • Aliases:
    • ATFB
Homo sapiens (human)
DOID:0111418
  • familial apolipoprotein C-II deficiency
  • Aliases:
    • C-II anapolipoproteinemia
    • familial APOC2 deficiency
    • familial apoC-II deficiency
    • hyperlipoproteinemia, type 1b
    • hyperlipoproteinemia, type Ib
Homo sapiens (human)
DOID:0111421
  • familial apolipoprotein A5 deficiency
  • Aliases:
    • familial APOA5 deficiency
    • familial apolipoprotein A-V deficiency
Homo sapiens (human)
DOID:0111691
  • familial adult myoclonic epilepsy 5
  • Aliases:
    • FAME5
    • FCMTE5
    • familial cortical myoclonic tremor and epilepsy 5
Homo sapiens (human)
DOID:0050424
  • familial adenomatous polyposis
  • Aliases:
    • adenomatous polyposis of the colon
Homo sapiens (human)
DOID:0080411
  • familial adenomatous polyposis 3
Homo sapiens (human)
DOID:0080410
  • familial adenomatous polyposis 2
  • Aliases:
    • MUTYH-associated polyposis
    • MUTYH-related attenuated FAP
    • MUTYH-related attenuated familial adenomatous polyposis
    • MUTYH-related attenuated familial polyposis coli
Homo sapiens (human)
DOID:0080409
  • familial adenomatous polyposis 1
Homo sapiens (human)
DOID:0111420
  • familial GPIHBP1 deficiency
  • Aliases:
    • familial glycosylphosphatidylinositol-anchored high density lipoprotein-binding protein 1 deficiency
    • hyperlipoproteinemia type 1D
    • hyperlipoproteinemia type ID
Homo sapiens (human)
DOID:1963
  • fallopian tube carcinoma
  • Aliases:
    • cancer of the fallopian tube
    • carcinoma of fallopian tube
    • fallopian tube Ca
Homo sapiens (human)
DOID:1964
  • fallopian tube cancer
  • Aliases:
    • fallopian tube neoplasm
    • malignant neoplasm of uterine tube
    • malignant tumor of fallopian tube
    • malignant tumour of fallopian tube
    • neoplasm of fallopian tube
    • tumor of the fallopian tube
    • tumor, fallopian tube, malignant
Homo sapiens (human)
DOID:2211
  • factor XIII deficiency
  • Aliases:
    • Factor XIII deficiency disease
    • Hereditary factor XIII deficiency disease
    • deficiency, Laki-Lorand factor
Homo sapiens (human)
DOID:2231
  • factor XII deficiency
  • Aliases:
    • Factor XII deficiency disease
    • Hageman Factor deficiency
    • deficiency, Hageman
Homo sapiens (human)
DOID:12134
  • factor VIII deficiency
  • Aliases:
    • Congenital factor VIII disorder
    • Hemophilia A
    • Subhemophilia
    • classic hemophilia A
Homo sapiens (human)
DOID:2215
  • factor VII deficiency
  • Aliases:
    • deficiency, stable
Homo sapiens (human)
DOID:2216
  • factor V deficiency
  • Aliases:
    • Hereditary hypoproaccelerinaemia
    • Labile factor deficiency
    • Proaccelerin deficiency
    • deficiency, labile
Homo sapiens (human)
DOID:11727
  • facioscapulohumeral muscular dystrophy
  • Aliases:
    • Landouzy Dejerine muscular dystrophy
    • Landouzy-Dejerine muscular dystrophy
    • Muscular dystrophy, Landouzy-Dejerine
Homo sapiens (human)
DOID:0111192
  • facioscapulohumeral muscular dystrophy 1
  • Aliases:
    • FSHD1
    • facioscapulohumeral muscular dystrophy type 1
    • facioscapulohumeral muscular dystrophy type 1A
Homo sapiens (human)
DOID:13934
  • facial paralysis
  • Aliases:
    • Facial Palsy
Homo sapiens (human)
DOID:1756
  • facial nerve disease
Homo sapiens (human)
DOID:1757
  • facial hemiatrophy
  • Aliases:
    • PARRY-ROMBERG SYNDROME
Homo sapiens (human)

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Last updated: August 19, 2024