GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB) and Alliance of Genome Resources is integrated into one list.

Source Last Updated
Alliance of Genome Resources October 9, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 6851 - 6875 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Organism Source
DOID:11695
  • portal vein thrombosis
Homo sapiens (human)
DOID:8536
  • herpes zoster
  • Aliases:
    • Shingles
    • herpes zona
Homo sapiens (human)
DOID:2297
  • leptospirosis
  • Aliases:
    • Fort Bragg fever
    • Leptospirosis icterohaemorrhagica
    • Rat Catcher's Yellows
    • Weil's disease
    • nanukayami fever
    • spirochetal jaundice
Homo sapiens (human)
DOID:8337
  • appendicitis
  • Aliases:
    • acute appendicitis
    • acute appendicitis with generalized peritonitis
    • acute appendicitis with peritoneal abscess
Homo sapiens (human)
DOID:0081215
  • autosomal recessive intellectual developmental disorder 52
Mus musculus (house mouse)
DOID:10588
  • adrenoleukodystrophy
  • Aliases:
    • ALD
    • Bronze Schilder disease
    • Encephalitis periaxialis concentrica
    • Encephalitis periaxialis, Schilder's
    • Siemerling-Creutzfeldt Disease
    • X-linked adrenoleukodystrophy
    • diffuse sclerosis
    • sudanophilic cerebral sclerosis
Homo sapiens (human)
DOID:0060496
  • respiratory allergy
  • Aliases:
    • airway allergy
Homo sapiens (human)
DOID:0060318
  • acute promyelocytic leukemia
  • Aliases:
    • acute myeloblastic leukaemia type 3
    • acute myeloblastic leukemia type 3
    • acute myeloid leukaemia M3
    • acute myeloid leukemia M3
    • acute promyelocytic leukaemia
Homo sapiens (human)
DOID:0111144
  • preterm premature rupture of the membranes
  • Aliases:
    • PPROM
Homo sapiens (human)
DOID:3410
  • carotid artery thrombosis
Homo sapiens (human)
DOID:12531
  • von Willebrand's disease
  • Aliases:
    • vascular hemophilia
    • vascular pseudohemophilia
    • von Willebrand disease
    • von Willebrand disorder
    • von Willebrand's-Jurgens' disease
    • von Willebrand-Jrgens disease
Homo sapiens (human)
DOID:4138
  • bile duct disease
  • Aliases:
    • bile duct disorder
    • disorder of bile duct
Homo sapiens (human)
DOID:11512
  • Budd-Chiari syndrome
  • Aliases:
    • hepatic vein thrombosis
Homo sapiens (human)
DOID:8483
  • retinal artery occlusion
Homo sapiens (human)
DOID:2216
  • factor V deficiency
  • Aliases:
    • Hereditary hypoproaccelerinaemia
    • Labile factor deficiency
    • Proaccelerin deficiency
    • deficiency, labile
Homo sapiens (human)
DOID:999
  • hypereosinophilic syndrome
  • Aliases:
    • Eosinophilic leukocytosis
    • eosinophilia
Homo sapiens (human)
DOID:0111902
  • thrombophilia due to activated protein C resistance
  • Aliases:
    • APC resistance
    • PCCF deficiency
    • PROC cofactor deficiency
    • THPH2
    • activated protein C resistance
    • thrombophilia V
    • thrombophilia due to deficiency of activated protein C cofactor
Homo sapiens (human)
DOID:0111231
  • congenital muscular dystrophy-dystroglycanopathy type A8
  • Aliases:
    • MDDGA8
    • Walker-Warburg syndrome or muscle-eye-brain disease GTDC2-related
    • congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A8
Mus musculus (house mouse)
DOID:0112382
  • muscular dystrophy-dystroglycanopathy type C8
  • Aliases:
    • LGMDR24
    • MDDGC2
    • autosomal recessive limb-girdle muscular dystrophy 24
    • muscular dystrophy-dystroglycanopathy (limb-girdle) type C, 8
    • muscular dystrophy-dystroglycanopathy, limb-girdle, POMGNT2-related
Mus musculus (house mouse)
DOID:2215
  • factor VII deficiency
  • Aliases:
    • deficiency, stable
Homo sapiens (human)
DOID:0070338
  • cerebellar hypoplasia
Mus musculus (house mouse)
DOID:0060574
  • von Willebrand's disease 2
  • Aliases:
    • VWD type 2
    • VWD2
    • von Willebrand disease type 2
    • von Willebrand disease type II
Homo sapiens (human)
DOID:801
  • hemarthrosis
  • Aliases:
    • Haemarthrosis of shoulder joint
    • Haemarthrosis of the ankle and foot
    • Haemarthrosis of the pelvic region and thigh
    • Hemarthrosis involving ankle and foot
    • Hemarthrosis involving forearm
    • Hemarthrosis involving hand
    • Hemarthrosis involving lower leg
    • Hemarthrosis involving pelvic region and thigh
    • Hemarthrosis involving shoulder region
    • Hemarthrosis involving upper arm
    • Hemarthrosis of ankle and/or foot
    • Hemarthrosis of forearm
    • Hemarthrosis of hand
    • Hemarthrosis of lower leg
    • Hemarthrosis of shoulder
    • Hemarthrosis of shoulder region
    • Hemarthrosis of the ankle and foot
    • Hemarthrosis of the ankle and/or foot
    • Hemarthrosis of the forearm
    • Hemarthrosis of the hand
    • Hemarthrosis of the lower leg
    • Hemarthrosis of the pelvic region and thigh
    • Hemarthrosis of the shoulder region
    • Hemarthrosis of the upper arm
    • Hemarthrosis of upper arm
Homo sapiens (human)
DOID:0080839
  • X-linked warfarin sensitivity
Homo sapiens (human)
DOID:0111899
  • X-linked thrombophilia due to factor IX defect
  • Aliases:
    • THPH8
Homo sapiens (human)

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Last updated: December 9, 2024