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 6176 - 6200 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Organism Source
DOID:0060767
  • autosomal dominant Robinow syndrome 3
  • Aliases:
    • DRS3
Homo sapiens (human)
DOID:9279
  • hyperhomocysteinemia
Homo sapiens (human)
DOID:0070037
  • autosomal dominant intellectual developmental disorder 7
  • Aliases:
    • DYRK1A syndrome
    • MRD7
    • autosomal dominant mental retardation 7
    • autosomal dominant non-syndromic intellectual disability 7
Homo sapiens (human)
DOID:0060230
  • basal ganglia calcification
  • Aliases:
    • Fahr disease
Mus musculus (house mouse)
DOID:4586
  • familial meningioma
Mus musculus (house mouse)
DOID:4202
  • brain stem glioma
  • Aliases:
    • Brainstem Neuroglial tumor
Mus musculus (house mouse)
DOID:3840
  • craniopharyngioma
  • Aliases:
    • neoplasm of Rathke's Pouch
Mus musculus (house mouse)
DOID:4297
  • scimitar syndrome
  • Aliases:
    • Halasz syndrome
    • congenital venolobar syndrome
    • hypogenetic lung syndrome
    • mirror-image lung syndrome
    • pulmonary venolobar syndrome
    • total anomalous pulmonary venous return
    • vena cava bronchovascular syndrome
Mus musculus (house mouse)
DOID:0111344
  • myeloproliferative disorder with eosinophilia
  • Aliases:
    • chronic myeloproliferative disorder with eosinophilia
Mus musculus (house mouse)
DOID:8946
  • severe nonproliferative diabetic retinopathy
  • Aliases:
    • High risk non proliferative diabetic retinopathy
    • Severe NPDR
Mus musculus (house mouse)
DOID:3649
  • pyruvate decarboxylase deficiency
  • Aliases:
    • deficiency of pyruvic dehydrogenase
    • pyruvate dehydrogenase complex deficiency disease
    • pyruvate dehydrogenase deficiency
Mus musculus (house mouse)
DOID:1214
  • tympanosclerosis
Mus musculus (house mouse)
DOID:0050644
  • arterial calcification of infancy
  • Aliases:
    • generalized arterial calcification of infancy
    • idiopathic infantile arterial calcification
    • infantile arteriosclerosis
Mus musculus (house mouse)
DOID:0111103
  • maturity-onset diabetes of the young type 4
  • Aliases:
    • MODY type 4
    • MODY4
Mus musculus (house mouse)
DOID:0050877
  • pancreatic agenesis
  • Aliases:
    • Agenesis of the dorsal pancreas
    • partial pancreatic agenesis
Mus musculus (house mouse)
DOID:543
  • dystonia
  • Aliases:
    • dystonic disease
Homo sapiens (human)
DOID:0060730
  • torsion dystonia 1
  • Aliases:
    • dystonia musculorum deformans
Homo sapiens (human)
DOID:0080981
  • arthrogryposis multiplex congenita-5
Homo sapiens (human)
DOID:0050836
  • focal dystonia
Homo sapiens (human)
DOID:9643
  • babesiosis
  • Aliases:
    • Babesiasis
    • Infection by babesia
    • piroplasmosis
Mus musculus (house mouse)
DOID:0050853
  • chronic venous insufficiency
Mus musculus (house mouse)
DOID:0060564
  • spinal disease
Mus musculus (house mouse)
DOID:0050628
  • advanced sleep phase syndrome
  • Aliases:
    • familial advanced sleep-phase syndrome
Mus musculus (house mouse)
DOID:0110011
  • advanced sleep phase syndrome 1
  • Aliases:
    • FASPS1
    • familial advanced sleep phase syndrome 1
Mus musculus (house mouse)
DOID:0111768
  • X-linked properdin deficiency
  • Aliases:
    • CFPD
    • complement factor properdin deficiency
Mus musculus (house mouse)

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Last updated: December 9, 2024