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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 3451 - 3475 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Organism Source
DOID:0070041
  • autosomal dominant intellectual developmental disorder 11
  • Aliases:
    • MRD11
    • autosomal dominant mental retardation 11
    • autosomal dominant non-syndromic intellectual disability 11
Mus musculus (house mouse)
DOID:0110229
  • cataract 6 multiple types
  • Aliases:
    • CTRCT6
Mus musculus (house mouse)
DOID:0110734
  • neurodegeneration with brain iron accumulation
  • Aliases:
    • NBIA
Homo sapiens (human)
DOID:264
  • hemangiopericytoma
  • Aliases:
    • Haemangiopericytic meningioma
    • hemangiopericytoma, malignant
    • malignant hemangiopericytoma
Mus musculus (house mouse)
DOID:75
  • lymphatic system disease
  • Aliases:
    • Lymphangiopathy
    • Lymphatic disease
    • disease of lympoid system
    • disorder of lymph node and lymphatics
    • disorder of lymphatic system
    • disorder of lymphoid system
    • lymphatic disorder
    • lympoid system disease
Mus musculus (house mouse)
DOID:0081030
  • central conducting lymphatic anomaly
  • Aliases:
    • lymphatic malformation-7
Mus musculus (house mouse)
DOID:1579
  • respiratory system disease
Mus musculus (house mouse)
DOID:0080001
  • bone disease
Mus musculus (house mouse)
DOID:5022
  • aflatoxins-related hepatocellular carcinoma
Mus musculus (house mouse)
DOID:705
  • Leber hereditary optic neuropathy
  • Aliases:
    • Leber's hereditary optic neuropathy
    • Leber's optic atrophy
Mus musculus (house mouse)
DOID:10320
  • asbestosis
Mus musculus (house mouse)
DOID:11870
  • Pick's disease
  • Aliases:
    • Dementia in Pick's disease
    • LOBAR ATROPHY OF BRAIN
    • PICK DISEASE OF BRAIN
    • Pick disease
Homo sapiens (human)
DOID:11206
  • opioid abuse
Homo sapiens (human)
DOID:9973
  • substance dependence
Homo sapiens (human)
DOID:13268
  • porphyria
  • Aliases:
    • Hematoporphyria
    • Porphyrinopathy
    • disorder of porphyrin and hem metabolism
    • disorder of porphyrin metabolism
Mus musculus (house mouse)
DOID:0080290
  • familial erythrocytosis 5
  • Aliases:
    • ECYT5
Mus musculus (house mouse)
DOID:13413
  • hepatic encephalopathy
  • Aliases:
    • Portal-systemic encephalopathy
Mus musculus (house mouse)
DOID:0060652
  • familial erythrocytosis 1
  • Aliases:
    • ECYT1
    • autosomal dominant benign erythrocytosis
    • primary familial and congenital polycythemia
Mus musculus (house mouse)
DOID:11049
  • meconium aspiration syndrome
  • Aliases:
    • Neonatal aspiration of meconium
    • meconium aspiration
Homo sapiens (human)
DOID:0110463
  • autosomal recessive nonsyndromic deafness 102
  • Aliases:
    • DFNB102
    • autosomal recessive deafness 102
Mus musculus (house mouse)
DOID:10376
  • amblyopia
  • Aliases:
    • lazy eye
Mus musculus (house mouse)
DOID:13133
  • HELLP syndrome
Mus musculus (house mouse)
DOID:3443
  • mammary Paget's disease
  • Aliases:
    • Paget cell neoplasm
    • Paget's disease
    • Paget's disease of the breast
    • mammary Paget disease
Mus musculus (house mouse)
DOID:0080679
  • neuronal intestinal dysplasia type A
Mus musculus (house mouse)
DOID:0060560
  • lethal congenital contracture syndrome 2
  • Aliases:
    • LCCS2
    • multiple contracture syndrome, Israeli-Bedouin type
Mus musculus (house mouse)
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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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

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Last updated: December 9, 2024