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 7251 - 7275 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼ Source
DOID:0110291
  • Leber congenital amaurosis 10
  • Aliases:
    • LCA10
Mus musculus (house mouse)
DOID:3191
  • nemaline myopathy
  • Aliases:
    • Nemaline body disease
    • nemaline rod myopathy
    • rod body disease
    • rod myopathy
Mus musculus (house mouse)
DOID:0080348
  • Alzheimer's disease 1
  • Aliases:
    • Alzheimer's disease 1, early onset
Mus musculus (house mouse)
DOID:0111215
  • autosomal dominant distal hereditary motor neuronopathy 8
  • Aliases:
    • DHMN8
    • HMN8
    • autosomal dominant benign distal spinal muscular atrophy
    • autosomal dominant congenital benign spinal muscular atrophy
    • congenital benign spinal muscular atrophy with contractures
    • congenital nonprogressive spinal muscular atrophy
    • distal hereditary motor neuronopathy type 8
    • distal hereditary motor neuropathy type VIII
Mus musculus (house mouse)
DOID:9883
  • Becker muscular dystrophy
  • Aliases:
    • Benign pseudohypertrophic muscular dystrophy
    • benign congenital myopathy
Mus musculus (house mouse)
DOID:0080006
  • bone development disease
Mus musculus (house mouse)
DOID:0080036
  • SOST-related sclerosing bone dysplasia
  • Aliases:
    • van Buchem disease
Mus musculus (house mouse)
DOID:0080576
  • spondyloepimetaphyseal dysplasia, Genevieve-type
Mus musculus (house mouse)
DOID:0112281
  • spondyloepiphyseal dysplasia Stanescu type
  • Aliases:
    • SED Stanescu type
    • SEDSTN
Mus musculus (house mouse)
DOID:0080941
  • acquired angioedema
Mus musculus (house mouse)
DOID:5463
  • cochlear disease
Mus musculus (house mouse)
DOID:8553
  • pyoderma gangrenosum
Mus musculus (house mouse)
DOID:0080821
  • exercise-induced bronchoconstriction
  • Aliases:
    • exercise-induced asthma
Mus musculus (house mouse)
DOID:0050456
  • Buruli ulcer disease
  • Aliases:
    • Bairnsdale ulcer
    • Daintree ulcer
    • Mossman ulcer
    • Searl ulcer
    • Searle's ulcer
Mus musculus (house mouse)
DOID:0081017
  • congenital fibrosis of the extraocular muscles 3A
Mus musculus (house mouse)
DOID:11726
  • Emery-Dreifuss muscular dystrophy
  • Aliases:
    • EDMD
Mus musculus (house mouse)
DOID:0111903
  • thrombophilia due to HRG deficiency
  • Aliases:
    • THPH11
    • hereditary thrombophilia due to congenital HRG deficiency
    • hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency
Mus musculus (house mouse)
DOID:7474
  • malignant pleural mesothelioma
  • Aliases:
    • malignant mesothelioma of pleura
Mus musculus (house mouse)
DOID:0111330
  • combined saposin deficiency
  • Aliases:
    • PSAPD
    • combined SAP deficiency
    • encephalopathy due to prosaposin deficiency
Mus musculus (house mouse)
DOID:0060746
  • basal laminar drusen
  • Aliases:
    • cuticular drusen
    • drusen of bruch membrane
    • early adult-onset grouped drusen
Mus musculus (house mouse)
DOID:8483
  • retinal artery occlusion
Mus musculus (house mouse)
DOID:0111277
  • mitochondrial trifunctional protein deficiency
  • Aliases:
    • MTPD
    • TFP deficiency
    • TFPD
Mus musculus (house mouse)
DOID:0112121
  • nephrogenic syndrome of inappropriate antidiuresis
  • Aliases:
    • NSIAD
Mus musculus (house mouse)
DOID:0050475
  • Weill-Marchesani syndrome
  • Aliases:
    • GEMSS syndrome
    • Marchesani-Weill Syndrome
    • Mesodermal Dysmorphodystrophy, Congenital
    • Spherophakia Brachymorphia Syndrome
    • congenital mesodermal dystrophy
Mus musculus (house mouse)
DOID:4906
  • small intestine adenocarcinoma
  • Aliases:
    • small intestinal adenocarcinoma
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