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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 13376 - 13400 of 15957 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism Source
DOID:2513
  • basal cell carcinoma
  • Aliases:
    • Basal cell cancer
    • Basal cell carcinoma of skin
    • Basal cell neoplasm
    • Basal cell tumor
    • Epithelioma basal cell
    • Rodent ulcer
    • malignant Basal cell neoplasm
    • malignant basal cell tumor
Homo sapiens (human)
DOID:7474
  • malignant pleural mesothelioma
  • Aliases:
    • malignant mesothelioma of pleura
Homo sapiens (human)
DOID:6039
  • uveal melanoma
  • Aliases:
    • melanoma of Uvea
Homo sapiens (human)
DOID:14654
  • prostatitis
Homo sapiens (human)
DOID:11119
  • Gilles de la Tourette syndrome
  • Aliases:
    • Guinon's disease
    • Psychogenic tics
    • Tourette syndrome
    • motor-verbal tic disorder
Homo sapiens (human)
DOID:9253
  • gastrointestinal stromal tumor
  • Aliases:
    • GANT
    • GIST
    • Stromal tumor of gastrointestinal tract
    • Stromal tumour of gastrointestinal tract
    • gastrointestinal stromal tumour
Homo sapiens (human)
DOID:0110448
  • dilated cardiomyopathy 1HH
  • Aliases:
    • CMD1HH
Homo sapiens (human)
DOID:0080097
  • myofibrillar myopathy 6
Homo sapiens (human)
DOID:3669
  • intermittent claudication
  • Aliases:
    • Charcot's syndrome
Homo sapiens (human)
DOID:0111954
  • immunodeficiency 60
  • Aliases:
    • BACH2-related immunodeficiency and autoimmunity
    • BRIDA
    • IMD60
Homo sapiens (human)
DOID:9255
  • frontotemporal dementia
  • Aliases:
    • Wilhemsen-Lynch disease
    • frontotemporal lobar degeneration
    • multiple system tauopathy with presenile dementia
    • pallidopontonigral degeneration
Homo sapiens (human)
DOID:2491
  • sensory peripheral neuropathy
  • Aliases:
    • peripheral Sensory Neuropathy
    • sensory neuropathy
Homo sapiens (human)
DOID:0111238
  • congenital muscular dystrophy-dystroglycanopathy type A13
  • Aliases:
    • MDDGA13
    • Walker-Warburg syndrome or muscle-eye-brain disease, B3GNT1-related
    • Walker-Warburg syndrome or muscle-eye-brain disease, B4GNT1-related
    • congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A13
Rattus norvegicus (Norway rat)
DOID:0050560
  • Walker-Warburg syndrome
  • Aliases:
    • HARD syndrome
    • cerebroocular dysplasia-muscular dystrophy syndrome
Rattus norvegicus (Norway rat)
DOID:0050588
  • muscular dystrophy-dystroglycanopathy type B1
  • Aliases:
    • CMD due to dystroglycanopathy
    • Muscular dystrophy-dystroglycanopathy congenital with impaired intellectual development B1
Rattus norvegicus (Norway rat)
DOID:0111238
  • congenital muscular dystrophy-dystroglycanopathy type A13
  • Aliases:
    • MDDGA13
    • Walker-Warburg syndrome or muscle-eye-brain disease, B3GNT1-related
    • Walker-Warburg syndrome or muscle-eye-brain disease, B4GNT1-related
    • congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A13
Mus musculus (house mouse)
DOID:0050588
  • muscular dystrophy-dystroglycanopathy type B1
  • Aliases:
    • CMD due to dystroglycanopathy
    • Muscular dystrophy-dystroglycanopathy congenital with impaired intellectual development B1
Mus musculus (house mouse)
DOID:0050560
  • Walker-Warburg syndrome
  • Aliases:
    • HARD syndrome
    • cerebroocular dysplasia-muscular dystrophy syndrome
Mus musculus (house mouse)
DOID:0080738
  • Ehlers-Danlos syndrome spondylodysplastic type 1
Rattus norvegicus (Norway rat)
DOID:0080738
  • Ehlers-Danlos syndrome spondylodysplastic type 1
Mus musculus (house mouse)
DOID:0070256
  • congenital disorder of glycosylation type IId
  • Aliases:
    • CDG IId
    • CDG2D
    • CDGIId
Rattus norvegicus (Norway rat)
DOID:0070256
  • congenital disorder of glycosylation type IId
  • Aliases:
    • CDG IId
    • CDG2D
    • CDGIId
Mus musculus (house mouse)
DOID:28
  • endocrine system disease
Mus musculus (house mouse)
DOID:0110777
  • hereditary spastic paraplegia 26
  • Aliases:
    • GM2 synthase deficiency
    • SPG26
    • autosomal recessive spastic paraplegia 26
    • autosomal recessive spastic paraplegia type 26
Rattus norvegicus (Norway rat)
DOID:0110777
  • hereditary spastic paraplegia 26
  • Aliases:
    • GM2 synthase deficiency
    • SPG26
    • autosomal recessive spastic paraplegia 26
    • autosomal recessive spastic paraplegia type 26
Mus musculus (house mouse)
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Last updated: December 9, 2024