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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 3576 - 3600 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Organism Source
DOID:11720
  • distal myopathy
  • Aliases:
    • distal muscular dystrophy
Mus musculus (house mouse)
DOID:0080719
  • congenital myopathy 6
  • Aliases:
    • inclusion body myopathy 3
    • proximal myopathy and ophthalmoplegia
Mus musculus (house mouse)
DOID:0111269
  • autosomal dominant hyaline body myopathy
  • Aliases:
    • MSMA
    • Myopathy, myosin storage, autosomal dominant
    • congenital myopathy 7A
    • myopathy with lysis of type I myofibrils
Mus musculus (house mouse)
DOID:0111605
  • distal arthrogryposis type 2A
  • Aliases:
    • DA2A
    • distal arthrogryposis type 2A (Freeman-Sheldon)
Mus musculus (house mouse)
DOID:0111596
  • distal arthrogryposis type 1
  • Aliases:
    • DA1
    • digitotalar dysmorphism
Mus musculus (house mouse)
DOID:2106
  • myotonia congenita
  • Aliases:
    • Batten Turner congenital myopathy
    • Thomsen and Becker disease
Mus musculus (house mouse)
DOID:0110454
  • dilated cardiomyopathy 1S
  • Aliases:
    • CMD1S
Mus musculus (house mouse)
DOID:0111602
  • distal arthrogryposis type 2B3
  • Aliases:
    • DA2B3
    • distal arthrogryposis type 2B3 (Sheldon-Hall)
Mus musculus (house mouse)
DOID:0111268
  • autosomal recessive hyaline body myopathy
  • Aliases:
    • MSMB
    • Myopathy, myosin storage, autosomal recessive
    • congenital myopathy 7B
Mus musculus (house mouse)
DOID:0070197
  • distal myopathy 1
  • Aliases:
    • Distal myopathy type 1
    • Gowers disease
    • Laing distal myopathy
    • Laing early-onset distal myopathy
    • MPD1
Mus musculus (house mouse)
DOID:0110307
  • hypertrophic cardiomyopathy 1
  • Aliases:
    • CMH1
    • cardiomyopathy, familial hypertrophic 1
    • hypertrophic cardiomyopathy 19
Mus musculus (house mouse)
DOID:0060394
  • chromosome 15q13.3 microdeletion syndrome
  • Aliases:
    • 15q13.3 microdeletion syndrome
Homo sapiens (human)
DOID:896
  • metal metabolism disorder
  • Aliases:
    • inborn metal metabolism disorder
Homo sapiens (human)
DOID:0060883
  • intestinal hypomagnesemia 1
  • Aliases:
    • HOMG1
    • hypomagnesemia caused by selective magnesium malabsorption
    • hypomagnesemia intestinal type 1
    • hypomagnesemic tetany
    • intestinal hypomagnesemia with secondary hypocalcemia
    • primary hypomagnesemia with secondary hypocalcemia
Homo sapiens (human)
DOID:9975
  • cocaine dependence
Rattus norvegicus (Norway rat)
DOID:2030
  • anxiety disorder
  • Aliases:
    • anxiety
    • anxiety state
Rattus norvegicus (Norway rat)
DOID:594
  • panic disorder
  • Aliases:
    • panic anxiety syndrome
Rattus norvegicus (Norway rat)
DOID:13636
  • Fanconi anemia
  • Aliases:
    • Fanconi anaemia
    • Fanconi pancytopenia
    • Fanconi panmyelopathy
    • Fanconi's anaemia
    • Fanconi's anemia
Mus musculus (house mouse)
DOID:0111095
  • Fanconi anemia complementation group A
  • Aliases:
    • FANCA
Mus musculus (house mouse)
DOID:0080093
  • myofibrillar myopathy 2
  • Aliases:
    • alpha-b crystallinopathy
Homo sapiens (human)
DOID:9870
  • galactosemia
  • Aliases:
    • Galactosaemia
    • Galactose intolerance
Homo sapiens (human)
DOID:0110174
  • Charcot-Marie-Tooth disease axonal type 2L
  • Aliases:
    • CMT2L
    • Charcot-Marie-Tooth neuropathy axonal type 2L
    • autosomal dominant Charcot-Marie-Tooth disease type 2L
    • autosomal dominant axonal Charcot-Marie-Tooth disease type 2L
Homo sapiens (human)
DOID:0111206
  • autosomal dominant distal hereditary motor neuronopathy 2
  • Aliases:
    • HMN II
    • HMN IIA
    • HMN2
    • HMN2A
    • autosomal dominant adult spinal muscular atrophy IIA
    • distal hereditary motor neuronopathy type 2
    • distal hereditary motor neuronopathy type 2A
    • distal hereditary motor neuropathy type II
    • distal hereditary motor neuropathy type IIA
    • spinal Charcot-Marie-Tooth disease IIA
Homo sapiens (human)
DOID:9282
  • ocular hypertension
Homo sapiens (human)
DOID:0110266
  • cataract 9 multiple types
  • Aliases:
    • CTRCT9
    • cataract 9 multiple types with or without microcornea
Homo sapiens (human)
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Last updated: December 9, 2024