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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 9051 - 9075 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Organism Source
DOID:0060793
  • hypomyelinating leukodystrophy 5
  • Aliases:
    • HLD5
    • hypomyelination-congenital cataract syndrome
Homo sapiens (human)
DOID:14320
  • generalized anxiety disorder
Homo sapiens (human)
DOID:0060227
  • Adams-Oliver syndrome
  • Aliases:
    • Adams Oliver syndrome
Homo sapiens (human)
DOID:0050441
  • mucosulfatidosis
  • Aliases:
    • Sulfatidosis, Juvenile, Austin Type
    • multiple sulfatase deficiency disease
Homo sapiens (human)
DOID:0110668
  • congenital myasthenic syndrome 10
  • Aliases:
    • CMS10
    • LGM
    • congenital muscular dystrophy merosin-positive
    • familial limb-girdle myasthenia
Homo sapiens (human)
DOID:0111376
  • fetal akinesia deformation sequence syndrome 3
  • Aliases:
    • FADS3
Homo sapiens (human)
DOID:0111789
  • Frank-Ter Haar syndrome
  • Aliases:
    • Borrone dermatocardioskeletal syndrome
    • FTHS
    • Ter Haar syndrome
    • autosomal recessive Melnick-Needles syndrome
    • megalocornea, multiple skeletal anomalies, and developmental delay
Homo sapiens (human)
DOID:0112353
  • spermatogenic failure 64
  • Aliases:
    • SPGF64
Homo sapiens (human)
DOID:0111134
  • focal segmental glomerulosclerosis 9
  • Aliases:
    • FSGS9
Homo sapiens (human)
DOID:0111625
  • ventriculomegaly - cystic kidney disease
  • Aliases:
    • VMCKD
    • congenital nephrosis-cerebral ventriculomegaly syndrome
    • cystic kidney disease with ventriculomegaly
    • ventriculomegaly with cystic kidney disease
Homo sapiens (human)
DOID:0110526
  • autosomal recessive nonsyndromic deafness 79
  • Aliases:
    • DFNB79
    • autosomal recessive deafness 79
Homo sapiens (human)
DOID:0112274
  • X-linked spermatogenic failure 3
  • Aliases:
    • SPGFX3
Homo sapiens (human)
DOID:0110500
  • autosomal recessive nonsyndromic deafness 42
  • Aliases:
    • DFNB42
    • autosomal recessive deafness 42
Homo sapiens (human)
DOID:9452
  • steatotic liver disease
  • Aliases:
    • Fatty change of liver
    • SLD
    • Steatosis of liver
    • alcoholic fatty liver
    • fatty liver disease
    • hepatic lipidosis
    • hepatic steatosis
Danio rerio (zebrafish)
DOID:11446
  • sciatic neuropathy
Danio rerio (zebrafish)
DOID:11981
  • morbid obesity
  • Aliases:
    • Severe obesity
Danio rerio (zebrafish)
DOID:0080547
  • metabolic dysfunction-associated steatohepatitis
  • Aliases:
    • MASH
    • NASH
    • non-alcoholic steatohepatitis
    • nonalcoholic steatohepatitis
Danio rerio (zebrafish)
DOID:2030
  • anxiety disorder
  • Aliases:
    • anxiety
    • anxiety state
Danio rerio (zebrafish)
DOID:0080095
  • myofibrillar myopathy 4
  • Aliases:
    • zaspopathy
Rattus norvegicus (Norway rat)
DOID:0080096
  • myofibrillar myopathy 5
  • Aliases:
    • filaminopathy
Mus musculus (house mouse)
DOID:0111190
  • distal myopathy 4
  • Aliases:
    • MPD4
    • distal ABD-filaminopathy
    • distal muscular dystrophy 4
    • distal myopathy with posterior leg and anterior hand involvement
Mus musculus (house mouse)
DOID:0050680
  • Boomerang dysplasia
Mus musculus (house mouse)
DOID:14764
  • Larsen syndrome
  • Aliases:
    • dominant larsen syndrome
Mus musculus (house mouse)
DOID:13839
  • extrapyramidal and movement disease
Rattus norvegicus (Norway rat)
DOID:0111700
  • ankyrin-B-related cardiac arrhythmia
  • Aliases:
    • ankyrin-B syndrome
Homo sapiens (human)
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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