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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 10426 - 10450 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼ Source
DOID:1498
  • cholera
  • Aliases:
    • Cholera - Vibrio cholerae
    • Cholera due to Vibrio cholerae
    • Vibrio cholerae
Homo sapiens (human)
DOID:8704
  • genital herpes
  • Aliases:
    • Genital herpes simplex
    • Herpes Genitalis
    • Virus-Genital Herpes
    • venereal herpes
Homo sapiens (human)
DOID:0110372
  • retinitis pigmentosa 4
  • Aliases:
    • RP4
Homo sapiens (human)
DOID:4248
  • coronary stenosis
  • Aliases:
    • Coronary artery stenosis
Homo sapiens (human)
DOID:11266
  • Hantavirus hemorrhagic fever with renal syndrome
  • Aliases:
    • HFRS
    • Hemorrhagic fever, Russian
    • Hemorrhagic nephrosonephritis
    • Puumala virus nephropathy
Homo sapiens (human)
DOID:0080468
  • developmental and epileptic encephalopathy 1
  • Aliases:
    • DEE1
    • X-linked infantile spasm syndrome 1
    • early infantile epileptic encephalopathy 1
Homo sapiens (human)
DOID:8645
  • subacute delirium
Homo sapiens (human)
DOID:3322
  • GM1 gangliosidosis
  • Aliases:
    • Beta-galactosidase deficiency
    • deficiency of beta-galactosidase
    • gangliosidosis GM1
Homo sapiens (human)
DOID:12800
  • mucopolysaccharidosis VI
  • Aliases:
    • MPS VI - Maroteaux-Lamy syndrome
    • Maroteaux - Lamy syndrome
    • Maroteaux-Lamy syndrome
    • arylsulfatase B deficiency
    • deficiency of N-acetylgalactosamine-4-sulfatase
Homo sapiens (human)
DOID:0090144
  • Donnai-Barrow syndrome
  • Aliases:
    • DBS/FOAR syndrome
    • FOAR syndrome
    • Holmes-Schepens syndrome
    • diaphragmatic hernia, exomphalos, absent corpus callosum, hypertelorism, myopia, sensorineural deafness, and proteinuria
    • diaphragmatic hernia-exomphalos-hypertelorism syndrome
    • diaphragmatic hernia-hypertelorism-myopia-deafness syndrome
    • facio-oculo-acoustico-renal syndrome
    • faciooculoacousticorenal syndrome
    • syndrome of ocular and facial anomalies, telecanthus and deafness
Homo sapiens (human)
DOID:853
  • polymyalgia rheumatica
Homo sapiens (human)
DOID:0080409
  • familial adenomatous polyposis 1
Homo sapiens (human)
DOID:0110540
  • autosomal recessive nonsyndromic deafness 98
  • Aliases:
    • DFNB98
    • autosomal recessive deafness 98
Homo sapiens (human)
DOID:0060872
  • isolated growth hormone deficiency type II
  • Aliases:
    • IGHD II
    • autosomal dominant isolated growth hormone deficiency
    • autosomal dominant pituitary dwarfism due to isolated growth hormone deficiency
    • congenital IGHD type II
    • congenital isolated GH deficiency type II
    • congenital isolated growth hormone deficiency type II
Homo sapiens (human)
DOID:0080328
  • Culler-Jones syndrome
Homo sapiens (human)
DOID:0070539
  • Halperin-Birk syndrome
  • Aliases:
    • HLBKS
    • NEDSOSB
    • NEURODEVELOPMENTAL DISORDER WITH SPASTIC QUADRIPLEGIA, OPTIC ATROPHY, SEIZURES, AND STRUCTURAL BRAIN ANOMALIES
Homo sapiens (human)
DOID:0070345
  • vertebral anomalies and variable endocrine and T-cell dysfunction
  • Aliases:
    • heterozygotes for TBX2 variants
Homo sapiens (human)
DOID:4166
  • syphilis
  • Aliases:
    • syphilitic chancre
Homo sapiens (human)
DOID:9282
  • ocular hypertension
Homo sapiens (human)
DOID:3326
  • purpura
  • Aliases:
    • Purpuric disorder
Homo sapiens (human)
DOID:2326
  • gastroenteritis
  • Aliases:
    • cholera morbus
    • infectious colitis, enteritis and gastroenteritis
Homo sapiens (human)
DOID:13963
  • nuclear senile cataract
  • Aliases:
    • Senile nuclear cataract
    • Senile nuclear sclerosis
Homo sapiens (human)
DOID:0070154
  • hereditary sensory neuropathy type 1F
  • Aliases:
    • HSN1F
    • hereditary sensory neuropathy type IF
Homo sapiens (human)
DOID:0111769
  • 46,XY sex reversal 6
  • Aliases:
    • 46,XY gonadal dysgenesis, partial or complete, MAP3K1-related
    • 46,XY sex reversal, partial or complete, MAP3K1-related
    • SRXY6
Homo sapiens (human)
DOID:13636
  • Fanconi anemia
  • Aliases:
    • Fanconi anaemia
    • Fanconi pancytopenia
    • Fanconi panmyelopathy
    • Fanconi's anaemia
    • Fanconi's anemia
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