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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 14926 - 14950 of 15957 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism Source
DOID:0060178
  • familial hemiplegic migraine
Homo sapiens (human)
DOID:0112348
  • hereditary spastic paraplegia 78
  • Aliases:
    • SPG78
    • spastic paraplegia 78 autosomal recessive
Homo sapiens (human)
DOID:0060893
  • juvenile-onset Parkinson's disease
  • Aliases:
    • juvenile-onset Parkinson disease
Homo sapiens (human)
DOID:0060556
  • Kufor-Rakeb syndrome
  • Aliases:
    • autosomal recessive Parkinson disease 9
    • autosomal recessive juvenile onset Parkinson disease 9
Homo sapiens (human)
DOID:14503
  • neuronal ceroid lipofuscinosis
  • Aliases:
    • hereditary ceroid lipofuscinosis
Homo sapiens (human)
DOID:0070221
  • progressive familial intrahepatic cholestasis
  • Aliases:
    • PFIC; Byler disease
Homo sapiens (human)
DOID:0060162
  • dentatorubral-pallidoluysian atrophy
  • Aliases:
    • DRPLA
    • Haw River Syndrome
    • Naito-Oyanagi disease
Homo sapiens (human)
DOID:9655
  • oral mucosa leukoplakia
Homo sapiens (human)
DOID:14566
  • disease of cellular proliferation
  • Aliases:
    • cell process disease
    • neoplasm
Homo sapiens (human)
DOID:0050671
  • female breast cancer
Homo sapiens (human)
DOID:0060058
  • lymphoma
  • Aliases:
    • lymphoid cancer
Homo sapiens (human)
DOID:9669
  • senile cataract
Homo sapiens (human)
DOID:3969
  • thyroid gland papillary carcinoma
  • Aliases:
    • Papillary carcinoma of the Thyroid gland
Homo sapiens (human)
DOID:5223
  • infertility
Homo sapiens (human)
DOID:12704
  • ataxia telangiectasia
  • Aliases:
    • Boder-Sedgwick syndrome
    • Louis Bar syndrome
Homo sapiens (human)
DOID:0070154
  • hereditary sensory neuropathy type 1F
  • Aliases:
    • HSN1F
    • hereditary sensory neuropathy type IF
Homo sapiens (human)
DOID:0110791
  • hereditary spastic paraplegia 3A
  • Aliases:
    • FSP1
    • SPG3A
    • autosomal dominant familial spastic paraplegia 1
    • autosomal dominant spastic paraplegia 3
    • autosomal dominant spastic paraplegia type 3
    • strumpell disease
Homo sapiens (human)
DOID:653
  • purine-pyrimidine metabolic disorder
  • Aliases:
    • inborn errors of purine-pyrimidine metabolism
Homo sapiens (human)
DOID:0080540
  • galactosialidosis
Saccharomyces cerevisiae S288C
DOID:3211
  • lysosomal storage disease
  • Aliases:
    • disorder of lysosomal enzyme
    • inborn lysosomal enzyme disorder
    • lysosomal storage metabolism disorder
Saccharomyces cerevisiae S288C
DOID:11151
  • cholecystolithiasis
Saccharomyces cerevisiae S288C
DOID:2739
  • Gilbert syndrome
  • Aliases:
    • Constitutional hyperbilirubinemia
    • Gilbert's disease
    • Gilbert's syndrome
    • Gilbert-Meulengracht syndrome
    • hereditary nonhemolytic jaundice
Saccharomyces cerevisiae S288C
DOID:2043
  • hepatitis B
  • Aliases:
    • chronic hepatitis B
    • hepatitis B infection
Saccharomyces cerevisiae S288C
DOID:3803
  • Crigler-Najjar syndrome
  • Aliases:
    • Bilirubin UDP glucuronyl transferase deficiency
    • Crigler Najjar syndrome
    • Crigler-Najjar syndrome, type I
Saccharomyces cerevisiae S288C
DOID:8692
  • myeloid leukemia
  • Aliases:
    • Non-Lymphocytic Leukemia
    • leukaemia myelogenous
    • leukemia myelogenous
    • myeloid granulocytic leukaemia
    • myeloid granulocytic leukemia
    • myeloid leukaemia
Saccharomyces cerevisiae S288C
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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