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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 10326 - 10350 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Organism Source
DOID:4990
  • essential tremor
  • Aliases:
    • benign essential tremor
    • essential hereditary tremor
    • shaky hand syndrome
Drosophila melanogaster (fruit fly)
DOID:251
  • alcohol-induced mental disorder
Drosophila melanogaster (fruit fly)
DOID:0111428
  • essential tremor 1
  • Aliases:
    • ETM1
    • hereditary essential tremor 1
Drosophila melanogaster (fruit fly)
DOID:480
  • movement disease
Drosophila melanogaster (fruit fly)
DOID:0112143
  • retinitis pigmentosa 86
  • Aliases:
    • RP86
Mus musculus (house mouse)
DOID:1229
  • paranoid schizophrenia
  • Aliases:
    • Paranoid type schizophrenia
    • Paraphrenia - late
    • Paraphrenic schizophrenia
    • chronic paranoid schizophrenia
    • paranoid type schizophrenia subchronic state
Homo sapiens (human)
DOID:9651
  • systolic heart failure
Homo sapiens (human)
DOID:0080784
  • urinary tract infection
  • Aliases:
    • UTI
Homo sapiens (human)
DOID:0080205
  • CAKUT
  • Aliases:
    • Congenital anomalies of the kidney and urinary tract
    • Renal or urinary tract malformation
Homo sapiens (human)
DOID:0110574
  • autosomal dominant nonsyndromic deafness 4B
  • Aliases:
    • DFNA4B
    • autosomal dominant deafness 4B
Mus musculus (house mouse)
DOID:0110573
  • autosomal dominant nonsyndromic deafness 4A
  • Aliases:
    • DFNA4A
    • autosomal dominant deafness 4A
Mus musculus (house mouse)
DOID:0111636
  • autosomal recessive nonsyndromic deafness 113
  • Aliases:
    • DFNB113
    • autosomal recessive deafness 113
Mus musculus (house mouse)
DOID:14504
  • Niemann-Pick disease
  • Aliases:
    • Sphingomyelinase Deficiency Disease
    • lipoid histiocytosis
    • sphingomyelin lipidosis
Drosophila melanogaster (fruit fly)
DOID:0070113
  • Niemann-Pick disease type C1
  • Aliases:
    • NPC1
Drosophila melanogaster (fruit fly)
DOID:0080572
  • congenital disorder of glycosylation Iw
  • Aliases:
    • congenital disorder of glycosylation 1w
Drosophila melanogaster (fruit fly)
DOID:0080697
  • Opitz GBBB syndrome
  • Aliases:
    • Opitz G/BBB Syndrome
    • Opitz GBBB syndrome type I
Mus musculus (house mouse)
DOID:0110225
  • Brugada syndrome 8
  • Aliases:
    • BRGDA8
Mus musculus (house mouse)
DOID:0060706
  • X-linked lymphoproliferative syndrome 2
  • Aliases:
    • XIAP deficiency
    • XLP2
Homo sapiens (human)
DOID:0060335
  • autosomal dominant sideroblastic anemia 4
Homo sapiens (human)
DOID:0112056
  • X-linked intellectual disability-short stature-overweight syndrome
  • Aliases:
    • MRX12
    • MRX35
    • X-linked mental retardation 12
    • X-linked mental retardation 35
Mus musculus (house mouse)
DOID:0112022
  • non-syndromic X-linked intellectual disability 21
  • Aliases:
    • MRX21
    • MRX34
    • X-linked mental retardation 21
    • X-linked mental retardation 21/34
    • X-linked mental retardation 34
Mus musculus (house mouse)
DOID:0110163
  • Charcot-Marie-Tooth disease axonal type 2F
  • Aliases:
    • CMT2F
    • Charcot-Marie-Tooth neuronal type 2F
    • Charcot-Marie-Tooth neuropathy type 2F
    • autosomal dominant Charcot-Marie-Tooth disease type 2F
Homo sapiens (human)
DOID:0111207
  • autosomal dominant distal hereditary motor neuronopathy 3
  • Aliases:
    • HMN IIB
    • HMN2B
    • distal hereditary motor neuronopathy type 2B
    • distal hereditary motor neuropathy type IIB
Homo sapiens (human)
DOID:0090084
  • hypogonadotropic hypogonadism 5 with or without anosmia
Drosophila melanogaster (fruit fly)
DOID:0050338
  • primary bacterial infectious disease
Drosophila melanogaster (fruit fly)
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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