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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 5776 - 5800 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:0080998
  • acute necrotizing pancreatitis
Rattus norvegicus (Norway rat)
DOID:0080732
  • Ehlers-Danlos syndrome classic-like 2
Rattus norvegicus (Norway rat)
DOID:0060887
  • ossification of the posterior longitudinal ligament of spine
  • Aliases:
    • OPLL
Drosophila melanogaster (fruit fly)
DOID:1949
  • cholecystitis
  • Aliases:
    • acute and chronic cholecystitis
    • acute cholecystitis
    • acute on chronic cholecystitis
    • chronic cholecystitis
Mus musculus (house mouse)
DOID:962
  • neurofibroma
Danio rerio (zebrafish)
DOID:8997
  • polycythemia vera
  • Aliases:
    • Osler-Vaquez syndrome
    • Polycythaemia rubra vera
    • Proliferative polycythaemia
    • chronic erythremia
Saccharomyces cerevisiae S288C
DOID:0080037
  • Worth syndrome
  • Aliases:
    • Worth's syndrome
    • autosomal dominant endosteal hyperostosis
    • autosomal dominant osteosclerosis
    • benign form of Worth hyperostosis corticalis generalisata with torus platinus
Mus musculus (house mouse)
DOID:0060540
  • Hermansky-Pudlak syndrome 2
Homo sapiens (human)
DOID:0112224
  • chondrodysplasia with joint dislocations gPAPP type
  • Aliases:
    • gPAPP deficiency
Rattus norvegicus (Norway rat)
DOID:14654
  • prostatitis
Rattus norvegicus (Norway rat)
DOID:0090129
  • carnitine palmitoyltransferase I deficiency
  • Aliases:
    • CPT I deficiency
    • CPT1A deficiency
    • L-CPT1 deficiency
    • carnitine palmitoyl transferase 1A deficiency
    • carnitine palmitoyl transferase IA deficiency
    • hepatic CPT deficiency type I
    • hepatic carnitine palmitoyl transferase 1 deficiency
    • hepatic carnitine palmitoyl transferase I deficiency
Mus musculus (house mouse)
DOID:2975
  • cystic kidney disease
  • Aliases:
    • renal Cyst
Rattus norvegicus (Norway rat)
DOID:767
  • muscular atrophy
  • Aliases:
    • Amyotrophia
    • Muscle wasting
    • Wasting - muscle
Drosophila melanogaster (fruit fly)
DOID:0110704
  • hypotrichosis 7
  • Aliases:
    • Hypt7
    • Lah2
    • hypotrichosis, localized, autosomal recessive 2
    • total Mari type hypotrichosis,
Homo sapiens (human)
DOID:0080181
  • PHARC syndrome
  • Aliases:
    • polyneyropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract
Danio rerio (zebrafish)
DOID:11206
  • opioid abuse
Drosophila melanogaster (fruit fly)
DOID:12783
  • migraine without aura
  • Aliases:
    • common migraine
Saccharomyces cerevisiae S288C
DOID:0060335
  • autosomal dominant sideroblastic anemia 4
Homo sapiens (human)
DOID:13812
  • adhesions of uterus
  • Aliases:
    • Band of uterus
    • Intrauterine adhesions
    • Intrauterine synechiae
Caenorhabditis elegans
DOID:0080212
  • polycystic kidney disease 4
Mus musculus (house mouse)
DOID:14069
  • cerebral malaria
  • Aliases:
    • Malarial encephalitis
Xenopus laevis (African clawed frog)
DOID:0112025
  • female-restricted syndromic X-linked intellectual disability 99
  • Aliases:
    • MRXS99F
    • X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability
    • female-restricted syndromic X-linked mental retardation 99
Mus musculus (house mouse)
DOID:0060748
  • familial temporal lobe epilepsy 1
  • Aliases:
    • ETL1
    • partial epilepsy with auditory features
Mus musculus (house mouse)
DOID:0070341
  • neonatal-onset type II citrullinemia
  • Aliases:
    • neonatal-onset type 2 citrullinemia
Homo sapiens (human)
DOID:0050782
  • Zollinger-Ellison 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