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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 6726 - 6750 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:18
  • urinary system disease
  • Aliases:
    • Non-neoplastic urinary tract disease
    • urinary tract disease
Homo sapiens (human)
DOID:9296
  • cleft lip
  • Aliases:
    • Labium leporinum
    • cheiloschisis
    • cleft lip, unilateral, complete
    • complete unilateral cleft lip
    • hare lip
Caenorhabditis elegans
DOID:0111312
  • idiopathic generalized epilepsy 11
  • Aliases:
    • EIG11
Mus musculus (house mouse)
DOID:0060967
  • dystonia 22, adult-onset
Mus musculus (house mouse)
DOID:0080664
  • diaphyseal medullary stenosis with malignant fibrous histiocytoma
  • Aliases:
    • Hardcastle syndrome
    • bone dysplasia-medullary fibrosarcoma syndrome
    • diaphyseal medullary stenosis-malignant fibrous histiocytoma syndrome
Saccharomyces cerevisiae S288C
DOID:0060242
  • synpolydactyly
  • Aliases:
    • syndactyly type 2
Homo sapiens (human)
DOID:0110771
  • hereditary spastic paraplegia 18
  • Aliases:
    • IDMDC
    • SPG18
    • autosomal recessive spastic paraplegia 18
    • autosomal recessive spastic paraplegia type 18
    • intellectual disability, motor dysfunction and joint contractures
Mus musculus (house mouse)
DOID:0060318
  • acute promyelocytic leukemia
  • Aliases:
    • acute myeloblastic leukaemia type 3
    • acute myeloblastic leukemia type 3
    • acute myeloid leukaemia M3
    • acute myeloid leukemia M3
    • acute promyelocytic leukaemia
Homo sapiens (human)
DOID:11758
  • iron deficiency anemia
Xenopus tropicalis (tropical clawed frog)
DOID:0112051
  • non-syndromic X-linked intellectual disability 30
  • Aliases:
    • MRX30
    • MRX47
    • X-linked mental retardation 30
    • X-linked mental retardation 30/47
    • X-linked mental retardation 47
Mus musculus (house mouse)
DOID:0080266
  • primary ciliary dyskinesia 37
Homo sapiens (human)
DOID:2476
  • hereditary spastic paraplegia
  • Aliases:
    • French settlement disease
    • Strumpell-Lorrain disease
    • familial spastic paraplegia
    • hereditary spastic paraparesis
Saccharomyces cerevisiae S288C
DOID:0111238
  • congenital muscular dystrophy-dystroglycanopathy type A13
  • Aliases:
    • MDDGA13
    • Walker-Warburg syndrome or muscle-eye-brain disease, B3GNT1-related
    • Walker-Warburg syndrome or muscle-eye-brain disease, B4GNT1-related
    • congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A13
Danio rerio (zebrafish)
DOID:13270
  • erythropoietic protoporphyria
  • Aliases:
    • EPP
    • Protoporphyria
Mus musculus (house mouse)
DOID:3443
  • mammary Paget's disease
  • Aliases:
    • Paget cell neoplasm
    • Paget's disease
    • Paget's disease of the breast
    • mammary Paget disease
Mus musculus (house mouse)
DOID:12894
  • Sjogren's syndrome
  • Aliases:
    • Sicca syndrome
    • Sjogren syndrome
    • xerodermosteosis
Rattus norvegicus (Norway rat)
DOID:0080351
  • CLOVES syndrome
  • Aliases:
    • congenital lipomatous overgrowth, vascular malformations, and epidermal nevi
Mus musculus (house mouse)
DOID:0110741
  • type 1 diabetes mellitus 2
  • Aliases:
    • IDDM2
    • Insulin-Dependent Diabetes Mellitus 2
Danio rerio (zebrafish)
DOID:5844
  • myocardial infarction
  • Aliases:
    • Myocardial infarct
    • heart attack
Xenopus tropicalis (tropical clawed frog)
DOID:9471
  • meningitis
Mus musculus (house mouse)
DOID:4752
  • multiple system atrophy
  • Aliases:
    • Shy-Drager syndrome
Caenorhabditis elegans
DOID:5409
  • lung small cell carcinoma
Danio rerio (zebrafish)
DOID:0060198
  • amyotrophic lateral sclerosis type 6
  • Aliases:
    • ALS6
    • amyotrophic lateral sclerosis 6, with or without frontotemporal dementia
    • autosomal recessive amyotrophic lateral sclerosis 6
Mus musculus (house mouse)
DOID:1074
  • kidney failure
  • Aliases:
    • renal failure
Homo sapiens (human)
DOID:0111248
  • cerebrocostomandibular syndrome
  • Aliases:
    • CCM syndrome
    • CCMS
    • cerebro-costo-mandibular syndrome
    • rib gap defects with micrognathia
Homo sapiens (human)
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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