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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 4076 - 4100 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:0090030
  • corticosteroid-binding globulin deficiency
  • Aliases:
    • CBG deficiency
    • transcortin deficiency
Mus musculus (house mouse)
DOID:0110088
  • asphyxiating thoracic dystrophy 4
  • Aliases:
    • ATD4
    • SRTD4
    • short-rib thoracic dysplasia 4 with or without polydactyly
Mus musculus (house mouse)
DOID:0050770
  • polycystic liver disease
  • Aliases:
    • congenital cystic liver disease
    • congenital hepatic cyst
    • fibrocystic liver disease
Saccharomyces cerevisiae S288C
DOID:0050592
  • asphyxiating thoracic dystrophy
  • Aliases:
    • Jeune syndrome
    • short-rib thoracic dysplasia with or without polydactyly
    • thoracic pelvic phalangeal dystrophy
Mus musculus (house mouse)
DOID:0080297
  • Coffin-Siris syndrome 6
Homo sapiens (human)
DOID:0060738
  • junctional epidermolysis bullosa non-Herlitz type
  • Aliases:
    • GABEB
    • JEB-nH gen
    • JEN-nH
    • generalized atrophic benign epidermolysis bullosa
    • generalized junctional epidermolysis bullosa, non-Herlitz type
    • junctional epidermolysis bullosa generalisata mitis
    • junctional epidermolysis bullosa, Disentis type
Homo sapiens (human)
DOID:0111542
  • familial expansile osteolysis
  • Aliases:
    • FEO
    • McCabe disease
    • hereditary expansile polyostotic osteolytic dysplasia
Homo sapiens (human)
DOID:1700
  • X-linked ichthyosis
  • Aliases:
    • X-linked ichthyosis with steryl-sulphatase deficiency
    • X-linked placental steryl-sulphatase deficiency
    • X-linked recessive ichthyosis
Homo sapiens (human)
DOID:0111465
  • combined oxidative phosphorylation deficiency 21
  • Aliases:
    • COXPD21
Homo sapiens (human)
DOID:13884
  • sick sinus syndrome
  • Aliases:
    • sinus node infection
Mus musculus (house mouse)
DOID:0050579
  • glycogen storage disease XV
  • Aliases:
    • Glycogen storage disease 15
    • Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency
    • glycogen storage disease type XV
Danio rerio (zebrafish)
DOID:13129
  • severe pre-eclampsia
  • Aliases:
    • Severe pre-eclampsia, with delivery
    • antepartum severe pre-eclampsia
    • postpartum severe pre-eclampsia
    • severe preeclampsia
Caenorhabditis elegans
DOID:13481
  • thanatophoric dysplasia
Xenopus laevis (African clawed frog)
DOID:0110961
  • atypical Gaucher's disease due to saposin c deficiency
Homo sapiens (human)
DOID:0110875
  • holoprosencephaly 3
  • Aliases:
    • HLP3
    • HPE3
Caenorhabditis elegans
DOID:74
  • hematopoietic system disease
  • Aliases:
    • Blood disease
    • Blood dyscrasia
    • DISEASE OF THE BLOOD AND BLOOD-FORMING ORGANS
    • Hematological disease
    • blood disorder
    • disease of haematopoietic system
    • disease of hematopoietic system
    • haematopoietic system disease
Rattus norvegicus (Norway rat)
DOID:5593
  • gastric papillary adenocarcinoma
  • Aliases:
    • Papillary adenocarcinoma of stomach
Drosophila melanogaster (fruit fly)
DOID:14705
  • Pfeiffer syndrome
  • Aliases:
    • acrocephalosyndactylia type V
Xenopus tropicalis (tropical clawed frog)
DOID:14452
  • hypokalemic periodic paralysis
  • Aliases:
    • Hypokalemic familial periodic paralysis
    • Periodic paralysis I
    • Westphal disease
    • familial hypokalemic periodic paralysis
    • periodic hypokalemic paralysis
Rattus norvegicus (Norway rat)
DOID:1936
  • atherosclerosis
Rattus norvegicus (Norway rat)
DOID:10024
  • migraine with aura
  • Aliases:
    • classic migraine
Danio rerio (zebrafish)
DOID:10603
  • glucose intolerance
  • Aliases:
    • Glucose malabsorption
    • Malabsorption of glucose
Caenorhabditis elegans
DOID:11722
  • myotonic dystrophy type 1
  • Aliases:
    • Dystrophia myotonica
    • Steinert disease
    • congenital myotonic dystrophy
    • myotonic dystrophy of Steinert
Mus musculus (house mouse)
DOID:10584
  • retinitis pigmentosa
  • Aliases:
    • pericentral pigmentary retinopathy
Homo sapiens (human)
DOID:9775
  • diastolic heart failure
Rattus norvegicus (Norway rat)
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Last updated: December 9, 2024