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:0111909
  • autosomal dominant thrombophilia due to protein C deficiency
  • Aliases:
    • THPH3
    • autosomal dominant PROC deficiency
    • autosomal dominant protein C deficiency
Rattus norvegicus (Norway rat)
DOID:3756
  • protein C deficiency
Rattus norvegicus (Norway rat)
DOID:0111904
  • autosomal recessive thrombophilia due to protein C deficiency
  • Aliases:
    • THPH4
    • autosomal recessive PROC deficiency
    • autosomal recessive protein C deficiency
Rattus norvegicus (Norway rat)
DOID:0111902
  • thrombophilia due to activated protein C resistance
  • Aliases:
    • APC resistance
    • PCCF deficiency
    • PROC cofactor deficiency
    • THPH2
    • activated protein C resistance
    • thrombophilia V
    • thrombophilia due to deficiency of activated protein C cofactor
Rattus norvegicus (Norway rat)
DOID:0090092
  • hypogonadotropic hypogonadism 3 with or without anosmia
Rattus norvegicus (Norway rat)
DOID:0090092
  • hypogonadotropic hypogonadism 3 with or without anosmia
Mus musculus (house mouse)
DOID:0110376
  • retinitis pigmentosa 41
  • Aliases:
    • RP41
Mus musculus (house mouse)
DOID:0111019
  • cone-rod dystrophy 12
  • Aliases:
    • CORD12
Mus musculus (house mouse)
DOID:0070517
  • retinal macular dystrophy 2
  • Aliases:
    • MCDR2
Mus musculus (house mouse)
DOID:2451
  • protein S deficiency
  • Aliases:
    • Protein S deficiency disease
Mus musculus (house mouse)
DOID:0111905
  • autosomal recessive thrombophilia due to protein S deficiency
  • Aliases:
    • THPH6
    • autosomal recessive thrombophilia due to congenital protein S deficiency
    • severe hereditary thrombophilia due to congenital protein S deficiency
Mus musculus (house mouse)
DOID:0111900
  • autosomal dominant thrombophilia due to protein S deficiency
  • Aliases:
    • THPH5
Mus musculus (house mouse)
DOID:0110403
  • retinitis pigmentosa 13
  • Aliases:
    • RP13
Mus musculus (house mouse)
DOID:9822
  • partial central choroid dystrophy
  • Aliases:
    • Choroidal dystrophy, central areolar
Mus musculus (house mouse)
DOID:0110383
  • retinitis pigmentosa 7
  • Aliases:
    • RP7
Mus musculus (house mouse)
DOID:0060863
  • patterned macular dystrophy
  • Aliases:
    • patterned dystrophy of retinal pigment epithelium
Mus musculus (house mouse)
DOID:0060866
  • patterned macular dystrophy 1
  • Aliases:
    • MDPT1
    • butterfly-shaped pigmentary maculary dystrophy 1
Mus musculus (house mouse)
DOID:11105
  • fundus albipunctatus
  • Aliases:
    • Pigmentary retinal dystrophy
    • retinitis punctata albescens
Rattus norvegicus (Norway rat)
DOID:0060866
  • patterned macular dystrophy 1
  • Aliases:
    • MDPT1
    • butterfly-shaped pigmentary maculary dystrophy 1
Rattus norvegicus (Norway rat)
DOID:0110383
  • retinitis pigmentosa 7
  • Aliases:
    • RP7
Rattus norvegicus (Norway rat)
DOID:9822
  • partial central choroid dystrophy
  • Aliases:
    • Choroidal dystrophy, central areolar
Rattus norvegicus (Norway rat)
DOID:0060863
  • patterned macular dystrophy
  • Aliases:
    • patterned dystrophy of retinal pigment epithelium
Rattus norvegicus (Norway rat)
DOID:0050647
  • Arts syndrome
  • Aliases:
    • ARTS
    • Lethal ataxia with deafness and optic atrophy
    • MRXS18
    • MRXSARTS
    • fatal X-linked ataxia with deafness and loss of vision
    • syndromic X-linked mental retardation 18
    • syndromic X-linked mental retardation Arts type
Mus musculus (house mouse)
DOID:0110210
  • Charcot-Marie-Tooth disease X-linked recessive 5
  • Aliases:
    • CMT5X
    • CMTX5
    • Charcot-Marie-Tooth neuropathy X-linked recessive 5
    • Rosenberg-Chutorian syndrome
    • X-linked Charcot-Marie-Tooth disease type 5
    • optic atrophy, polyneuropathy, and deafness
Mus musculus (house mouse)
DOID:0111739
  • X-linked deafness 1
  • Aliases:
    • DFN2
    • DFNX1
    • X-linked sensorineural congenital deafness 2
Mus musculus (house mouse)

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Last updated: December 9, 2024