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 11051 - 11075 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Organism Source
DOID:1591
  • renovascular hypertension
Caenorhabditis elegans
DOID:11830
  • myopia
  • Aliases:
    • near vision
    • near-sightedness
    • short-sightedness
Caenorhabditis elegans
DOID:9884
  • muscular dystrophy
Caenorhabditis elegans
DOID:0110539
  • autosomal recessive nonsyndromic deafness 97
  • Aliases:
    • DFNB97
    • autosomal recessive deafness 97
Mus musculus (house mouse)
DOID:4552
  • large cell carcinoma
Mus musculus (house mouse)
DOID:4465
  • papillary renal cell carcinoma
  • Aliases:
    • Chromophil carcinoma of kidney
    • papillary kidney carcinoma
    • sporadic papillary renal cell carcinoma
Mus musculus (house mouse)
DOID:0050476
  • Barth syndrome
  • Aliases:
    • 3-methylglutaconicaciduria type 2
    • 3-methylglutaconicaciduria type II
    • MGA Type 2
    • MGA type II
Mus musculus (house mouse)
DOID:2280
  • hidradenitis suppurativa
  • Aliases:
    • Acne inversa, familial
Caenorhabditis elegans
DOID:8552
  • chronic myeloid leukemia
  • Aliases:
    • CML
    • CML - chronic Myelogenous Leukemia
    • Myeloid Leukemia, chronic
    • chronic granulocytic leukaemia
    • chronic granulocytic leukemia
    • chronic myelogenous leukaemia
    • chronic myelogenous leukemia
    • chronic myeloid leukaemia
Caenorhabditis elegans
DOID:11054
  • urinary bladder cancer
  • Aliases:
    • bladder cancer
    • tumor of the bladder
Caenorhabditis elegans
DOID:0110541
  • autosomal dominant nonsyndromic deafness 1
  • Aliases:
    • DFNA1
    • Konigsmark syndrome
    • LFHL1
    • autosomal dominant deafness 1
    • autosomal dominant deafness 1, with or without thrombocytopenia
    • hereditary low frequency hearing loss 1
Homo sapiens (human)
DOID:0060690
  • autosomal dominant auditory neuropathy 1
  • Aliases:
    • AUNA1
    • NSDAN
    • nonsyndromic dominant auditory neuropathy
Homo sapiens (human)
DOID:0110367
  • retinitis pigmentosa 38
  • Aliases:
    • RP38
Mus musculus (house mouse)
DOID:0080079
  • nonsyndromic congenital nail disorder 1
  • Aliases:
    • nonsyndromic congenital nail disorder 10
    • twenty-nail dystrophy
Caenorhabditis elegans
DOID:0080845
  • omodysplasia 2
Caenorhabditis elegans
DOID:1928
  • Williams-Beuren syndrome
  • Aliases:
    • Fanconi Schlesinger syndrome
    • WBS
Caenorhabditis elegans
DOID:2154
  • nephroblastoma
  • Aliases:
    • adult nephroblastoma
Caenorhabditis elegans
DOID:3459
  • breast carcinoma
  • Aliases:
    • Mammary carcinoma
    • carcinoma of breast
Caenorhabditis elegans
DOID:127
  • leiomyoma
  • Aliases:
    • leiomyomatous neoplasm
    • leiomyomatous tumor
Caenorhabditis elegans
DOID:0050563
  • nonsyndromic deafness
  • Aliases:
    • nonsyndromic hearing loss
    • nonsyndromic hereditary hearing loss
Caenorhabditis elegans
DOID:0110645
  • long QT syndrome 2
  • Aliases:
    • LQT2
Caenorhabditis elegans
DOID:0050814
  • temtamy preaxial brachydactyly syndrome
  • Aliases:
    • PREAXIAL BRACHYDACTYLY SYNDROME, TEMTAMY TYPE
Caenorhabditis elegans
DOID:14365
  • systemic primary carnitine deficiency disease
  • Aliases:
    • carnitine transporter deficiency
    • carnitine uptake defect
    • deficiency of plasma-membrane carnitine transporter
    • primary carnitine deficiency
    • renal carnitine transport defect
Caenorhabditis elegans
DOID:1920
  • hyperuricemia
  • Aliases:
    • Blood urate raized
    • uricacidemia
Caenorhabditis elegans
DOID:1852
  • intrahepatic cholestasis
  • Aliases:
    • neonatal intrahepatic cholestasis
Caenorhabditis elegans

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Last updated: December 9, 2024