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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 14026 - 14050 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Organism Source
DOID:0080254
  • orofaciodigital syndrome XVI
Rattus norvegicus (Norway rat)
DOID:0110705
  • hypotrichosis 8
  • Aliases:
    • Hypt8
    • Lah3
    • hypotrichosis, localized, autosomal recessive 3
Rattus norvegicus (Norway rat)
DOID:0060614
  • ulnar-mammary syndrome
  • Aliases:
    • Pallister ulnar-mammary syndrome
    • Schinzel syndrome
Homo sapiens (human)
DOID:0111102
  • maturity-onset diabetes of the young type 3
  • Aliases:
    • MODY type 3
    • MODY3
Homo sapiens (human)
DOID:4471
  • chromophobe renal cell carcinoma
  • Aliases:
    • Chromophobe carcinoma of kidney
    • chromophobe adenocarcinoma
    • kidney chromophobe
    • renal cell carcinoma, chromophobe cell
Homo sapiens (human)
DOID:0110757
  • type 1 diabetes mellitus 20
  • Aliases:
    • IDDM20
    • Insulin-Dependent Diabetes Mellitus 20
Homo sapiens (human)
DOID:0111366
  • familial hepatic adenoma
  • Aliases:
    • familial liver cell adenomas
Homo sapiens (human)
DOID:0081143
  • agammaglobulinemia 8B
Homo sapiens (human)
DOID:0081140
  • agammaglobulinemia 8A
Homo sapiens (human)
DOID:0110857
  • posterior polymorphous corneal dystrophy 3
  • Aliases:
    • Ppcd3
Homo sapiens (human)
DOID:0090070
  • hypogonadotropic hypogonadism
  • Aliases:
    • congenital idiopathic hypogonadotropic hypogonadism
    • hypogonadotropism
    • isolated congenital gonadotropin deficiency
Homo sapiens (human)
DOID:0080354
  • Phelan-McDermid syndrome
  • Aliases:
    • 22q13.3 deletion syndrome
    • monosomy 22q13 syndrome
Homo sapiens (human)
DOID:0060835
  • isolated microphthalmia 6
  • Aliases:
    • MCOP6
    • posterior nonsyndromic microphthalmia
Mus musculus (house mouse)
DOID:2908
  • Treacher Collins syndrome
  • Aliases:
    • Franceschetti syndrome
    • mandibulofacial dysostosis
Homo sapiens (human)
DOID:0080789
  • Treacher Collins syndrome 1
Homo sapiens (human)
DOID:14179
  • X-linked agammaglobulinemia
  • Aliases:
    • BTK deficiency
    • Bruton agammaglobulinemia tyrosine kinase deficiency
    • Bruton disease
    • Bruton's Sex-Linked Agammaglobulinemia
    • Bruton's agammaglobulinaemia
    • Bruton's type agammaglobulinemia
    • Bruton-type agammaglobulinemia
Homo sapiens (human)
DOID:0060875
  • isolated growth hormone deficiency type III
  • Aliases:
    • Fleisher syndrome
    • IGHD III
    • X-linked IGHD
    • X-linked agammaglobulinemia and isolated growth hormone deficiency
    • X-linked hypogammaglobulinemia and isolated growth hormone deficiency
    • X-linked isolated growth hormone deficiency
    • congenital IGHD type III
    • congenital isolated GH deficiency type III
    • congenital isolated growth hormone deficiency type III
    • growth hormone deficiency with hypogammaglobulinemia
Homo sapiens (human)
DOID:0112249
  • GAPO syndrome
  • Aliases:
    • growth delay-alopecia-pseudoanodontia-optic atrophy syndrome
Mus musculus (house mouse)
DOID:0112247
  • congenital heart defects, dysmorphic facial features, and intellectual developmental disorder
  • Aliases:
    • CDK13-Related CHDFIDD
    • CDK13-Related Disorder
    • CHDFIDD
Mus musculus (house mouse)
DOID:0111027
  • hemochromatosis type 2A
  • Aliases:
    • HFE2A
Mus musculus (house mouse)
DOID:0080840
  • optic atrophy 12
Mus musculus (house mouse)
DOID:0050952
  • spastic ataxia
Mus musculus (house mouse)
DOID:0050977
  • spinocerebellar ataxia type 28
Mus musculus (house mouse)
DOID:0050944
  • spastic ataxia 5
Mus musculus (house mouse)
DOID:0060438
  • Cole-Carpenter syndrome
Mus musculus (house mouse)
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Last updated: December 9, 2024