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 9326 - 9350 of 15957 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Organism Source
DOID:0070338
  • cerebellar hypoplasia
Mus musculus (house mouse)
DOID:3073
  • brain glioblastoma multiforme
  • Aliases:
    • Glioblastoma multiforme of brain
    • brain Glioblastoma
Rattus norvegicus (Norway rat)
DOID:0050933
  • ovarian serous carcinoma
Rattus norvegicus (Norway rat)
DOID:0050737
  • autosomal recessive disease
Mus musculus (house mouse)
DOID:0110868
  • congenital stationary night blindness 1D
  • Aliases:
    • CSNB1D
    • congenital stationary night blindness 1D autosomal recessive
Drosophila melanogaster (fruit fly)
DOID:11633
  • thyroid hormone resistance syndrome
  • Aliases:
    • Generalized thyroid hormone resistance
    • Refetoff syndrome
    • Thyroid hormone responsiveness defect
    • thyroid hormone resistance
Mus musculus (house mouse)
DOID:2280
  • hidradenitis suppurativa
  • Aliases:
    • Acne inversa, familial
Drosophila melanogaster (fruit fly)
DOID:0090070
  • hypogonadotropic hypogonadism
  • Aliases:
    • congenital idiopathic hypogonadotropic hypogonadism
    • hypogonadotropism
    • isolated congenital gonadotropin deficiency
Mus musculus (house mouse)
DOID:0081210
  • autosomal recessive intellectual developmental disorder 46
Mus musculus (house mouse)
DOID:11198
  • DiGeorge syndrome
  • Aliases:
    • 22q11.2 deletion syndrome
    • DiGeorge sequence
    • DiGeorge's syndrome
    • Pharyngeal pouch syndrome
Rattus norvegicus (Norway rat)
DOID:0081210
  • autosomal recessive intellectual developmental disorder 46
Rattus norvegicus (Norway rat)
DOID:0112069
  • nuclear type mitochondrial complex I deficiency 22
  • Aliases:
    • MC1DN22
Rattus norvegicus (Norway rat)
DOID:0112076
  • nuclear type mitochondrial complex I deficiency 13
  • Aliases:
    • MC1DN13
Mus musculus (house mouse)
DOID:0112086
  • nuclear type mitochondrial complex I deficiency 26
  • Aliases:
    • MC1DN26
Rattus norvegicus (Norway rat)
DOID:0112086
  • nuclear type mitochondrial complex I deficiency 26
  • Aliases:
    • MC1DN26
Mus musculus (house mouse)
DOID:0112075
  • nuclear type mitochondrial complex I deficiency 10
  • Aliases:
    • MC1DN10
Mus musculus (house mouse)
DOID:0112077
  • nuclear type mitochondrial complex I deficiency 15
  • Aliases:
    • MC1DN15
Rattus norvegicus (Norway rat)
DOID:0112139
  • nuclear type mitochondrial complex I deficiency 35
  • Aliases:
    • MC1DN35
Rattus norvegicus (Norway rat)
DOID:0112139
  • nuclear type mitochondrial complex I deficiency 35
  • Aliases:
    • MC1DN35
Mus musculus (house mouse)
DOID:0112098
  • nuclear type mitochondrial complex I deficiency 30
  • Aliases:
    • MC1DN30
Rattus norvegicus (Norway rat)
DOID:0111876
  • linear skin defects with multiple congenital anomalies 3
  • Aliases:
    • LSDMCA3
    • linear skin defects with cardiomyopathy and other congenital anomalies
Rattus norvegicus (Norway rat)
DOID:0112080
  • nuclear type mitochondrial complex I deficiency 32
  • Aliases:
    • MC1DN32
Mus musculus (house mouse)
DOID:0112079
  • nuclear type mitochondrial complex I deficiency 24
  • Aliases:
    • MC1DN24
Rattus norvegicus (Norway rat)
DOID:0112068
  • nuclear type mitochondrial complex I deficiency 5
  • Aliases:
    • MC1DN5
Mus musculus (house mouse)
DOID:0060536
  • mitochondrial complex I deficiency
  • Aliases:
    • isolated NADH-CoQ reductase deficiency
    • isolated NADH-coenzyme Q reductase deficiency
    • isolated NADH-ubiquinone reductase deficiency
    • isolated mitochondrial respiratory chain complex I deficiency
Rattus norvegicus (Norway rat)

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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