GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB), DisGeNET, and Alliance of Genome Resources is integrated into one list.

Source Last Updated
Alliance of Genome Resources July 29, 2024
DisGeNET July 29, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 4126 - 4150 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲
DOID:1229
  • paranoid schizophrenia
  • Aliases:
    • Paranoid type schizophrenia
    • Paraphrenia - late
    • Paraphrenic schizophrenia
    • chronic paranoid schizophrenia
    • paranoid type schizophrenia subchronic state
Homo sapiens (human)
DOID:0110056
  • amelogenesis imperfecta type 1C
  • Aliases:
    • AI1C
    • amelogenesis imperfecta type IC
    • autosomal recessive amelogenesis imperfecta hypoplastic with or without openbite malocclusion
    • autosomal recessive amelogenesis imperfecta local hypoplastic type
Homo sapiens (human)
DOID:5940
  • malignant peripheral nerve sheath tumor
  • Aliases:
    • malignant neoplasm of the peripheral nerve Sheath
Homo sapiens (human)
DOID:0050778
  • Meckel syndrome
  • Aliases:
    • Meckel-Gruber syndrome
Homo sapiens (human)
DOID:0110729
  • neuronal ceroid lipofuscinosis 6A
  • Aliases:
    • CLN6
    • neuronal ceroid lipofuscinosis 6
    • neuronal ceroid lipofuscinosis 6 variable age of onset
Homo sapiens (human)
DOID:0050441
  • mucosulfatidosis
  • Aliases:
    • Sulfatidosis, Juvenile, Austin Type
    • multiple sulfatase deficiency disease
Homo sapiens (human)
DOID:3596
  • placental site trophoblastic tumor
  • Aliases:
    • Placental-Site Gestational Trophoblastic neoplasm
    • placental site trophoblastic tumour
Homo sapiens (human)
DOID:0050145
  • adenoiditis
  • Aliases:
    • chronic adenoiditis
Homo sapiens (human)
DOID:0090141
  • cortisone reductase deficiency 1
  • Aliases:
    • CORTRD1
Homo sapiens (human)
DOID:1595
  • melancholic depression
  • Aliases:
    • endogenous depression
    • major depressive disorder with melancholic features
    • melancholia
Homo sapiens (human)
DOID:10323
  • byssinosis
  • Aliases:
    • Flax-dressers' disease
    • Stripper's asthma
    • cotton mill fever
Homo sapiens (human)
DOID:0111619
  • combined D-2- and L-2-hydroxyglutaric aciduria
  • Aliases:
    • D,L-2-HGA
    • D,L-2-hydroxyglutaric acidemia
    • D,L-2-hydroxyglutaric aciduria
    • combined D,L-2-hydroxyglutaric aciduria
    • combined D-2-hydroxyglutaric acidemia and L-2-hydroxyglutaric acidemia
    • combined D-2-hydroxyglutaric aciduria and L-2-hydroxyglutaric aciduria
Homo sapiens (human)
DOID:14188
  • frozen shoulder
  • Aliases:
    • Adhesive capsulitis of shoulder
    • adhesions-capsulitis,shoulder
Homo sapiens (human)
DOID:4971
  • myelofibrosis
  • Aliases:
    • Agnogenic myeloid metaplasia
    • Aleukemic myelosis
    • Megakaryocytic myelosclerosis
    • bone Marrow Fibrosis
    • myelosclerosis
    • primary myelofibrosis
Homo sapiens (human)
DOID:0110482
  • autosomal recessive nonsyndromic deafness 24
  • Aliases:
    • DFNB24
    • autosomal recessive deafness 24
Homo sapiens (human)
DOID:0110733
  • neuronal ceroid lipofuscinosis 9
  • Aliases:
    • CLN9
Homo sapiens (human)
DOID:65
  • connective tissue disease
  • Aliases:
    • connective tissue disorder
    • disorder of connective tissue
Homo sapiens (human)
DOID:0090048
  • dystonia 16
Homo sapiens (human)
DOID:11166
  • Human papillomavirus infectious disease
  • Aliases:
    • HPV
Homo sapiens (human)
DOID:0111898
  • CK syndrome
  • Aliases:
    • X-linked intellectual disability-microcephaly-cortical malformation-thin habitus syndrome
Homo sapiens (human)
DOID:0110574
  • autosomal dominant nonsyndromic deafness 4B
  • Aliases:
    • DFNA4B
    • autosomal dominant deafness 4B
Homo sapiens (human)
DOID:12721
  • multiple epiphyseal dysplasia
  • Aliases:
    • polyepiphyseal dysplasia
Homo sapiens (human)
DOID:5199
  • ureteral obstruction
Homo sapiens (human)
DOID:0060854
  • autosomal recessive pseudohypoaldosteronism type 1
  • Aliases:
    • PHA1B
    • autosomal recessive PHA 1
Homo sapiens (human)
DOID:0070118
  • Meckel syndrome 4
  • Aliases:
    • MKS4
    • Meckel-Gruber syndrome, type 4
Homo sapiens (human)

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Last updated: August 19, 2024