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 1201 - 1225 of 4621 in total
Disease ID Disease Name ▼ Gene Symbol Gene ID Organism
DOID:440
  • neuromuscular disease
Homo sapiens (human)
DOID:2001
  • neuroma
Homo sapiens (human)
DOID:14464
  • neuroleptic malignant syndrome
Homo sapiens (human)
DOID:12388
  • neurohypophyseal diabetes insipidus
  • Aliases:
    • Pituitary diabetes insipidus
    • Vasopressin deficiency
    • vasopressin defective diabetes insipidus
Homo sapiens (human)
DOID:12143
  • neurogenic bladder
  • Aliases:
    • Neuropathic bladder
    • neurogenic dysfunction of the urinary bladder
    • neurogenic urinary bladder disorder
Homo sapiens (human)
DOID:14286
  • neurogenic arthropathy
  • Aliases:
    • Arthropathy associated with neurological disorder
    • Charcot's arthropathy
    • Neuropathic arthropathy
Homo sapiens (human)
DOID:3512
  • neurofibrosarcoma
  • Aliases:
    • Neurosarcoma
Homo sapiens (human)
DOID:8712
  • neurofibromatosis
Homo sapiens (human)
DOID:0111253
  • neurofibromatosis 1
  • Aliases:
    • NF1
    • Peripheral Neurofibromatosis
    • Recklinghausen's neurofibromatosis
    • neurofibromatosis type I
    • von Recklinghausen Disease
Homo sapiens (human)
DOID:962
  • neurofibroma
Homo sapiens (human)
DOID:169
  • neuroendocrine tumor
  • Aliases:
    • neuroendocrine neoplasm
Homo sapiens (human)
DOID:1800
  • neuroendocrine carcinoma
Homo sapiens (human)
DOID:171
  • neuroectodermal tumor
  • Aliases:
    • primitive Neuroectodermal neoplasm
Homo sapiens (human)
DOID:1289
  • neurodegenerative disease
  • Aliases:
    • degenerative disease
Homo sapiens (human)
DOID:0110734
  • neurodegeneration with brain iron accumulation
  • Aliases:
    • NBIA
Homo sapiens (human)
DOID:0110740
  • neurodegeneration with brain iron accumulation 6
  • Aliases:
    • CoPAN
    • NBIA6
    • Neurodegeneration with brain iron accumulation due to COASY mutation
Homo sapiens (human)
DOID:0110739
  • neurodegeneration with brain iron accumulation 5
  • Aliases:
    • BPAN
    • Beta-Propeller Protein-Associated Neurodegeneration
    • NBIA5
    • SENDA
    • Static Encephalopathy Of Childhood With Neurodegeneration In Adulthood
Homo sapiens (human)
DOID:0110738
  • neurodegeneration with brain iron accumulation 4
  • Aliases:
    • MPAN
    • Mitochondrial Protein-Associated Neurodegeneration
    • NBIA due to C19orf12 mutation
    • NBIA4
    • Neurodegeneration with brain iron accumulation due to C19orf12 mutation
    • Neurodegeneration with brain iron accumulation type 4
Homo sapiens (human)
DOID:0110737
  • neurodegeneration with brain iron accumulation 3
  • Aliases:
    • Adult basal ganglia disease
    • Ferritin-related neurodegeneration
    • Hereditary ferritinopathy
    • NBIA3
    • Neuroferritinopathy
    • Neuroferritinopathy; Basal Ganglia Disease, Adult-Onset
Homo sapiens (human)
DOID:0110736
  • neurodegeneration with brain iron accumulation 2b
  • Aliases:
    • NBIA2b
    • Neuroaxonal Dystrophy, Atypical
    • Neurodegeneration With Brain Iron Accumulation, Pla2g6-Related
Homo sapiens (human)
DOID:0110735
  • neurodegeneration with brain iron accumulation 2a
  • Aliases:
    • INAD1
    • Infantile Neuroaxonal Dystrophy 1
    • NBIA2a
    • Neurodegeneration, Pla2g6-Associated
    • Seitelberger Disease
Homo sapiens (human)
DOID:11569
  • neurocirculatory asthenia
  • Aliases:
    • Cardiovascular malfunction arising from mental factors
    • Cardiovascular neurosis
    • Da Costa's syndrome
    • Krishaber's disease
Homo sapiens (human)
DOID:769
  • neuroblastoma
Homo sapiens (human)
DOID:2367
  • neuroaxonal dystrophy
Homo sapiens (human)
DOID:0050765
  • neuroacanthocytosis
Homo sapiens (human)

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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: August 19, 2024