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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 12501 - 12525 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Organism Source
DOID:1579
  • respiratory system disease
Mus musculus (house mouse)
DOID:0081030
  • central conducting lymphatic anomaly
  • Aliases:
    • lymphatic malformation-7
Mus musculus (house mouse)
DOID:75
  • lymphatic system disease
  • Aliases:
    • Lymphangiopathy
    • Lymphatic disease
    • disease of lympoid system
    • disorder of lymph node and lymphatics
    • disorder of lymphatic system
    • disorder of lymphoid system
    • lymphatic disorder
    • lympoid system disease
Mus musculus (house mouse)
DOID:264
  • hemangiopericytoma
  • Aliases:
    • Haemangiopericytic meningioma
    • hemangiopericytoma, malignant
    • malignant hemangiopericytoma
Mus musculus (house mouse)
DOID:0110734
  • neurodegeneration with brain iron accumulation
  • Aliases:
    • NBIA
Homo sapiens (human)
DOID:0110229
  • cataract 6 multiple types
  • Aliases:
    • CTRCT6
Mus musculus (house mouse)
DOID:0070041
  • autosomal dominant intellectual developmental disorder 11
  • Aliases:
    • MRD11
    • autosomal dominant mental retardation 11
    • autosomal dominant non-syndromic intellectual disability 11
Mus musculus (house mouse)
DOID:1800
  • neuroendocrine carcinoma
Mus musculus (house mouse)
DOID:12783
  • migraine without aura
  • Aliases:
    • common migraine
Mus musculus (house mouse)
DOID:0110389
  • retinitis pigmentosa 73
  • Aliases:
    • RP73
Homo sapiens (human)
DOID:0111393
  • mucopolysaccharidosis type IIIC
  • Aliases:
    • Acetyl-CoA alpha-glucosaminide acetyltransferase deficiency
    • HGSNAT deficiency
    • Heparan-alpha-glucosaminide N-acetyltransferase deficiency
    • MPS3C
    • MPSIIIC
    • Mucopolysaccharidosis type 3C
    • Sanfilippo syndrome type C
    • mucopolysaccharidosis type IIIC (Sanfilippo C)
Homo sapiens (human)
DOID:12801
  • mucopolysaccharidosis III
  • Aliases:
    • Mucopolysaccharidosis, MPS-III
    • N-sulphoglucosamine sulphohydrolase deficiency
    • Sanfilippo's syndrome
    • heparan sulfate sulfatase deficiency
Homo sapiens (human)
DOID:1037
  • lymphoid leukemia
  • Aliases:
    • lymphoblastic leukaemia
    • lymphoblastic leukemia
    • lymphocytic leukaemia
Mus musculus (house mouse)
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
Mus musculus (house mouse)
DOID:0110052
  • amelogenesis imperfecta type 1B
  • Aliases:
    • AI1B
    • AIH2
    • amelogenesis imperfecta type IB
    • autosomal dominant hypoplastic local amelogenesis imperfecta
    • hereditary localized enamel hypoplasia
Mus musculus (house mouse)
DOID:0081150
  • common variable immunodeficiency 7
Homo sapiens (human)
DOID:0050460
  • Wolf-Hirschhorn syndrome
  • Aliases:
    • 4p deletion syndrome
    • PITT SYNDROME
    • Pitt-Rogers-Danks Syndrome
    • chromosome 4p16.3 deletion syndrome
Homo sapiens (human)
DOID:0110436
  • dilated cardiomyopathy 1L
  • Aliases:
    • CMD1L
Homo sapiens (human)
DOID:936
  • brain disease
  • Aliases:
    • encephalopathy
Homo sapiens (human)
DOID:0110805
  • hereditary spastic paraplegia 53
  • Aliases:
    • SPG53
    • autosomal recessive spastic paraplegia 53
    • autosomal recessive spastic paraplegia type 53
Homo sapiens (human)
DOID:0090129
  • carnitine palmitoyltransferase I deficiency
  • Aliases:
    • CPT I deficiency
    • CPT1A deficiency
    • L-CPT1 deficiency
    • carnitine palmitoyl transferase 1A deficiency
    • carnitine palmitoyl transferase IA deficiency
    • hepatic CPT deficiency type I
    • hepatic carnitine palmitoyl transferase 1 deficiency
    • hepatic carnitine palmitoyl transferase I deficiency
Homo sapiens (human)
DOID:3319
  • lymphangioleiomyomatosis
  • Aliases:
    • lung lymphangioleiomyomatosis
    • lymphangiomyomatosis
    • pulmonary lymphangioleiomyomatosis
Homo sapiens (human)
DOID:3146
  • lipid metabolism disorder
  • Aliases:
    • dyslipidemia
    • fatty acid metabolism disorder
Homo sapiens (human)
DOID:0080386
  • nephrotic syndrome type 10
Mus musculus (house mouse)
DOID:9280
  • carbamoyl phosphate synthetase I deficiency disease
  • Aliases:
    • CPS I deficiency
Homo sapiens (human)
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Last updated: December 9, 2024