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 2676 - 2700 of 4621 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲
DOID:1039
  • prolymphocytic leukemia
  • Aliases:
    • PLL
    • Prolymphocytic leukaemia
Homo sapiens (human)
DOID:3368
  • Ewing sarcoma of bone
  • Aliases:
    • Ewing's sarcoma/bone peripheral primitive neuroectodermal tumor
    • bone Ewing sarcoma
    • bone localized Ewing sarcoma
    • bone localized Ewing's sarcoma
    • localized Skeletal Ewing's sarcoma
Homo sapiens (human)
DOID:0070118
  • Meckel syndrome 4
  • Aliases:
    • MKS4
    • Meckel-Gruber syndrome, type 4
Homo sapiens (human)
DOID:3742
  • bladder squamous cell carcinoma
  • Aliases:
    • Epidermoid carcinoma of the urinary bladder
    • squamous cell carcinoma of bladder
Homo sapiens (human)
DOID:0060485
  • Mowat-Wilson syndrome
  • Aliases:
    • Hirschsprung disease mental retardation syndrome
    • microcephaly, mental retardation, and distinct facial featrues, with or without Hirschprung disease
Homo sapiens (human)
DOID:10573
  • osteomalacia
Homo sapiens (human)
DOID:2048
  • autoimmune hepatitis
  • Aliases:
    • Autoimmune chronic active hepatitis
    • autoimmune hepatitis with centrilobular necrosis
Homo sapiens (human)
DOID:0110436
  • dilated cardiomyopathy 1L
  • Aliases:
    • CMD1L
Homo sapiens (human)
DOID:2766
  • ethmoid sinus adenocarcinoma
  • Aliases:
    • adenocarcinoma of the ethmoid sinus
Homo sapiens (human)
DOID:0080094
  • myofibrillar myopathy 3
  • Aliases:
    • LGMD 1A
    • autosomal dominant limb-girdle muscular dystrophy type 1A
    • myotilinopathy
    • spheroid body myopathy
Homo sapiens (human)
DOID:13014
  • shipyard eye
  • Aliases:
    • EKC
    • Epidemic keratoconjunctivitis
Homo sapiens (human)
DOID:0111277
  • mitochondrial trifunctional protein deficiency
  • Aliases:
    • MTPD
    • TFP deficiency
    • TFPD
Homo sapiens (human)
DOID:0050441
  • mucosulfatidosis
  • Aliases:
    • Sulfatidosis, Juvenile, Austin Type
    • multiple sulfatase deficiency disease
Homo sapiens (human)
DOID:9893
  • periodontosis
Homo sapiens (human)
DOID:0080197
  • congenital muscular dystrophy with cataracts and intellectual disability
Homo sapiens (human)
DOID:12705
  • Friedreich ataxia
  • Aliases:
    • Friedreich's ataxia
    • Friedreich's tabes
Homo sapiens (human)
DOID:0060790
  • hypomyelinating leukodystrophy 3
  • Aliases:
    • HLD3
    • Pelizaeus-Merzbacher-like disease due to AIMP1 mutation
Homo sapiens (human)
DOID:14464
  • neuroleptic malignant syndrome
Homo sapiens (human)
DOID:676
  • juvenile rheumatoid arthritis
  • Aliases:
    • Pauciarticular onset juvenile chronic arthritis
    • Still's disease
    • acute juvenile rheumatoid arthritis
    • juvenile chronic polyarthritis
    • juvenile idiopathic arthritis
    • monarticular juvenile rheumatoid arthritis
    • pauciarticular juvenile arthritis
    • systemic juvenile rheumatoid arthritis
Homo sapiens (human)
DOID:0080567
  • congenital disorder of glycosylation Ip
  • Aliases:
    • congenital disorder of glycosylation 1p
Homo sapiens (human)
DOID:0110447
  • dilated cardiomyopathy 1DD
  • Aliases:
    • CMD1DD
Homo sapiens (human)
DOID:5016
  • hepatocellular clear cell carcinoma
  • Aliases:
    • Clear cell carcinoma of the Liver cells
    • Hepatocellular carcinoma, clear cell type
Homo sapiens (human)
DOID:731
  • urinary system benign neoplasm
  • Aliases:
    • neoplasm of urinary system
    • tumor of the urinary system
    • tumor of urinary tract
    • urinary tract neoplasm
Homo sapiens (human)
DOID:0110148
  • Charcot-Marie-Tooth disease type 1A
  • Aliases:
    • CMT1A
    • Charcot-Marie-Tooth neuropathy type 1A
    • HMSN1A
    • autosomal dominant Charcot-Marie-Tooth disease with focally folded myelin sheaths type 1A
    • hereditary motor and sensory neuropathy 1A
    • microduplication 17p12
Homo sapiens (human)
DOID:0060359
  • Sakati-Nyhan syndrome
  • Aliases:
    • ACPS with leg hypoplasia
    • Sakati syndrome
    • Sakati-Nyhan-Tisdale syndrome
    • acrocephalopolysyndactyly Type III
    • acrocephalopolysyndactyly type 3
Homo sapiens (human)

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Last updated: August 19, 2024