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Pediatric Disease Annotations & Medicines



   cerebellar degeneration
  

Disease ID 1720
Disease cerebellar degeneration
Definition
Degeneration of the cerebellum. It may be an inherited condition, a paraneoplastic syndrome, or secondary to autoimmune disorders.
Synonym
cerebellar degeneration (disorder)
cerebellar degeneration, nos
cerebellum--degeneration
degeneration of cerebellum
UMLS
C0262404
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:48)
C0004134  |  ataxia  |  11
C0007758  |  cerebellar ataxia  |  4
C1140680  |  ovarian ca  |  4
C1140680  |  ovarian cancer  |  4
C0001418  |  adenocarcinoma  |  3
C0028738  |  nystagmus  |  2
C0678222  |  breast carcinoma  |  2
C0006142  |  breast cancer  |  2
C0024299  |  lymphoma  |  2
C0149782  |  squamous cell carcinoma of the lung  |  1
C0031117  |  peripheral neuropathy  |  1
C0007112  |  adenocarcinoma of the prostate  |  1
C0752121  |  spinocerebellar ataxia type 2  |  1
C0019829  |  hodgkin lymphoma  |  1
C1527336  |  sjogren's syndrome  |  1
C0007137  |  squamous cell carcinoma  |  1
C0442874  |  neuropathy  |  1
C0334254  |  lymphoepithelial carcinoma  |  1
C0206718  |  ganglioneuroblastoma  |  1
C0007129  |  merkel cell carcinoma  |  1
C0024301  |  follicular lymphoma  |  1
C0242379  |  lung cancer  |  1
C0206701  |  serous carcinoma  |  1
C0001973  |  alcoholism  |  1
C0032290  |  aspiration pneumonia  |  1
C0679466  |  cognitive deficits  |  1
C0029132  |  optic neuropathy  |  1
C0005684  |  bladder cancer  |  1
C0005586  |  bipolar disorder  |  1
C0009207  |  cockayne syndrome  |  1
C0917796  |  leber's hereditary optic neuropathy  |  1
C0684249  |  carcinoma of the lung  |  1
C0524851  |  neurodegenerative disorders  |  1
C0677886  |  carcinoma of the ovary  |  1
C0149925  |  small cell lung cancer  |  1
C0007097  |  epithelial carcinoma  |  1
C0035304  |  retinal degeneration  |  1
C1335177  |  ovarian serous carcinoma  |  1
C0752120  |  spinocerebellar ataxia type 1  |  1
C0600139  |  carcinoma of the prostate  |  1
C0019829  |  hodgkin's lymphoma  |  1
C0345967  |  malignant mesothelioma  |  1
C0812413  |  pleural malignant mesothelioma  |  1
C0004138  |  hereditary ataxias  |  1
C0524851  |  neurodegenerative disease  |  1
C0039446  |  telangiectasia  |  1
C0004138  |  hereditary ataxia  |  1
C0032285  |  pneumonia  |  1
Curated Gene(Waiting for update.)
Inferring Gene(Waiting for update.)
Text Mined Gene(Waiting for update.)
Locus(Waiting for update.)
Disease ID 1720
Disease cerebellar degeneration
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:31)
HP:0001251  |  Ataxia  |  13
HP:0003002  |  Breast carcinoma  |  4
HP:0030731  |  Carcinoma  |  4
HP:0002073  |  Cerebellar ataxia, progressive  |  2
HP:0001310  |  Dysmetria  |  2
HP:0002665  |  Lymphoma  |  2
HP:0000639  |  Nystagmus  |  2
HP:0012189  |  Hodgkin disease  |  2
HP:0001009  |  Telangiectases  |  1
HP:0006747  |  Ganglioneuroblastoma  |  1
HP:0002860  |  Squamous cell carcinoma  |  1
HP:0002070  |  Appendicular ataxia  |  1
HP:0007302  |  Bipolar disorder  |  1
HP:0002090  |  Pneumonia  |  1
HP:0001337  |  Tremor  |  1
HP:0100001  |  Malignant mesothelioma  |  1
HP:0009725  |  Bladder neoplasm  |  1
HP:0002721  |  Immunodeficiency  |  1
HP:0100543  |  Cognitive deficits  |  1
HP:0000546  |  Retinal degeneration  |  1
HP:0002015  |  Swallowing difficulty  |  1
HP:0002960  |  Autoimmune condition  |  1
HP:0009830  |  Peripheral neuritis  |  1
HP:0001138  |  Damaged optic nerve  |  1
HP:0000708  |  Behavioral problems  |  1
HP:0011951  |  Aspiration pneumonia  |  1
HP:0001336  |  Myoclonic jerks  |  1
HP:0030357  |  Small cell lung carcinoma  |  1
HP:0010545  |  Downbeat nystagmus  |  1
HP:0100013  |  Tumours of the breast  |  1
HP:0002835  |  Aspiration  |  1
Disease ID 1720
Disease cerebellar degeneration
Manually Symptom
UMLS  | Name(Total Manually Symptoms:7)
C1135207  |  ataxia
C0740279  |  cerebellar atrophy
C0235169  |  excitability
C0233401  |  psychiatric symptoms
C0037116  |  silicosis
C0030472  |  paraneoplastic syndrome
C0020649  |  hypotension
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:1)
C0004134  |  ataxia  |  11
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:0)
(Waiting for update.)
GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)
GWASdb Snp Trait(Total Genotypes:0)
(Waiting for update.)
Mapped by lexical matching(Total Items:0)
(Waiting for update.)
Mapped by homologous gene(Total Items:0)
(Waiting for update.)
Chemical(Total Drugs:0)
(Waiting for update.)
FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)
FDA labeling changes(Total Drugs:0)
(Waiting for update.)