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EXPERIMENTAL FACTOR ONTOLOGY - ANNOTATIONS

Term:Parkinson disease
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Accession:EFO:MONDO:0005180 term browser browse the term
Definition:A progressive degenerative disorder of the central nervous system characterized by loss of dopamine producing neurons in the substantia nigra and the presence of Lewy bodies in the substantia nigra and locus coeruleus. Signs and symptoms include tremor which is most pronounced during rest, muscle rigidity, slowing of the voluntary movements, a tendency to fall back, and a mask-like facial expression.
Synonyms:exact_synonym: PD;   Parkinson's disease;   paralysis agitans
 alt_id: MONDO:0005180
 xref: DOID:14330;   ICD9:332;   ICD9:332.0;   MEDGEN:10590;   MESH:D010300;   MIM:PS168600;   NANDO:1200010;   NCI:C26845;   NIFSTD:birnlex_2098;   ORDO:319705;   SCTID:49049000;   UMLS:C0030567;   icd11.foundation:296066191


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Path 1
Term Annotations click to browse term
  experimental factor 0
    material property 0
      disposition 0
        disease 0
          genetic disorder 0
            hereditary neurological disease 0
              Parkinson disease 0
                Hereditary late-onset Parkinson disease 0
                Parkinson disease, dominant 0
                Parkinson disease, mitochondrial 0
                Young adult-onset Parkinsonism 0
                late-onset Parkinson disease + 0
                parkinson disease 25, autosomal recessive early-onset, with impaired intellectual development 0
                parkinsonian-pyramidal syndrome 0
                secondary Parkinson disease + 0
                young-onset Parkinson disease + 0
Path 2
Term Annotations click to browse term
  experimental factor 0
    material property 0
      disposition 0
        disease 0
          nervous system disease 0
            central nervous system disease 0
              brain disease 0
                basal ganglia disease 0
                  parkinsonian disorder 0
                    Parkinson disease 0
                      Hereditary late-onset Parkinson disease 0
                      Parkinson disease, dominant 0
                      Parkinson disease, mitochondrial 0
                      Young adult-onset Parkinsonism 0
                      late-onset Parkinson disease + 0
                      parkinson disease 25, autosomal recessive early-onset, with impaired intellectual development 0
                      parkinsonian-pyramidal syndrome 0
                      secondary Parkinson disease + 0
                      young-onset Parkinson disease + 0
paths to the root