DiseaseID 4854

青少年型帕金森病

disease

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Disease: 1Symptom: 9Target: 12Links: 21

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Record Fields

Scalar fields from the final disease record.

Disease Id: 4854
Core Entity Id: 61267
Source Entity Count: 1
Preferred Name: Parkinsonism, Juvenile
Name Cn: 青少年型帕金森病
Name Pinyin: Qing Shao Nian Xing Pa Jin Sen Bing
Name En: Parkinsonism, Juvenile
Name Latin
Bilingual Status: complete
Disease Type: disease
Umls Disease Type: Disease or Syndrome
Disgenet Type: disease
Mesh Class: Nervous System Diseases
Do Class: disease of anatomical entitydisease of anatomical entity; genetic disease
Hpo Class: Abnormality of the nervous system
Mesh Class Name: Nervous System Diseases
Hpo Class Name: Abnormality of the nervous system
Do Class Name: disease of anatomical entitygenetic disease; disease of anatomical entity
Disease Definition: MSH2017_2016_08_12:Conditions which feature clinical manifestations resembling primary Parkinson disease that are caused by a known or suspected condition. Examples include parkinsonism caused by vascular injury, drugs, trauma, toxin exposure, neoplasms, infections and degenerative or hereditary conditions. Clinical features may include bradykinesia, rigidity, parkinsonian gait, and masked facies. In general, tremor is less prominent in secondary parkinsonism than in the primary form. (From Joynt, Clinical Neurology, 1998, Ch38, pp39-42)
Version: v1
Suppressed: No

Names

Preferred names, aliases, and source labels retained in the final schema.

Name

Parkinsonism, Juvenile

Role

preferred

Name

Parkinson Disease 2, Autosomal Recessive Juvenile

Role

preferred

Name

Parkinsonian Disorders

Role

preferred

Name

Secondary Parkinson Disease

Role

preferred

Name

Atherosclerotic Parkinsonism

Role

preferred

Name

Autosomal Dominant Juvenile Parkinson Disease

Role

preferred

Name

Autosomal Dominant Parkinsonism

Role

preferred

Name

Autosomal Recessive Parkinsonism

Role

preferred

Name

Familial Juvenile Parkinsonism

Role

preferred

Name

Parkinson Disease, Secondary Vascular

Role

preferred

Name

Parkinsonism, Experimental

Role

preferred

Name

Ramsay Hunt Paralysis Syndrome

Role

preferred

Name

EPDF

Role

alias

Name

PARK2

Role

alias

Name

PARKINSON DISEASE, JUVENILE, AUTOSOMAL RECESSIVE

Role

alias

Name

PARKINSONISM, EARLY-ONSET, WITH DIURNAL FLUCTUATION

Role

alias

Name

PDJ

Role

alias

Name

Parkinson Disease, Secondary

Role

alias

Name

Parkinson'S Disease 2

Role

alias

Name

Parkinsonian Disease

Role

alias

Name

Parkinsonism

Role

alias

Name

Secondary Parkinsonism

Role

alias

Name

Secondary Parkinsonism, Unspecified

Role

alias

Cross References

Trusted external identifiers retained for this final record.

Hpo

HP:0001300

Herb

HBDIS002315HBDIS005423HBDIS005424HBDIS011286HBDIS011287HBDIS011535HBDIS011536HBDIS011537HBDIS011538HBDIS011539HBDIS011540HBDIS018467

Me Sh

D010302D020734

Omim

600116

Umls

C0030569C0242422C1868675

Icd10

G21G21.9

Sym Map

SMDE04121SMDE11961SMDE13022

Do Class

DOID:630DOID:7

Dis Ge Net

C0030569C0242422C0242423C0751414C0751415C0752097C0752098C0752100C0752101C0752104C0752105C1868675

Umls Sty

T047T050

Hpo Class

HP:0000707

Me Sh Class

C10

Tcmbank Disease

10775117201458615019183422273125493263212699928161569396109781

Itcmdb Generated

ITX-DISEASE-0A1B349D2254ITX-DISEASE-1D6DEAC9AC65

Attributes

Merged source attributes and domain-specific metadata.

Version

v1v2

Suppress

Do Class Name

disease of anatomical entitygenetic disease; disease of anatomical entity

Disease Type

diseasegroup

Hpo Class Name

Abnormality of the nervous system

Do Disease Class

disease of anatomical entitydisease of anatomical entity; genetic disease

Hpo Disease Class

Abnormality of the nervous system

Umls Disease Type

Disease or SyndromeExperimental Model of Disease

Disease Definition

MSH2017_2016_08_12:Conditions which feature clinical manifestations resembling primary Parkinson disease that are caused by a known or suspected condition. Examples include parkinsonism caused by vascular injury, drugs, trauma, toxin exposure, neoplasms, infections and degenerative or hereditary conditions. Clinical features may include bradykinesia, rigidity, parkinsonian gait, and masked facies. In general, tremor is less prominent in secondary parkinsonism than in the primary form. (From Joynt, Clinical Neurology, 1998, Ch38, pp39-42)PSY2004:Clinical state, usually drug induced, characterized by tremors, muscle rigidity, postural reflex dysfunction, and akinesia. Compare PARKINSONS DISEASE.|NCI2016_NICHD_1602D:One or more of the following symptoms including bradykinesia associated with rigidity, resting tremor, gait disturbance, which may be due to multiple etiologies.|NCI2016_02D:One or more of the following symptoms including bradykinesia associated with rigidity, resting tremor, gait disturbance, which may be due to multiple etiologies.|MSH2017_2016_08_12:A group of disorders which feature impaired motor control characterized by bradykinesia, MUSCLE RIGIDITY; TREMOR; and postural instability. Parkinsonian diseases are generally divided into primary parkinsonism (see PARKINSON DISEASE), secondary parkinsonism (see PARKINSON DISEASE, SECONDARY) and inherited forms. These conditions are associated with dysfunction of dopaminergic or closely related motor integration neuronal pathways in the BASAL GANGLIA.|HPO2016_07_04:Characteristic neurologic anomaly resulting form degeneration of dopamine-generating cells in the substantia nigra, a region of the midbrain, characterized clinically by shaking, rigidity, slowness of movement and difficulty with walking and gait. [HPO:probinson]

Me Sh Disease Class

Nervous System Diseases

Dis Ge Net Disease Type

diseasegroup

Disease Class Name Me Sh

Nervous System Diseases

Umls Semantic Type Name

Disease or SyndromeExperimental Model of Disease