737582007: syndroom van hemiparkinsonisme en hemiatrofie (aandoening)

Descriptions:

Id Description Lang Type Status Case? Module

3528395016 Hemiparkinsonism hemiatrophy syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

3528396015 Hemiparkinsonism hemiatrophy syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

9388831000146112 syndroom van hemiparkinsonisme en hemiatrofie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

9388841000146116 syndroom van hemiparkinsonisme en hemiatrofie (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

3528397012 A rare parkinsonian disorder with characteristics of unilateral body atrophy and slowly progressive, ipsilateral hemiparkinsonian signs (bradykinesia, rigidity, and tremor). Patients typically present with unilateral, action-induced dystonia, in upper or lower limbs, that progresses and becomes bilateral or with tremor which occurs predominantly at rest and progresses to hemiparkinsonism. Scoliosis, scapular winging, raised shoulders, brisk reflexes and extensor plantars are frequently associated. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hemiparkinsonism hemiatrophy syndrome (disorder)	Is a	Parkinsonism	true	Inferred relationship	Some
Hemiparkinsonism hemiatrophy syndrome (disorder)	Is a	Degenerative disorder	true	Inferred relationship	Some
Hemiparkinsonism hemiatrophy syndrome (disorder)	Finding site	Basal ganglion structure (body structure)	true	Inferred relationship	Some	1
Hemiparkinsonism hemiatrophy syndrome (disorder)	Associated morphology	Hemiatrophy	true	Inferred relationship	Some	2
Hemiparkinsonism hemiatrophy syndrome (disorder)	Finding site	Structure of half of body lateral to midsagittal plane (body structure)	true	Inferred relationship	Some	2
Hemiparkinsonism hemiatrophy syndrome (disorder)	Interprets	Movement	true	Inferred relationship	Some	4
Hemiparkinsonism hemiatrophy syndrome (disorder)	Has interpretation	Slow	true	Inferred relationship	Some	4

Inbound Relationships

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This concept is not in any reference sets

Id	Description	Lang	Type	Status	Case?	Module
3528395016	Hemiparkinsonism hemiatrophy syndrome (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3528396015	Hemiparkinsonism hemiatrophy syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
9388831000146112	syndroom van hemiparkinsonisme en hemiatrofie	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
9388841000146116	syndroom van hemiparkinsonisme en hemiatrofie (aandoening)	nl	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
3528397012	A rare parkinsonian disorder with characteristics of unilateral body atrophy and slowly progressive, ipsilateral hemiparkinsonian signs (bradykinesia, rigidity, and tremor). Patients typically present with unilateral, action-induced dystonia, in upper or lower limbs, that progresses and becomes bilateral or with tremor which occurs predominantly at rest and progresses to hemiparkinsonism. Scoliosis, scapular winging, raised shoulders, brisk reflexes and extensor plantars are frequently associated.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core