34087007: Hemiatrophy (morphologic abnormality)

SNOMED CT Concept\Body structure (body structure)\Morphologically altered structure\Morphologically abnormal structure\Degenerative abnormality\Atrophy\Hemiatrophy

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

56929018 Hemiatrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

765568016 Hemiatrophy (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hemiatrophy	Is a	Atrophy	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Facial hemiatrophy	Associated morphology	False	Hemiatrophy	Inferred relationship	Some	1
Facial hemiatrophy	Associated morphology	False	Hemiatrophy	Inferred relationship	Some	1
Facial hemiatrophy	Associated morphology	True	Hemiatrophy	Inferred relationship	Some	3
Hemiatrophy of lower limb	Associated morphology	True	Hemiatrophy	Inferred relationship	Some	1
Progressive hemifacial atrophy (PHA) is a rare acquired disorder, characterized by unilateral slowly progressive atrophy of the skin and soft tissues of half of the face leading to a sunken appearance. Muscles, cartilage and the underlying bony structures may also be involved.	Associated morphology	True	Hemiatrophy	Inferred relationship	Some	1
Hemidystonia-hemiatrophy (HD-HA) is a rare dystonia, usually caused by a static cerebral injury occurring at birth or during infancy, that is characterized by a combination of hemidystonia (HD), involving one half of the body, and hemiatrophy (HA) on the same side as the HD.	Associated morphology	True	Hemiatrophy	Inferred relationship	Some	2
Hemiparkinsonism-hemiatrophy syndrome is a rare parkinsonian disorder characterized by 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 plantar responses are frequently associated.	Associated morphology	True	Hemiatrophy	Inferred relationship	Some	2
Hemiatrophy of tongue (disorder)	Associated morphology	True	Hemiatrophy	Inferred relationship	Some	1
Hemiatrophy of upper limb	Associated morphology	True	Hemiatrophy	Inferred relationship	Some	1
Hemiatrophy of cerebellar cortex	Associated morphology	True	Hemiatrophy	Inferred relationship	Some	1
Hemiatrophy of cerebral cortex	Associated morphology	True	Hemiatrophy	Inferred relationship	Some	1

This concept is not in any reference sets