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13331008: Atrophy (morphologic abnormality)

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

Descriptions:

Id Description Lang Type Status Case? Module
22797016 Atrophy en Synonym Active Entire term case insensitive SNOMED CT core module
737978016 Atrophy (morphologic abnormality) en Fully specified name Active Entire term case insensitive SNOMED CT core module
1220945019 Atrophic en Synonym Active Entire term case insensitive SNOMED CT core module

41 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Atrophy Is a Degenerative abnormality false Inferred relationship Existential restriction modifier
Atrophy Is a Degeneration false Inferred relationship Existential restriction modifier
Atrophy Is a Degenerative abnormality true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
Placenta fenestrata Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Mitochondrial myopathy, cerebellar ataxia, pigmentary retinopathy syndrome Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Short stature, optic nerve atrophy, Pelger-Huët anomaly syndrome Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Autosomal recessive cerebellar ataxia due to CWF19 like cell cycle control factor 1 deficiency Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
NAD(P)HX dehydratase deficiency Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Atrophic cervicitis Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Muscle wasting NEC Associated morphology False Atrophy Inferred relationship Existential restriction modifier 1
Muscle wasting NEC Associated morphology False Atrophy Inferred relationship Existential restriction modifier 1
[X]Dementia in Pick's disease Associated morphology False Atrophy Inferred relationship Existential restriction modifier 1
[X]Other atrophic disorders of skin Associated morphology False Atrophy Inferred relationship Existential restriction modifier 1
Unspecified optic atrophy Associated morphology False Atrophy Inferred relationship Existential restriction modifier 1
Optic atrophy NOS Associated morphology False Atrophy Inferred relationship Existential restriction modifier 1
Muscle wasting and disuse atrophy NEC Associated morphology False Atrophy Inferred relationship Existential restriction modifier 1
Amyotrophia NOS Associated morphology False Atrophy Inferred relationship Existential restriction modifier 1
Atrophy of salivary gland NOS Associated morphology False Atrophy Inferred relationship Existential restriction modifier 1
Tongue papillary atrophy NOS Associated morphology False Atrophy Inferred relationship Existential restriction modifier 1
Muscle wasting/disuse atrophy NEC NOS Associated morphology False Atrophy Inferred relationship Existential restriction modifier 1
Striae atrophicae NOS Associated morphology False Atrophy Inferred relationship Existential restriction modifier 1
Muscle wasting/atrophy NOS Associated morphology False Atrophy Inferred relationship Existential restriction modifier 1
Algoneurodystrophy NOS Associated morphology False Atrophy Inferred relationship Existential restriction modifier
Facial lipoatrophy associated with human immunodeficiency virus Associated morphology True Atrophy Inferred relationship Existential restriction modifier 2

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