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128420001: Demineralized structure (morphologic abnormality)


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
206722012 Demineralization en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
206723019 Demineralized structure en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
474397016 Demineralised structure en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
474398014 Demineralisation en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
732411015 Demineralized structure (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
206722012 Demineralization en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
206722012 Demineralization en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
206723019 Demineralized structure en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
206723019 Demineralized structure en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
474397016 Demineralised structure en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
474397016 Demineralised structure en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
474398014 Demineralisation en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
474398014 Demineralisation en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
732411015 Demineralized structure (morphologic abnormality) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
732411015 Demineralized structure (morphologic abnormality) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
732411015 Demineralized structure (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Demineralized structure Is a Depletion (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group
Eiken syndrome Associated morphology True Demineralized structure Inferred relationship Existential restriction modifier (core metadata concept) 2
A rare syndrome characterized by sparse hair, osteopenia, intellectual disability, minor facial abnormalities, joint laxity and hypotonia. There have been no further descriptions in the literature since 1992. Associated morphology True Demineralized structure Inferred relationship Existential restriction modifier (core metadata concept) 2
Osteopenia with high fracture risk (disorder) Associated morphology True Demineralized structure Inferred relationship Existential restriction modifier (core metadata concept) 1
Osteopenia following menopause (disorder) Associated morphology True Demineralized structure Inferred relationship Existential restriction modifier (core metadata concept) 1
Osteopenia due to disuse (disorder) Associated morphology True Demineralized structure Inferred relationship Existential restriction modifier (core metadata concept) 1
Osteopenia caused by drug (disorder) Associated morphology True Demineralized structure Inferred relationship Existential restriction modifier (core metadata concept) 1
Neurodevelopmental delay, seizures, ophthalmic anomalies, osteopenia, cerebellar atrophy syndrome Associated morphology True Demineralized structure Inferred relationship Existential restriction modifier (core metadata concept) 3
Premenopausal idiopathic osteopenia (disorder) Associated morphology True Demineralized structure Inferred relationship Existential restriction modifier (core metadata concept) 1
A rare syndromic intellectual disability characterised by intellectual deficit, short stature, obesity, genital abnormalities, and hand and/or toe contractures. The patients also present with generalised osteoporosis and a history of frequent fractures. This syndrome is similar to Prader-Willi syndrome, but the hand contractures and osteoporosis, together with the lack of hypotonia, indicate this is a different entity. Associated morphology True Demineralized structure Inferred relationship Existential restriction modifier (core metadata concept) 5
Secondary osteoporotic fracture of lumbar vertebra Associated morphology True Demineralized structure Inferred relationship Existential restriction modifier (core metadata concept) 1
Osteoporosis caused by ionizing radiation Associated morphology True Demineralized structure Inferred relationship Existential restriction modifier (core metadata concept) 1
Osteoporosis due to and following radiotherapy Associated morphology True Demineralized structure Inferred relationship Existential restriction modifier (core metadata concept) 1

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