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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


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Demineralized structure Is a Depletion true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
A rare, genetic, primary bone dysplasia syndrome characterized by multiple epiphyseal dysplasia, severely delayed ossification (mainly of the epiphyses, pubic symphysis, hands and feet), abnormal modeling of the bones in hands and feet, abnormal pelvis cartilage persistence, and mild growth retardation. Calcium, phosphate and vitamin D serum levels are typically within normal range, while parathyroid hormone serum levels are normal to slightly elevated. Oligodontia has been rarely associated. Associated morphology True Demineralized structure Inferred relationship Some 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 Some 2
Osteopenia with high fracture risk (disorder) Associated morphology True Demineralized structure Inferred relationship Some 1
Osteopenia following menopause (disorder) Associated morphology True Demineralized structure Inferred relationship Some 1
Osteopenia due to disuse (disorder) Associated morphology True Demineralized structure Inferred relationship Some 1
Osteopenia caused by drug (disorder) Associated morphology True Demineralized structure Inferred relationship Some 1
A rare, genetic, syndromic intellectual disability characterized by global developmental delay, early-onset seizures, cerebellar atrophy, osteopenia, nystagmus and dysmorphic facial features, including bitemporal narrowing, prominent forehead, anteverted nares. Dysarthria, dysmetria, ataxic gait, spasticity and dysmorphic features have also been associated. Associated morphology True Demineralized structure Inferred relationship Some 3
Premenopausal idiopathic osteopenia (disorder) Associated morphology True Demineralized structure Inferred relationship Some 1
A rare syndromic intellectual disability characterized by intellectual deficit, short stature, obesity, genital abnormalities, and hand and/or toe contractures. The patients also present with generalized 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 Some 5
Secondary osteoporotic fracture of lumbar vertebra Associated morphology True Demineralized structure Inferred relationship Some 1
Osteoporosis caused by ionizing radiation Associated morphology True Demineralized structure Inferred relationship Some 1
Osteoporosis due to and following radiotherapy Associated morphology True Demineralized structure Inferred relationship Some 1

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