FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

312894000: Osteopenia (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Dec 2023. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
456694019 Osteopenia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
709616015 Osteopenia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3990916015 Bone loss en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5282564018 A decrease in bone mineral density with a T-score via DEXA (dual-energy X-ray absorptiometry) bone scan between -1 and -2.5. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
456694019 Osteopenia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
456694019 Osteopenia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
709616015 Osteopenia (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
709616015 Osteopenia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3990916015 Bone loss en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5282564018 A decrease in bone mineral density with a T-score via DEXA (dual-energy X-ray absorptiometry) bone scan between -1 and -2.5. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
857071000195119 Osteopenie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
85421000077111 ostéopénie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
85421000077111 ostéopénie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
857071000195119 Osteopenie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

15 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Osteopenia Is a Disorder of bone and articular cartilage false Inferred relationship Existential restriction modifier (core metadata concept)
Osteopenia Finding site Skeletal system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Osteopenia Finding site Cartilaginous tissue structure false Inferred relationship Existential restriction modifier (core metadata concept)
Osteopenia Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Osteopenia Is a Disorder of bone (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Osteopenia Associated morphology Osteopenia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Osteopenia Is a Degenerative disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Osteopenia Associated morphology Osteopenia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Osteopenia Finding site Bone structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Osteopenia Is a Degenerative disorder of bone true Inferred relationship Existential restriction modifier (core metadata concept)
Osteopenia Associated morphology Demineralized structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Senile osteopenia Is a True Osteopenia Inferred relationship Existential restriction modifier (core metadata concept)
Steroid-induced osteopenia (disorder) Is a True Osteopenia Inferred relationship Existential restriction modifier (core metadata concept)
Family history of osteopenia (situation) Associated finding False Osteopenia Inferred relationship Existential restriction modifier (core metadata concept) 1
Family history of osteopenia (situation) Associated finding True Osteopenia Inferred relationship Existential restriction modifier (core metadata concept) 1
Osteopenia of prematurity Is a False Osteopenia Inferred relationship Existential restriction modifier (core metadata concept)
Family history of osteopenia (situation) Associated finding False Osteopenia Inferred relationship Existential restriction modifier (core metadata concept) 1
History of osteopenia resolved (situation) Associated finding True Osteopenia Inferred relationship Existential restriction modifier (core metadata concept) 1
History of osteopenia Associated finding True Osteopenia Inferred relationship Existential restriction modifier (core metadata concept) 1
Neonatal osteopenia (disorder) Is a True Osteopenia Inferred relationship Existential restriction modifier (core metadata concept)
Eiken syndrome Is a True Osteopenia Inferred relationship Existential restriction modifier (core metadata concept)
A rare genetic disease characterized by global developmental delay with language and cognition deficiencies, behavioral problems, osteopenia, joint laxity, skin defects consisting of hyperkeratosis and sweat gland and melanocyte abnormalities with hypopigmented areas, and abnormal hair structure. Mild facial dysmorphism (prominent forehead, thick eyebrows, epicanthal folds, broad nasal bridge, long philtrum, and micrognathia), abnormalities of the teeth, and skeletal and cardiac anomalies have also been described. Is a True Osteopenia Inferred relationship Existential restriction modifier (core metadata concept)
Osteopenia with high fracture risk (disorder) Is a True Osteopenia Inferred relationship Existential restriction modifier (core metadata concept)
Ichthyose-Hypotrichose-Syndrom Is a False Osteopenia Inferred relationship Existential restriction modifier (core metadata concept)
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. Is a True Osteopenia Inferred relationship Existential restriction modifier (core metadata concept)
Osteopenia caused by drug (disorder) Is a True Osteopenia Inferred relationship Existential restriction modifier (core metadata concept)
Premenopausal idiopathic osteopenia (disorder) Is a True Osteopenia Inferred relationship Existential restriction modifier (core metadata concept)
Osteopenia following menopause (disorder) Is a True Osteopenia Inferred relationship Existential restriction modifier (core metadata concept)
Osteopenia due to disuse (disorder) Is a True Osteopenia Inferred relationship Existential restriction modifier (core metadata concept)
A rare genetic developmental defect during embryogenesis disorder with characteristics of craniofacial dysmorphism (including brachycephaly, prominent forehead, sparse lateral eyebrows, severe hypertelorism, upslanting palpebral fissures, epicanthal folds, protruding ears, broad nasal bridge, pointed nasal tip, flat philtrum, anteverted nostrils, large mouth, thin upper vermilion border, highly arched palate and mild micrognathia) associated with osteopenia leading to repeated long bone fractures, severe myopia, mild to moderate sensorineural or mixed hearing loss, enamel hypoplasia, sloping shoulders and mild intellectual disability. There is evidence the disease can be caused by homozygous mutation in the IRX5 gene on chromosome 16q11.2. Is a True Osteopenia Inferred relationship Existential restriction modifier (core metadata concept)
Neurodevelopmental delay, seizures, ophthalmic anomalies, osteopenia, cerebellar atrophy syndrome Is a True Osteopenia Inferred relationship Existential restriction modifier (core metadata concept)
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. Is a True Osteopenia Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

Back to Start