78441005: Osteopenia (morphologic abnormality)

Status: retired, 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

130166010 Osteopenia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

819382011 Osteopenia (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

2512121000005117 osteopeni da Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Danish module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
osteopeni	Is a	Depletion	false	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Senile osteopenia	Associated morphology	False	osteopeni	Inferred relationship	Some	1
Steroid-induced osteopenia (disorder)	Associated morphology	False	osteopeni	Inferred relationship	Some	1
A decrease in bone mineral density with a T-score via DEXA (dual-energy X-ray absorptiometry) bone scan between -1 and -2.5.	Associated morphology	False	osteopeni	Inferred relationship	Some	1
A decrease in bone mineral density with a T-score via DEXA (dual-energy X-ray absorptiometry) bone scan between -1 and -2.5.	Associated morphology	False	osteopeni	Inferred relationship	Some	1
Senile osteopenia	Associated morphology	False	osteopeni	Inferred relationship	Some	1
Steroid-induced osteopenia (disorder)	Associated morphology	False	osteopeni	Inferred relationship	Some	1
Osteopenia of prematurity	Associated morphology	False	osteopeni	Inferred relationship	Some	1
Osteopenia of prematurity	Associated morphology	False	osteopeni	Inferred relationship	Some	1
Neonatal osteopenia (disorder)	Associated morphology	False	osteopeni	Inferred relationship	Some	2
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.	Associated morphology	False	osteopeni	Inferred relationship	Some	2
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	False	osteopeni	Inferred relationship	Some	3
Osteopenia with high fracture risk (disorder)	Associated morphology	False	osteopeni	Inferred relationship	Some	1
Osteopenia, myopia, hearing loss, intellectual disability, facial dysmorphism syndrome	Associated morphology	False	osteopeni	Inferred relationship	Some	5
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	False	osteopeni	Inferred relationship	Some	4
Osteopenia caused by drug (disorder)	Associated morphology	False	osteopeni	Inferred relationship	Some	1
Premenopausal idiopathic osteopenia (disorder)	Associated morphology	False	osteopeni	Inferred relationship	Some	1
Osteopenia following menopause (disorder)	Associated morphology	False	osteopeni	Inferred relationship	Some	2
Osteopenia due to disuse (disorder)	Associated morphology	False	osteopeni	Inferred relationship	Some	1
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	False	osteopeni	Inferred relationship	Some	2
Osteopenia, myopia, hearing loss, intellectual disability, facial dysmorphism syndrome	Associated morphology	False	osteopeni	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	False	osteopeni	Inferred relationship	Some	2
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.	Associated morphology	False	osteopeni	Inferred relationship	Some	1
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.	Associated morphology	False	osteopeni	Inferred relationship	Some	3
Neonatal osteopenia (disorder)	Associated morphology	False	osteopeni	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	False	osteopeni	Inferred relationship	Some	3
Osteopenia following menopause (disorder)	Associated morphology	False	osteopeni	Inferred relationship	Some	1

Reference Sets

Concept inactivation indicator reference set

REPLACED BY association reference set (foundation metadata concept)

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Id	Description	Lang	Type	Status	Case?	Module
130166010	Osteopenia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
819382011	Osteopenia (morphologic abnormality)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2512121000005117	osteopeni	da	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Danish module (core metadata concept)