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:

Expanded Value Set

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

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Senile osteopenia	Associated morphology	False	Osteopenia	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Steroid-induced osteopenia (disorder)	Associated morphology	False	Osteopenia	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Osteopenia	Associated morphology	False	Osteopenia	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Osteopenia	Associated morphology	False	Osteopenia	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Senile osteopenia	Associated morphology	False	Osteopenia	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Steroid-induced osteopenia (disorder)	Associated morphology	False	Osteopenia	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Osteopenia of prematurity	Associated morphology	False	Osteopenia	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Osteopenia of prematurity	Associated morphology	False	Osteopenia	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Neonatal osteopenia (disorder)	Associated morphology	False	Osteopenia	Inferred relationship	Existential restriction modifier (core metadata concept)	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	Osteopenia	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Eiken syndrome	Associated morphology	False	Osteopenia	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Osteopenia with high fracture risk (disorder)	Associated morphology	False	Osteopenia	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Ichthyose-Hypotrichose-Syndrom	Associated morphology	False	Osteopenia	Inferred relationship	Existential restriction modifier (core metadata concept)	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	Osteopenia	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Osteopenia caused by drug (disorder)	Associated morphology	False	Osteopenia	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Premenopausal idiopathic osteopenia (disorder)	Associated morphology	False	Osteopenia	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Osteopenia following menopause (disorder)	Associated morphology	False	Osteopenia	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Osteopenia due to disuse (disorder)	Associated morphology	False	Osteopenia	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Eiken syndrome	Associated morphology	False	Osteopenia	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Ichthyose-Hypotrichose-Syndrom	Associated morphology	False	Osteopenia	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	False	Osteopenia	Inferred relationship	Existential restriction modifier (core metadata concept)	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	Osteopenia	Inferred relationship	Existential restriction modifier (core metadata concept)	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	Osteopenia	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Neonatal osteopenia (disorder)	Associated morphology	False	Osteopenia	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Neurodevelopmental delay, seizures, ophthalmic anomalies, osteopenia, cerebellar atrophy syndrome	Associated morphology	False	Osteopenia	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Osteopenia following menopause (disorder)	Associated morphology	False	Osteopenia	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Reference Sets

Concept inactivation indicator attribute value reference set (foundation metadata concept)

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
130166010	Osteopenia	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
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	Only initial character 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