254112001: Osteoporosis with pseudoglioma (disorder)

SNOMED CT Concept\Clinical finding\...

\Functional finding\Abnormal bone formation\Osteogenesis imperfecta\Osteoporosis with pseudoglioma

\Musculoskeletal finding\Bone finding\Disorder of bone\Disorder of bone development\Congenital anomaly of skeletal bone\Osteogenesis imperfecta\Osteoporosis with pseudoglioma
\Musculoskeletal finding\Bone finding\Abnormal bone formation\Osteogenesis imperfecta\Osteoporosis with pseudoglioma
\Musculoskeletal finding\Disorder of musculoskeletal system\Disorder of skeletal system\Congenital skeletal dysplasia\Osteogenesis imperfecta\Osteoporosis with pseudoglioma
\Musculoskeletal finding\Disorder of musculoskeletal system\Disorder of skeletal system\Disorder of bone\Disorder of bone development\Congenital anomaly of skeletal bone\Osteogenesis imperfecta\Osteoporosis with pseudoglioma
\Musculoskeletal finding\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Osteogenesis imperfecta\Osteoporosis with pseudoglioma
\Musculoskeletal finding\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Osteogenesis imperfecta\Osteoporosis with pseudoglioma

\Disease\Genetic disease\Osteogenesis imperfecta\Osteoporosis with pseudoglioma
\Disease\Disorder of body system\Disorder of musculoskeletal system\Disorder of skeletal system\Congenital skeletal dysplasia\Osteogenesis imperfecta\Osteoporosis with pseudoglioma
\Disease\Disorder of body system\Disorder of musculoskeletal system\Disorder of skeletal system\Disorder of bone\Disorder of bone development\Congenital anomaly of skeletal bone\Osteogenesis imperfecta\Osteoporosis with pseudoglioma
\Disease\Disorder of body system\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Osteogenesis imperfecta\Osteoporosis with pseudoglioma
\Disease\Disorder of body system\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Osteogenesis imperfecta\Osteoporosis with pseudoglioma
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Osteogenesis imperfecta\Osteoporosis with pseudoglioma
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Osteogenesis imperfecta\Osteoporosis with pseudoglioma
\Disease\Developmental disorder\Disorder of bone development\Congenital anomaly of skeletal bone\Osteogenesis imperfecta\Osteoporosis with pseudoglioma
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Osteogenesis imperfecta\Osteoporosis with pseudoglioma
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Osteogenesis imperfecta\Osteoporosis with pseudoglioma

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

378273015 Osteoporosis with pseudoglioma en Synonym Active Entire term case insensitive SNOMED CT core module

644958015 Osteoporosis with pseudoglioma (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Osteoporosis with pseudoglioma	Is a	Osteogenesis imperfecta	true	Inferred relationship	Existential restriction modifier
Osteoporosis with pseudoglioma	Associated morphology	Dysplasia	true	Inferred relationship	Existential restriction modifier	1
Osteoporosis with pseudoglioma	Finding site	Skeletal system structure	false	Inferred relationship	Existential restriction modifier	1
Osteoporosis with pseudoglioma	Finding site	Connective tissue structure	false	Inferred relationship	Existential restriction modifier
Osteoporosis with pseudoglioma	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier
Osteoporosis with pseudoglioma	Finding site	Connective tissue	false	Inferred relationship	Existential restriction modifier
Osteoporosis with pseudoglioma	Finding site	Bone structure	true	Inferred relationship	Existential restriction modifier	1
Osteoporosis with pseudoglioma	Associated morphology	Congenital dysplasia	false	Inferred relationship	Existential restriction modifier	1
Osteoporosis with pseudoglioma	Associated morphology	Congenital dysplasia	false	Inferred relationship	Existential restriction modifier	1
Osteoporosis with pseudoglioma	Finding site	Bone structure	false	Inferred relationship	Existential restriction modifier	1
Osteoporosis with pseudoglioma	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier	2
Osteoporosis with pseudoglioma	Finding site	Bone structure	false	Inferred relationship	Existential restriction modifier	2
Osteoporosis with pseudoglioma	Associated morphology	Congenital dysplasia	false	Inferred relationship	Existential restriction modifier	2
Osteoporosis with pseudoglioma	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	1
Osteoporosis with pseudoglioma	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Osteoporosis with pseudoglioma	Has interpretation	Abnormal	true	Inferred relationship	Existential restriction modifier	2
Osteoporosis with pseudoglioma	Interprets	Bone formation, function	true	Inferred relationship	Existential restriction modifier	2

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
378273015	Osteoporosis with pseudoglioma	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
644958015	Osteoporosis with pseudoglioma (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module