254121000: Osteopetrosis - intermediate type (disorder)

SNOMED CT Concept\Clinical finding\...

\Musculoskeletal finding\Bone finding\Disorder of bone\Disorder of bone development\Congenital anomaly of skeletal bone\Osteopetrosis\Osteopetrosis - intermediate type
\Musculoskeletal finding\Disorder of musculoskeletal system\Hereditary disorder of musculoskeletal system\Osteopetrosis\Osteopetrosis - intermediate type
\Musculoskeletal finding\Disorder of musculoskeletal system\Chronic disease of musculoskeletal system\Osteopetrosis\Osteopetrosis - intermediate type
\Musculoskeletal finding\Disorder of musculoskeletal system\Disorder of skeletal system\Disorder of bone\Disorder of bone development\Congenital anomaly of skeletal bone\Osteopetrosis\Osteopetrosis - intermediate type
\Musculoskeletal finding\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Osteopetrosis\Osteopetrosis - intermediate type

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Osteopetrosis\Osteopetrosis - intermediate type
\Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Osteopetrosis\Osteopetrosis - intermediate type
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Osteopetrosis\Osteopetrosis - intermediate type
\Disease\Disorder of body system\Disorder of musculoskeletal system\Hereditary disorder of musculoskeletal system\Osteopetrosis\Osteopetrosis - intermediate type
\Disease\Disorder of body system\Disorder of musculoskeletal system\Chronic disease of musculoskeletal system\Osteopetrosis\Osteopetrosis - intermediate type
\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\Osteopetrosis\Osteopetrosis - intermediate type
\Disease\Disorder of body system\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Osteopetrosis\Osteopetrosis - intermediate type
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Osteopetrosis\Osteopetrosis - intermediate type
\Disease\Chronic disease\Chronic disease of musculoskeletal system\Osteopetrosis\Osteopetrosis - intermediate type
\Disease\Developmental disorder\Disorder of bone development\Congenital anomaly of skeletal bone\Osteopetrosis\Osteopetrosis - intermediate type
\Disease\Developmental disorder\Developmental hereditary disorder\Osteopetrosis\Osteopetrosis - intermediate type
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Osteopetrosis\Osteopetrosis - intermediate type

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

378286012 Osteopetrosis - intermediate type en Synonym Active Entire term case insensitive SNOMED CT core module

644969017 Osteopetrosis - intermediate type (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
Osteopetrosis - intermediate type	Is a	Osteopetrosis	true	Inferred relationship	Existential restriction modifier
Osteopetrosis - intermediate type	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier
Osteopetrosis - intermediate type	Finding site	Bone structure	true	Inferred relationship	Existential restriction modifier	1
Osteopetrosis - intermediate type	Associated morphology	Congenital anomaly	false	Inferred relationship	Existential restriction modifier	1
Osteopetrosis - intermediate type	Finding site	Bone structure	false	Inferred relationship	Existential restriction modifier	1
Osteopetrosis - intermediate type	Associated morphology	Congenital anomaly	false	Inferred relationship	Existential restriction modifier	1
Osteopetrosis - intermediate type	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier	2
Osteopetrosis - intermediate type	Associated morphology	Developmental anomaly	false	Inferred relationship	Existential restriction modifier	2
Osteopetrosis - intermediate type	Finding site	Bone structure	false	Inferred relationship	Existential restriction modifier	2
Osteopetrosis - intermediate type	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Osteopetrosis - intermediate type	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	1
Osteopetrosis - intermediate type	Associated morphology	Morphologically abnormal structure	true	Inferred relationship	Existential restriction modifier	1
Osteopetrosis - intermediate type	Has interpretation	Below reference range	true	Inferred relationship	Existential restriction modifier	2
Osteopetrosis - intermediate type	Interprets	Osteoclast turnover rate	true	Inferred relationship	Existential restriction modifier	2
Osteopetrosis - intermediate type	Clinical course	Progressive	true	Inferred relationship	Existential restriction modifier	3

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
378286012	Osteopetrosis - intermediate type	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
644969017	Osteopetrosis - intermediate type (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module