717221005: Metaphyseal dysplasia Braun Tinschert type (disorder)

SNOMED CT Concept\Clinical finding\...

\Evaluation finding\Imaging finding\Bone densimetry abnormal\Bone density above reference range\Dysplasia with increased bone density\Metaphyseal dysplasia Braun Tinschert type

\General finding of observation of patient\Procedure related finding\Bone density finding\Bone density above reference range\Dysplasia with increased bone density\Metaphyseal dysplasia Braun Tinschert type

\Musculoskeletal finding\Bone finding\Bone density finding\Bone density above reference range\Dysplasia with increased bone density\Metaphyseal dysplasia Braun Tinschert type
\Musculoskeletal finding\Bone finding\Disorder of bone\Disorder of bone development\Congenital anomaly of skeletal bone\Metaphyseal dysplasia Braun Tinschert type
\Musculoskeletal finding\Bone finding\Disorder of bone\Dysplasia with increased bone density\Metaphyseal dysplasia Braun Tinschert type
\Musculoskeletal finding\Disorder of musculoskeletal system\Hereditary disorder of musculoskeletal system\Metaphyseal dysplasia Braun Tinschert type
\Musculoskeletal finding\Disorder of musculoskeletal system\Disorder of skeletal system\Congenital skeletal dysplasia\Dysplasia with increased bone density\Metaphyseal dysplasia Braun Tinschert type
\Musculoskeletal finding\Disorder of musculoskeletal system\Disorder of skeletal system\Disorder of bone\Disorder of bone development\Congenital anomaly of skeletal bone\Metaphyseal dysplasia Braun Tinschert type
\Musculoskeletal finding\Disorder of musculoskeletal system\Disorder of skeletal system\Disorder of bone\Dysplasia with increased bone density\Metaphyseal dysplasia Braun Tinschert type
\Musculoskeletal finding\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Dysplasia with increased bone density\Metaphyseal dysplasia Braun Tinschert type
\Musculoskeletal finding\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Metaphyseal dysplasia Braun Tinschert type

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Metaphyseal dysplasia Braun Tinschert type
\Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Metaphyseal dysplasia Braun Tinschert type
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Metaphyseal dysplasia Braun Tinschert type
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Metaphyseal dysplasia Braun Tinschert type
\Disease\Disorder of body system\Disorder of musculoskeletal system\Hereditary disorder of musculoskeletal system\Metaphyseal dysplasia Braun Tinschert type
\Disease\Disorder of body system\Disorder of musculoskeletal system\Disorder of skeletal system\Congenital skeletal dysplasia\Dysplasia with increased bone density\Metaphyseal dysplasia Braun Tinschert 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\Metaphyseal dysplasia Braun Tinschert type
\Disease\Disorder of body system\Disorder of musculoskeletal system\Disorder of skeletal system\Disorder of bone\Dysplasia with increased bone density\Metaphyseal dysplasia Braun Tinschert type
\Disease\Disorder of body system\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Dysplasia with increased bone density\Metaphyseal dysplasia Braun Tinschert type
\Disease\Disorder of body system\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Metaphyseal dysplasia Braun Tinschert type
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Dysplasia with increased bone density\Metaphyseal dysplasia Braun Tinschert type
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Metaphyseal dysplasia Braun Tinschert type
\Disease\Developmental disorder\Disorder of bone development\Congenital anomaly of skeletal bone\Metaphyseal dysplasia Braun Tinschert type
\Disease\Developmental disorder\Developmental hereditary disorder\Metaphyseal dysplasia Braun Tinschert type
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Dysplasia with increased bone density\Metaphyseal dysplasia Braun Tinschert type
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Metaphyseal dysplasia Braun Tinschert type

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2016. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

3308711010 Metaphyseal dysplasia Braun Tinschert type (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module

3308712015 Metaphyseal dysplasia Braun Tinschert type en Synonym Active Only initial character case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Metaphyseal dysplasia Braun Tinschert type	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Existential restriction modifier
Metaphyseal dysplasia Braun Tinschert type	Is a	Dysplasia with increased bone density	true	Inferred relationship	Existential restriction modifier
Metaphyseal dysplasia Braun Tinschert type	Is a	Connective tissue hereditary disorder	false	Inferred relationship	Existential restriction modifier
Metaphyseal dysplasia Braun Tinschert type	Is a	Hereditary disorder of musculoskeletal system	true	Inferred relationship	Existential restriction modifier
Metaphyseal dysplasia Braun Tinschert type	Associated morphology	Congenital dysplasia	false	Inferred relationship	Existential restriction modifier	2
Metaphyseal dysplasia Braun Tinschert type	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier	2
Metaphyseal dysplasia Braun Tinschert type	Finding site	Bone structure	false	Inferred relationship	Existential restriction modifier	2
Metaphyseal dysplasia Braun Tinschert type	Finding site	Bone structure	true	Inferred relationship	Existential restriction modifier	1
Metaphyseal dysplasia Braun Tinschert type	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Metaphyseal dysplasia Braun Tinschert type	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	1
Metaphyseal dysplasia Braun Tinschert type	Associated morphology	Congenital dysplasia	false	Inferred relationship	Existential restriction modifier	1
Metaphyseal dysplasia Braun Tinschert type	Associated morphology	Dysplasia	true	Inferred relationship	Existential restriction modifier	1
Metaphyseal dysplasia Braun Tinschert type	Interprets	Bone density scan	true	Inferred relationship	Existential restriction modifier	2
Metaphyseal dysplasia Braun Tinschert type	Has interpretation	Above reference range	true	Inferred relationship	Existential restriction modifier	2
Metaphyseal dysplasia Braun Tinschert type	Is a	Congenital anomaly of skeletal bone	true	Inferred relationship	Existential restriction modifier
Metaphyseal dysplasia Braun Tinschert type	Is a	Developmental hereditary disorder	true	Inferred relationship	Existential restriction modifier

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
3308711010	Metaphyseal dysplasia Braun Tinschert type (disorder)	en	Fully specified name	Active	Only initial character case insensitive	SNOMED CT core module
3308712015	Metaphyseal dysplasia Braun Tinschert type	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module