722109008: Osteocraniostenosis (disorder)

SNOMED CT Concept\Clinical finding\...

\Musculoskeletal finding\Bone finding\Disorder of bone\Disorder of bone development\Congenital anomaly of skeletal bone\Osteocraniostenosis
\Musculoskeletal finding\Disorder of musculoskeletal system\Hereditary disorder of musculoskeletal system\Osteocraniostenosis
\Musculoskeletal finding\Disorder of musculoskeletal system\Disorder of skeletal system\Congenital skeletal dysplasia\Osteocraniostenosis
\Musculoskeletal finding\Disorder of musculoskeletal system\Disorder of skeletal system\Disorder of bone\Disorder of bone development\Congenital anomaly of skeletal bone\Osteocraniostenosis
\Musculoskeletal finding\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Osteocraniostenosis
\Musculoskeletal finding\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Osteocraniostenosis

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Osteocraniostenosis
\Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Osteocraniostenosis
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Osteocraniostenosis
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Osteocraniostenosis
\Disease\Disorder of body system\Disorder of musculoskeletal system\Hereditary disorder of musculoskeletal system\Osteocraniostenosis
\Disease\Disorder of body system\Disorder of musculoskeletal system\Disorder of skeletal system\Congenital skeletal dysplasia\Osteocraniostenosis
\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\Osteocraniostenosis
\Disease\Disorder of body system\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Osteocraniostenosis
\Disease\Disorder of body system\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Osteocraniostenosis
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Osteocraniostenosis
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Osteocraniostenosis
\Disease\Developmental disorder\Disorder of bone development\Congenital anomaly of skeletal bone\Osteocraniostenosis
\Disease\Developmental disorder\Developmental hereditary disorder\Osteocraniostenosis
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Osteocraniostenosis
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Osteocraniostenosis

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

3330725011 Osteocraniostenosis (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

3330726012 Osteocraniostenosis en Synonym Active Entire term case insensitive SNOMED CT core module

3330727015 Gracile bone dysplasia en Synonym Active Entire term case insensitive SNOMED CT core module

3330728013 Osteocraniosplenic syndrome en Synonym Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Osteocraniostenosis	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Existential restriction modifier
Osteocraniostenosis	Is a	Congenital skeletal dysplasia	true	Inferred relationship	Existential restriction modifier
Osteocraniostenosis	Is a	Connective tissue hereditary disorder	false	Inferred relationship	Existential restriction modifier
Osteocraniostenosis	Is a	Hereditary disorder of musculoskeletal system	true	Inferred relationship	Existential restriction modifier
Osteocraniostenosis	Associated morphology	Congenital dysplasia	false	Inferred relationship	Existential restriction modifier	1
Osteocraniostenosis	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Osteocraniostenosis	Finding site	Bone structure	true	Inferred relationship	Existential restriction modifier	1
Osteocraniostenosis	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	1
Osteocraniostenosis	Associated morphology	Dysplasia	true	Inferred relationship	Existential restriction modifier	1
Osteocraniostenosis	Is a	Congenital anomaly of skeletal bone	true	Inferred relationship	Existential restriction modifier
Osteocraniostenosis	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
3330725011	Osteocraniostenosis (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
3330726012	Osteocraniostenosis	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3330727015	Gracile bone dysplasia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3330728013	Osteocraniosplenic syndrome	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module