93244008: Congenital hypoplasia of basisphenoid bone (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Head finding (finding)\Disorder of head (disorder)\Congenital anomaly of head\Congenital anomaly of fetal head bones\Congenital anomaly of basisphenoid bone\Congenital hypoplasia of basisphenoid bone

\Musculoskeletal finding (finding)\Bone finding\Disorder of bone (disorder)\Disorder of bone development\Congenital anomaly of skeletal bone\Congenital anomaly of fetal head bones\Congenital anomaly of basisphenoid bone\Congenital hypoplasia of basisphenoid bone
\Musculoskeletal finding (finding)\Disorder of musculoskeletal system (disorder)\Disorder of skeletal system\Disorder of bone (disorder)\Disorder of bone development\Congenital anomaly of skeletal bone\Congenital anomaly of fetal head bones\Congenital anomaly of basisphenoid bone\Congenital hypoplasia of basisphenoid bone
\Musculoskeletal finding (finding)\Disorder of musculoskeletal system (disorder)\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Congenital anomaly of fetal head bones\Congenital anomaly of basisphenoid bone\Congenital hypoplasia of basisphenoid bone

\Disease\Disorder of embryonic structure (disorder)\Congenital anomaly of fetal head bones\Congenital anomaly of basisphenoid bone\Congenital hypoplasia of basisphenoid bone
\Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital malformation\Congenital anomaly of head\Congenital anomaly of fetal head bones\Congenital anomaly of basisphenoid bone\Congenital hypoplasia of basisphenoid bone
\Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Congenital anomaly of fetal head bones\Congenital anomaly of basisphenoid bone\Congenital hypoplasia of basisphenoid bone
\Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Disorder of skeletal system\Disorder of bone (disorder)\Disorder of bone development\Congenital anomaly of skeletal bone\Congenital anomaly of fetal head bones\Congenital anomaly of basisphenoid bone\Congenital hypoplasia of basisphenoid bone
\Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Congenital anomaly of fetal head bones\Congenital anomaly of basisphenoid bone\Congenital hypoplasia of basisphenoid bone
\Disease\Disorder of head (disorder)\Congenital anomaly of head\Congenital anomaly of fetal head bones\Congenital anomaly of basisphenoid bone\Congenital hypoplasia of basisphenoid bone
\Disease\Developmental disorder (disorder)\Disorder of bone development\Congenital anomaly of skeletal bone\Congenital anomaly of fetal head bones\Congenital anomaly of basisphenoid bone\Congenital hypoplasia of basisphenoid bone
\Disease\Developmental disorder (disorder)\Congenital malformation\Congenital anomaly of head\Congenital anomaly of fetal head bones\Congenital anomaly of basisphenoid bone\Congenital hypoplasia of basisphenoid bone
\Disease\Developmental disorder (disorder)\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Congenital anomaly of fetal head bones\Congenital anomaly of basisphenoid bone\Congenital hypoplasia of basisphenoid bone

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Congenital hypoplasia of basisphenoid bone	Is a	Congenital anomaly of basisphenoid bone	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital hypoplasia of basisphenoid bone	Associated morphology	Congenital hypoplasia	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital hypoplasia of basisphenoid bone	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital hypoplasia of basisphenoid bone	Finding site	Structure of basisphenoid bone (body structure)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital hypoplasia of basisphenoid bone	Finding site	Bone structure of cranium	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital hypoplasia of basisphenoid bone	Is a	Congenital malformation	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital hypoplasia of basisphenoid bone	Finding site	Structure of basisphenoid bone (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital hypoplasia of basisphenoid bone	Finding site	Bone structure of cranium	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital hypoplasia of basisphenoid bone	Associated morphology	Congenital hypoplasia	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital hypoplasia of basisphenoid bone	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital hypoplasia of basisphenoid bone	Finding site	Structure of basisphenoid bone (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital hypoplasia of basisphenoid bone	Associated morphology	Hypoplasia	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital hypoplasia of basisphenoid bone	Associated morphology	Hypoplasia	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital hypoplasia of basisphenoid bone	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital hypoplasia of basisphenoid bone	Pathological process (attribute)	Pathological developmental process (qualifier value)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
154277011	Congenital hypoplasia of basisphenoid bone	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
154278018	Congenital small basisphenoid bone	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
836937012	Congenital hypoplasia of basisphenoid bone (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
154277011	Congenital hypoplasia of basisphenoid bone	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
154277011	Congenital hypoplasia of basisphenoid bone	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
154278018	Congenital small basisphenoid bone	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
154278018	Congenital small basisphenoid bone	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
836937012	Congenital hypoplasia of basisphenoid bone (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
836937012	Congenital hypoplasia of basisphenoid bone (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4708571000241114	hypoplasie congénitale de la partie basilaire de l'os sphénoïde	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
4708571000241114	hypoplasie congénitale de la partie basilaire de l'os sphénoïde	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module