49557009: Pontine structure (body structure)

SNOMED CT Concept\Body structure\Anatomical or acquired body structure (body structure)\Anatomical structure\...

\Structure of anatomical cluster (body structure)\Structure of anatomical compartment (body structure)\Intracranial structure\Brain structure\Brain part\Brain region\Infratentorial brain structure\Infratentorial brain part\Brainstem structure\Brain stem part (body structure)\Midbrain and pons structure\Pontine structure

\Body organ structure\Brain and spinal cord structure (body structure)\Brain structure\Brain part\Brain region\Infratentorial brain structure\Infratentorial brain part\Brainstem structure\Brain stem part (body structure)\Midbrain and pons structure\Pontine structure
\Body organ structure\Organ part (body structure)\Brain part\Brain region\Infratentorial brain structure\Infratentorial brain part\Brainstem structure\Brain stem part (body structure)\Midbrain and pons structure\Pontine structure

\Body region structure\Body part structure\Upper body structure\Upper body part structure\Structure of head and/or neck (body structure)\Head structure (body structure)\Head part\Intracranial structure\Brain structure\Brain part\Brain region\Infratentorial brain structure\Infratentorial brain part\Brainstem structure\Brain stem part (body structure)\Midbrain and pons structure\Pontine structure

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

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Pontine structure	Is a	Midbrain and pons structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Pontine structure	Is a	Hindbrain structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Pontine structure	partie de	Entire midbrain and pons	false	Additional relationship (core metadata concept)	Existential restriction modifier (core metadata concept)

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Entire pons	Is a	True	Pontine structure	Inferred relationship	Existential restriction modifier (core metadata concept)
Pontine nucleus (body structure)	Is a	False	Pontine structure	Inferred relationship	Existential restriction modifier (core metadata concept)
Pons part	Is a	True	Pontine structure	Inferred relationship	Existential restriction modifier (core metadata concept)
Pontine tract	Is a	False	Pontine structure	Inferred relationship	Existential restriction modifier (core metadata concept)
Tegmental pons	Is a	False	Pontine structure	Inferred relationship	Existential restriction modifier (core metadata concept)
Ventral pons	Is a	False	Pontine structure	Inferred relationship	Existential restriction modifier (core metadata concept)
Structure of cerebellopontine angle	Is a	False	Pontine structure	Inferred relationship	Existential restriction modifier (core metadata concept)
Structure of median eminence of pons	Is a	False	Pontine structure	Inferred relationship	Existential restriction modifier (core metadata concept)
Structure of isthmus of rhombencephalon	Is a	False	Pontine structure	Inferred relationship	Existential restriction modifier (core metadata concept)
Structure of tegmentum of rhombencephalon (body structure)	Is a	False	Pontine structure	Inferred relationship	Existential restriction modifier (core metadata concept)
Rhomboid fossa structure	Is a	False	Pontine structure	Inferred relationship	Existential restriction modifier (core metadata concept)
Malignant neoplasm of pons	Finding site	False	Pontine structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Foville's syndrome I	Finding site	False	Pontine structure	Inferred relationship	Existential restriction modifier (core metadata concept)
Nuclear facial nerve paralysis	Finding site	True	Pontine structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital pontocerebellar hypoplasia	Finding site	False	Pontine structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Foville-Wilson syndrome	Finding site	False	Pontine structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Central pontine myelinolysis	Finding site	False	Pontine structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Foville's syndrome II	Finding site	False	Pontine structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Intrapontine haemorrhage	Finding site	False	Pontine structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Pontine one and a half syndrome	Finding site	True	Pontine structure	Inferred relationship	Existential restriction modifier (core metadata concept)	2
tumeur bénigne du pont cerebral	Finding site	False	Pontine structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital pontocerebellar hypoplasia	Finding site	False	Pontine structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Central pontine myelinolysis	Finding site	True	Pontine structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Intrapontine haemorrhage	Finding site	True	Pontine structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
tumeur bénigne du pont cerebral	Finding site	True	Pontine structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Malignant neoplasm of pons	Finding site	True	Pontine structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Foville's syndrome II	Finding site	False	Pontine structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Foville's syndrome II	Finding site	False	Pontine structure	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Congenital pontocerebellar hypoplasia	Finding site	True	Pontine structure	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital pontocerebellar hypoplasia	Finding site	False	Pontine structure	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Congenital pontocerebellar hypoplasia type 2 (disorder)	Finding site	True	Pontine structure	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital pontocerebellar hypoplasia type 7 (disorder)	Finding site	False	Pontine structure	Inferred relationship	Existential restriction modifier (core metadata concept)	2
A rare, genetic form of pontocerebellar hypoplasia (PCH) characterized by neocortical and severe cerebral cortical atrophy associated with pontocerebellar hypoplasia with the pons and cerebellum equally affected. Clinically the disorder manifests at birth with hypotonia, clonus, epilepsy, impaired swallowing and from infancy by progressive microcephaly, spasticity and lactic acidosis.	Finding site	False	Pontine structure	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital pontocerebellar hypoplasia type 5	Finding site	False	Pontine structure	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital pontocerebellar hypoplasia type 4 (disorder)	Finding site	True	Pontine structure	Inferred relationship	Existential restriction modifier (core metadata concept)	2
A rare, genetic form of pontocerebellar hypoplasia (PCH) characterised by neocortical and pontocerebellar hypoplasia with pons and cerebellum equally affected and that clinically manifests with neonatal hypotonia and impaired swallowing followed by seizures, optic atrophy and short stature from infancy onward. Movement disorders, as seen in other forms of PCH, are absent.	Finding site	False	Pontine structure	Inferred relationship	Existential restriction modifier (core metadata concept)	2
A severe, genetic form of pontocerebellar hypoplasia (PCH) characterized by spinal cord anterior horn cell degeneration in addition to pontocerebellar hypoplasia. Clinically, patients manifest with a severe global development deficit that is evident early on from difficulties in feeding and swallowing.	Finding site	False	Pontine structure	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital pontocerebellar hypoplasia type 8 (disorder)	Finding site	False	Pontine structure	Inferred relationship	Existential restriction modifier (core metadata concept)	2
A rare, genetic form of pontocerebellar hypoplasia (PCH) characterised by neocortical and pontocerebellar hypoplasia with pons and cerebellum equally affected and that clinically manifests with neonatal hypotonia and impaired swallowing followed by seizures, optic atrophy and short stature from infancy onward. Movement disorders, as seen in other forms of PCH, are absent.	Finding site	True	Pontine structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
A severe, genetic form of pontocerebellar hypoplasia (PCH) characterized by spinal cord anterior horn cell degeneration in addition to pontocerebellar hypoplasia. Clinically, patients manifest with a severe global development deficit that is evident early on from difficulties in feeding and swallowing.	Finding site	True	Pontine structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital pontocerebellar hypoplasia type 8 (disorder)	Finding site	True	Pontine structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital pontocerebellar hypoplasia type 7 (disorder)	Finding site	True	Pontine structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
A rare, genetic form of pontocerebellar hypoplasia (PCH) characterized by neocortical and severe cerebral cortical atrophy associated with pontocerebellar hypoplasia with the pons and cerebellum equally affected. Clinically the disorder manifests at birth with hypotonia, clonus, epilepsy, impaired swallowing and from infancy by progressive microcephaly, spasticity and lactic acidosis.	Finding site	True	Pontine structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital pontocerebellar hypoplasia type 5	Finding site	True	Pontine structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital pontocerebellar hypoplasia type 9 (disorder)	Finding site	True	Pontine structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
A rare genetic pontocerebellar hypoplasia subtype with characteristics of severe psychomotor developmental delay, progressive microcephaly, progressive spasticity, seizures and brain abnormalities consisting of mild atrophy of the cerebellum, pons and corpus callosum and cortical atrophy with delayed myelination. Patients may present dysmorphic facial features (high arched eyebrows, prominent eyes, long palpebral fissures and eyelashes, broad nasal root and hypoplastic alae nasi) and an axonal sensorimotor neuropathy. Caused by homozygous mutation in the CLP1 gene on chromosome 11q12.	Finding site	True	Pontine structure	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation	Finding site	True	Pontine structure	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Abscess of pons cerebri (disorder)	Finding site	True	Pontine structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Diffuse intrinsic pontine glioma (disorder)	Finding site	True	Pontine structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Foville syndrome (disorder)	Finding site	True	Pontine structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Osmotic demyelination syndrome (disorder)	Finding site	True	Pontine structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Primary diffuse intrinsic pontine glioma (disorder)	Finding site	True	Pontine structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital pontocerebellar hypoplasia type 11 (disorder)	Finding site	True	Pontine structure	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Congenital pontocerebellar hypoplasia type 12	Finding site	True	Pontine structure	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Congenital pontocerebellar hypoplasia type 13	Finding site	True	Pontine structure	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital pontocerebellar hypoplasia type 14	Finding site	True	Pontine structure	Inferred relationship	Existential restriction modifier (core metadata concept)	3

Reference Sets

Anatomy structure and entire association reference set (foundation metadata concept)

Anatomy structure and part association reference set (foundation metadata concept)

Description inactivation indicator reference set

US English

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Id	Description	Lang	Type	Status	Case?	Module
82547014	Pons	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
82549012	Pons cerebri	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
495434011	Pontine structure	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
787248019	Pontine structure (body structure)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
82547014	Pons	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
82547014	Pons	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
82549012	Pons cerebri	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
82549012	Pons cerebri	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
495434011	Pontine structure	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
495434011	Pontine structure	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
787248019	Pontine structure (body structure)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
787248019	Pontine structure (body structure)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5650221000241119	pont	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5650231000241117	structure du pont	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5650221000241119	pont	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5650231000241117	structure du pont	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module