230542008: Congenital facial nerve palsy (disorder)

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

\Finding of movement\Movement disorder\Facial palsy\Congenital facial nerve palsy
\Finding of movement\Motor dysfunction\Paralysis (finding)\Facial palsy\Congenital facial nerve palsy

\General finding of soft tissue\Peripheral nerve finding\Peripheral nerve disease\Facial nerve disorder (disorder)\Facial palsy\Congenital facial nerve palsy
\General finding of soft tissue\Peripheral nerve finding\Peripheral nerve disease\Facial nerve disorder (disorder)\Congenital disorder of facial nerve\Congenital facial nerve palsy
\General finding of soft tissue\Peripheral nerve finding\Seventh cranial nerve finding (finding)\Facial palsy\Congenital facial nerve palsy
\General finding of soft tissue\Disorder of soft tissue\Peripheral nerve disease\Facial nerve disorder (disorder)\Facial palsy\Congenital facial nerve palsy
\General finding of soft tissue\Disorder of soft tissue\Peripheral nerve disease\Facial nerve disorder (disorder)\Congenital disorder of facial nerve\Congenital facial nerve palsy

\Neurological finding\Cranial nerve finding\Seventh cranial nerve finding (finding)\Facial palsy\Congenital facial nerve palsy
\Neurological finding\Motor nervous system finding (finding)\Motor dysfunction\Paralysis (finding)\Facial palsy\Congenital facial nerve palsy

\Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital disorder of facial nerve\Congenital facial nerve palsy
\Disease\Disorder of body system\Disease of nervous system (disorder)\Neuropathy\Peripheral nerve disease\Facial nerve disorder (disorder)\Facial palsy\Congenital facial nerve palsy
\Disease\Disorder of body system\Disease of nervous system (disorder)\Neuropathy\Peripheral nerve disease\Facial nerve disorder (disorder)\Congenital disorder of facial nerve\Congenital facial nerve palsy
\Disease\Disorder of body system\Disease of nervous system (disorder)\Neuropathy\Cranial nerve disorder (disorder)\Facial nerve disorder (disorder)\Facial palsy\Congenital facial nerve palsy
\Disease\Disorder of body system\Disease of nervous system (disorder)\Neuropathy\Cranial nerve disorder (disorder)\Facial nerve disorder (disorder)\Congenital disorder of facial nerve\Congenital facial nerve palsy
\Disease\Disorder of body system\Disease of nervous system (disorder)\Disorder of the peripheral nervous system (disorder)\Peripheral nerve disease\Facial nerve disorder (disorder)\Facial palsy\Congenital facial nerve palsy
\Disease\Disorder of body system\Disease of nervous system (disorder)\Disorder of the peripheral nervous system (disorder)\Peripheral nerve disease\Facial nerve disorder (disorder)\Congenital disorder of facial nerve\Congenital facial nerve palsy
\Disease\Movement disorder\Facial palsy\Congenital facial nerve palsy
\Disease\Disorder of soft tissue\Peripheral nerve disease\Facial nerve disorder (disorder)\Facial palsy\Congenital facial nerve palsy
\Disease\Disorder of soft tissue\Peripheral nerve disease\Facial nerve disorder (disorder)\Congenital disorder of facial nerve\Congenital facial nerve palsy

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 facial nerve palsy	Is a	Peripheral nerve facial nerve paralysis	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital facial nerve palsy	Is a	Congenital disorder of facial nerve	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital facial nerve palsy	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital facial nerve palsy	Finding site	Facial nerve structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital facial nerve palsy	Is a	Facial palsy	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital facial nerve palsy	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital facial nerve palsy	Finding site	Facial nerve structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital facial nerve palsy	Has interpretation	Absent	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital facial nerve palsy	Interprets	Gross movement of body and limbs (observable entity)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital facial nerve palsy	Interprets	Movement	true	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Congenital facial nerve palsy	Interprets	Movement observable	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Facial palsy as birth trauma	Is a	False	Congenital facial nerve palsy	Inferred relationship	Existential restriction modifier (core metadata concept)
Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome (disorder)	Is a	True	Congenital facial nerve palsy	Inferred relationship	Existential restriction modifier (core metadata concept)
Isolated hereditary congenital facial paralysis (IHCFP) is an extremely rare neurological disorder presumed to result from maldevelopment of the facial nucleus and/or cranial nerve and has been reported in fewer than 10 families to date. It manifests as non-progressive, isolated, unilateral or bilateral, symmetrical or asymmetrical facial palsy. Involvement of the branches of the facial nerve can be unequal.	Is a	True	Congenital facial nerve palsy	Inferred relationship	Existential restriction modifier (core metadata concept)
Moebius syndrome (disorder)	Is a	True	Congenital facial nerve palsy	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
345448013	Congenital facial nerve palsy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
618364017	Congenital facial nerve palsy (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
345448013	Congenital facial nerve palsy	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
345448013	Congenital facial nerve palsy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
618364017	Congenital facial nerve palsy (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
618364017	Congenital facial nerve palsy (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4959801000241112	paralysie congénitale du nerf facial	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
4959801000241112	paralysie congénitale du nerf facial	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module