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733091002: paralysie faciale congénitale héréditaire isolée (trouble)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3498731014 Isolated hereditary congenital facial paralysis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3498732019 Isolated hereditary congenital facial paralysis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
762921000241110 paralysie faciale congénitale héréditaire isolée (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
900381000172110 paralysie faciale congénitale héréditaire isolée fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
3499970018 An extremely rare neurological disorder presumed to result from maldevelopment of the facial nucleus and/or cranial nerve 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. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Isolated hereditary congenital facial paralysis (disorder) survenue (attribut) congénital true Inferred relationship Some 1
Isolated hereditary congenital facial paralysis (disorder) morphologie associée (attribut) Aplasia true Inferred relationship Some 1
Isolated hereditary congenital facial paralysis (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Isolated hereditary congenital facial paralysis (disorder) localisation d'une constatation (attribut) Facial nerve structure true Inferred relationship Some 1
Isolated hereditary congenital facial paralysis (disorder) est un(e) (attribut) Congenital anomaly of nervous system of head/neck true Inferred relationship Some
Isolated hereditary congenital facial paralysis (disorder) interprète (attribut) Movement (observable entity) true Inferred relationship Some 3
Isolated hereditary congenital facial paralysis (disorder) est un(e) (attribut) Developmental hereditary disorder true Inferred relationship Some
Isolated hereditary congenital facial paralysis (disorder) est un(e) (attribut) Autosomal hereditary disorder true Inferred relationship Some
Isolated hereditary congenital facial paralysis (disorder) est un(e) (attribut) Congenital anomaly of peripheral nerve true Inferred relationship Some
Isolated hereditary congenital facial paralysis (disorder) est un(e) (attribut) Congenital facial nerve palsy true Inferred relationship Some
Isolated hereditary congenital facial paralysis (disorder) est un(e) (attribut) Hereditary disorder of nervous system true Inferred relationship Some
Isolated hereditary congenital facial paralysis (disorder) a pour interprétation (attribut) Absent true Inferred relationship Some 2
Isolated hereditary congenital facial paralysis (disorder) interprète (attribut) mobilité globale du tronc et des membres true Inferred relationship Some 2
Isolated hereditary congenital facial paralysis (disorder) morphologie associée (attribut) Aplasia false Inferred relationship Some 3
Isolated hereditary congenital facial paralysis (disorder) survenue (attribut) congénital false Inferred relationship Some 3
Isolated hereditary congenital facial paralysis (disorder) localisation d'une constatation (attribut) Facial nerve structure false Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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