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733091002: Isolated hereditary congenital facial paralysis (disorder)


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
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) Is a Autosomal hereditary disorder true Inferred relationship Some
Isolated hereditary congenital facial paralysis (disorder) Is a Congenital anomaly of peripheral nerve true Inferred relationship Some
Isolated hereditary congenital facial paralysis (disorder) Is a Congenital facial nerve palsy (disorder) true Inferred relationship Some
Isolated hereditary congenital facial paralysis (disorder) Is a Hereditary disorder of nervous system true Inferred relationship Some
Isolated hereditary congenital facial paralysis (disorder) Has interpretation Absent true Inferred relationship Some 2
Isolated hereditary congenital facial paralysis (disorder) Interprets Gross movement of body and limbs false Inferred relationship Some 2
Isolated hereditary congenital facial paralysis (disorder) Associated morphology Aplasia false Inferred relationship Some 3
Isolated hereditary congenital facial paralysis (disorder) Occurrence Congenital false Inferred relationship Some 3
Isolated hereditary congenital facial paralysis (disorder) Finding site Facial nerve structure false Inferred relationship Some 3
Isolated hereditary congenital facial paralysis (disorder) Occurrence Congenital true Inferred relationship Some 1
Isolated hereditary congenital facial paralysis (disorder) Associated morphology 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) Finding site Facial nerve structure true Inferred relationship Some 1
Isolated hereditary congenital facial paralysis (disorder) Is a Congenital anomaly of nervous system of head/neck (disorder) true Inferred relationship Some
Isolated hereditary congenital facial paralysis (disorder) Interprets Movement true Inferred relationship Some 3
Isolated hereditary congenital facial paralysis (disorder) Is a Developmental hereditary disorder true Inferred relationship Some
Isolated hereditary congenital facial paralysis (disorder) Interprets Movement observable true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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