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733091002: Isolated hereditary congenital facial paralysis (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3498731014 Isolated hereditary congenital facial paralysis (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3498732019 Isolated hereditary congenital facial paralysis en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Isolated hereditary congenital facial paralysis Is a Autosomal hereditary disorder true Inferred relationship Existential restriction modifier
Isolated hereditary congenital facial paralysis Is a Congenital anomaly of peripheral nerve true Inferred relationship Existential restriction modifier
Isolated hereditary congenital facial paralysis Is a Congenital facial nerve palsy true Inferred relationship Existential restriction modifier
Isolated hereditary congenital facial paralysis Is a Hereditary disorder of nervous system true Inferred relationship Existential restriction modifier
Isolated hereditary congenital facial paralysis Has interpretation Absent true Inferred relationship Existential restriction modifier 2
Isolated hereditary congenital facial paralysis Interprets Gross movement of body and limbs false Inferred relationship Existential restriction modifier 2
Isolated hereditary congenital facial paralysis Associated morphology Aplasia false Inferred relationship Existential restriction modifier 3
Isolated hereditary congenital facial paralysis Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Isolated hereditary congenital facial paralysis Finding site Facial nerve structure false Inferred relationship Existential restriction modifier 3
Isolated hereditary congenital facial paralysis Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Isolated hereditary congenital facial paralysis Associated morphology Aplasia true Inferred relationship Existential restriction modifier 1
Isolated hereditary congenital facial paralysis Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Isolated hereditary congenital facial paralysis Finding site Facial nerve structure true Inferred relationship Existential restriction modifier 1
Isolated hereditary congenital facial paralysis Is a Congenital anomaly of nervous system of head/neck true Inferred relationship Existential restriction modifier
Isolated hereditary congenital facial paralysis Interprets Movement true Inferred relationship Existential restriction modifier 3
Isolated hereditary congenital facial paralysis Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Isolated hereditary congenital facial paralysis Interprets Movement observable true Inferred relationship Existential restriction modifier 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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