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253175003: Familial aplasia of the vermis (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
377069011 Familial aplasia of the vermis en Synonym Active Entire term case insensitive SNOMED CT core module
643903011 Familial aplasia of the vermis (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


7 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial aplasia of the vermis Is a Aplasia of the vermis true Inferred relationship Existential restriction modifier
Familial aplasia of the vermis Finding site Cerebellar vermis structure false Inferred relationship Existential restriction modifier 2
Familial aplasia of the vermis Occurrence Congenital false Inferred relationship Existential restriction modifier
Familial aplasia of the vermis Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Familial aplasia of the vermis Finding site Cerebellar structure false Inferred relationship Existential restriction modifier 1
Familial aplasia of the vermis Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
Familial aplasia of the vermis Finding site Structure of nervous system false Inferred relationship Existential restriction modifier 1
Familial aplasia of the vermis Finding site Cerebellar structure false Inferred relationship Existential restriction modifier 1
Familial aplasia of the vermis Associated morphology Congenital developmental anomaly false Inferred relationship Existential restriction modifier 1
Familial aplasia of the vermis Finding site Cerebellar structure false Inferred relationship Existential restriction modifier 1
Familial aplasia of the vermis Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Familial aplasia of the vermis Associated morphology Congenital developmental anomaly false Inferred relationship Existential restriction modifier 1
Familial aplasia of the vermis Finding site Cerebellar vermis structure false Inferred relationship Existential restriction modifier 1
Familial aplasia of the vermis Finding site Cerebellar vermis structure true Inferred relationship Existential restriction modifier 1
Familial aplasia of the vermis Associated morphology Congenital developmental anomaly false Inferred relationship Existential restriction modifier 1
Familial aplasia of the vermis Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Familial aplasia of the vermis Associated morphology Aplasia false Inferred relationship Existential restriction modifier 2
Familial aplasia of the vermis Finding site Cerebellar vermis structure false Inferred relationship Existential restriction modifier 2
Familial aplasia of the vermis Associated morphology Aplasia true Inferred relationship Existential restriction modifier 1
Familial aplasia of the vermis Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Familial aplasia of the vermis Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Joubert syndrome Is a True Familial aplasia of the vermis Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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