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717767009: Alport syndrome autosomal recessive (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3310202018 Alport syndrome autosomal recessive (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3312046012 Alport syndrome autosomal recessive 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
Alport syndrome autosomal recessive Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Alport syndrome autosomal recessive Is a Hereditary nephritis false Inferred relationship Existential restriction modifier
Alport syndrome autosomal recessive Associated morphology Chronic inflammation true Inferred relationship Existential restriction modifier 1
Alport syndrome autosomal recessive Finding site Glomerulus structure true Inferred relationship Existential restriction modifier 1
Alport syndrome autosomal recessive Finding site Structure of auditory system true Inferred relationship Existential restriction modifier 3
Alport syndrome autosomal recessive Is a Alport syndrome true Inferred relationship Existential restriction modifier
Alport syndrome autosomal recessive Interprets Hearing, function 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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