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721173005: Hypotonia cystinuria syndrome (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
3324522011 Hypotonia cystinuria syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3324523018 Hypotonia cystinuria syndrome 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
Hypotonia cystinuria syndrome Is a Amino acid transport disorder false Inferred relationship Existential restriction modifier
Hypotonia cystinuria syndrome Is a Autosomal recessive hereditary disorder false Inferred relationship Existential restriction modifier
Hypotonia cystinuria syndrome Interprets Muscle tone true Inferred relationship Existential restriction modifier 3
Hypotonia cystinuria syndrome Is a Cystinuria, type 1 true Inferred relationship Existential restriction modifier
Hypotonia cystinuria syndrome Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier 1
Hypotonia cystinuria syndrome Finding site Kidney structure 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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