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721225009: Homocystinuria without methylmalonic aciduria (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
3324669011 Homocystinuria without methylmalonic aciduria (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3324671011 Homocystinuria without methylmalonic aciduria en Synonym Active Entire term case insensitive SNOMED CT core module
3324672016 Functional methionine synthase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Homocystinuria without methylmalonic aciduria Is a Homocystinuria true Inferred relationship Existential restriction modifier
Homocystinuria without methylmalonic aciduria Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Homocystinuria without methylmalonic aciduria Is a Functional defects of methionine synthase true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group
Methylcobalamin deficiency type cbl G Is a True Homocystinuria without methylmalonic aciduria Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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