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1187515001: Mitochondrial phosphate carrier deficiency (disorder)


Status: current, Primitive. Date: 31-Jan 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4674059019 Mitochondrial phosphate carrier deficiency en Synonym Active Case insensitive SNOMED CT core
4674060012 Mitochondrial phosphate carrier deficiency (disorder) en Fully specified name Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Mitochondrial phosphate carrier deficiency Is a Mitochondrial metabolism defect true Inferred relationship Some
Mitochondrial phosphate carrier deficiency Is a Autosomal recessive hereditary disorder true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Clinical finding foundation reference set

Problem/Diagnosis reference set

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