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1187514002: Myopathic form of carnitine palmitoyltransferase II deficiency (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2022. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
4674057017 Myopathic form of carnitine palmitoyltransferase II deficiency en Synonym Active Only initial character case insensitive SNOMED CT core module
4674058010 Myopathic form of carnitine palmitoyltransferase II deficiency (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Myopathic form of carnitine palmitoyltransferase II deficiency Is a Carnitine palmitoyltransferase II deficiency true Inferred relationship Existential restriction modifier
Myopathic form of carnitine palmitoyltransferase II deficiency Occurrence Congenital true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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