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1003387003: Molybdenum cofactor deficiency complementation group C (disorder)


Status: current, Primitive. Date: 31-Jan 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4168135014 Molybdenum cofactor deficiency complementation group C en Synonym Active Initial character case insensitive SNOMED CT core
4168136010 Molybdenum cofactor deficiency complementation group C (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core
4167394016 A subtype of molybdenum cofactor deficiency caused by GPHN gene mutation. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Molybdenum cofactor deficiency complementation group C Is a Combined molybdoflavoprotein enzyme deficiency 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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