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297255007: Hepatic glycogen phosphorylase kinase deficiency (disorder)


Status: current. Date: 31-Jan 2002

Descriptions:

Id Description Lang Type Status Case? Module
437744011 Hepatic glycogen phosphorylase kinase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
692567011 Hepatic glycogen phosphorylase kinase deficiency (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hepatic glycogen phosphorylase kinase deficiency Is a Glycogen phosphorylase kinase deficiency, autosomal recessive true Congenital syphilitic hepatomegaly Congenital syphilitic hepatomegaly
Hepatic glycogen phosphorylase kinase deficiency Occurrence Congenital true Congenital syphilitic hepatomegaly Congenital syphilitic hepatomegaly 1
Hepatic glycogen phosphorylase kinase deficiency Finding site Liver structure true Congenital syphilitic hepatomegaly Congenital syphilitic hepatomegaly 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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