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61071003: Proline dehydrogenase deficiency (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
101484012 Proline dehydrogenase deficiency en Synonym Active Case insensitive SNOMED CT core
101485013 Hyperprolinemia, type I en Synonym Active Initial character case insensitive SNOMED CT core
101486014 Proline oxidase deficiency en Synonym Active Case insensitive SNOMED CT core
1216791011 Hyperprolinaemia type I en Synonym Active Initial character case insensitive SNOMED CT core
1218279011 Hyperprolinemia type I en Synonym Active Initial character case insensitive SNOMED CT core
498929018 Hyperprolinaemia, type I en Synonym Active Initial character case insensitive SNOMED CT core
800093016 Proline dehydrogenase 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
Proline dehydrogenase deficiency Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Proline dehydrogenase deficiency Is a Enzymopathy true Inferred relationship Some
Proline dehydrogenase deficiency Is a Hyperprolinaemia true Inferred relationship Some
Proline dehydrogenase deficiency Is a Inborn error of metabolism true Inferred relationship Some
Proline dehydrogenase deficiency Finding site Body system structure false Inferred relationship Some
Proline dehydrogenase deficiency Occurrence Congenital true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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