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80473005: Neonatal hyperhistidinemia (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
133535014 Neonatal hyperhistidinemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
504435014 Neonatal hyperhistidinaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
821637019 Neonatal hyperhistidinemia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
133535014 Neonatal hyperhistidinemia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
133535014 Neonatal hyperhistidinemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
504435014 Neonatal hyperhistidinaemia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
504435014 Neonatal hyperhistidinaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
821637019 Neonatal hyperhistidinemia (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
821637019 Neonatal hyperhistidinemia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4653451000241113 hyperhistidinémie néonatale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4653451000241113 hyperhistidinémie néonatale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Neonatal hyperhistidinaemia Is a troubles endocriniens et/ou métaboliques spécifiques au fœtus ou au nouveau-né false Inferred relationship Existential restriction modifier (core metadata concept)
Neonatal hyperhistidinaemia Is a Hereditary disorder of endocrine system (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Neonatal hyperhistidinaemia Is a Congenital anomaly of endocrine gland false Inferred relationship Existential restriction modifier (core metadata concept)
Neonatal hyperhistidinaemia Is a Disorder of histidine metabolism true Inferred relationship Existential restriction modifier (core metadata concept)
Neonatal hyperhistidinaemia Is a Reproductive system hereditary disorder (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Neonatal hyperhistidinaemia Finding site Entire endocrine gonad (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Neonatal hyperhistidinaemia Occurrence Neonatal false Inferred relationship Existential restriction modifier (core metadata concept)
Neonatal hyperhistidinaemia Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Neonatal hyperhistidinaemia Finding site Body system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Neonatal hyperhistidinaemia Is a Neonatal disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Neonatal hyperhistidinaemia Occurrence Neonatal true Inferred relationship Existential restriction modifier (core metadata concept) 1
Neonatal hyperhistidinaemia Is a Neonatal metabolic disorder (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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