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6160004: Neonatal hemochromatosis (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2005. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
11239018 Neonatal hemochromatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
499062017 Idiopathic neonatal hemochromatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
499063010 Idiopathic neonatal haemochromatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
499064016 Neonatal haemochromatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
800680010 Neonatal hemochromatosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
11239018 Neonatal hemochromatosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
11239018 Neonatal hemochromatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
499061012 Neonatal giant cell hepatitis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
499062017 Idiopathic neonatal hemochromatosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
499062017 Idiopathic neonatal hemochromatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
499063010 Idiopathic neonatal haemochromatosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
499063010 Idiopathic neonatal haemochromatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
499064016 Neonatal haemochromatosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
499064016 Neonatal haemochromatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
800680010 Neonatal hemochromatosis (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
800680010 Neonatal hemochromatosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3389371001000117 Hämochromatose, neonatale de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
974361000172115 hémochromatose néonatale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
974361000172115 hémochromatose néonatale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3389371001000117 Hämochromatose, neonatale de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Neonatal hemochromatosis (disorder) Is a Perinatal hepatitis false Inferred relationship Existential restriction modifier (core metadata concept)
Neonatal hemochromatosis (disorder) Is a Hemochromatosis false Inferred relationship Existential restriction modifier (core metadata concept)
Neonatal hemochromatosis (disorder) Finding site Digestive system subdivision false Inferred relationship Existential restriction modifier (core metadata concept)
Neonatal hemochromatosis (disorder) Causative agent (attribute) Iron (substance) false Inferred relationship Existential restriction modifier (core metadata concept)
Neonatal hemochromatosis (disorder) Finding site Liver structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Neonatal hemochromatosis (disorder) Occurrence Perinatal state false Inferred relationship Existential restriction modifier (core metadata concept)
Neonatal hemochromatosis (disorder) Occurrence période périnatale false Inferred relationship Existential restriction modifier (core metadata concept)
Neonatal hemochromatosis (disorder) Is a Hemochromatosis (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Neonatal hemochromatosis (disorder) Finding site Digestive system subdivision false Inferred relationship Existential restriction modifier (core metadata concept)
Neonatal hemochromatosis (disorder) Associated morphology inflammation false Inferred relationship Existential restriction modifier (core metadata concept) 1
Neonatal hemochromatosis (disorder) Is a Neonatal disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Neonatal hemochromatosis (disorder) Occurrence Neonatal true Inferred relationship Existential restriction modifier (core metadata concept) 2
Neonatal hemochromatosis (disorder) Causative agent (attribute) Iron AND/OR iron compound false Inferred relationship Existential restriction modifier (core metadata concept)
Neonatal hemochromatosis (disorder) Is a Neonatal metabolic disorder (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Neonatal hemochromatosis (disorder) Causative agent (attribute) Iron and/or iron compound (substance) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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