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93369005: Congenital microhepatia (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Viscus structure finding (finding)\Abdominal organ finding\Liver finding\Disease of liver\Congenital anomaly of liver\Congenital microhepatia

\Digestive system finding (finding)\Liver finding\Disease of liver\Congenital anomaly of liver\Congenital microhepatia
\Digestive system finding (finding)\Disease of digestive system (disorder)\Disorder of digestive organ\Disorder of liver and/or biliary tract\Congenital abnormality of liver and biliary tract (disorder)\Congenital anomaly of liver\Congenital microhepatia
\Digestive system finding (finding)\Disease of digestive system (disorder)\Disorder of digestive organ\Disorder of liver and/or biliary tract\Disease of liver\Congenital anomaly of liver\Congenital microhepatia
\Digestive system finding (finding)\Disease of digestive system (disorder)\Disorder of digestive organ\Congenital anomaly of digestive organ (disorder)\Congenital abnormality of liver and biliary tract (disorder)\Congenital anomaly of liver\Congenital microhepatia
\Digestive system finding (finding)\Disease of digestive system (disorder)\Disorder of digestive system specific to fetus OR newborn\Congenital anomaly of digestive system\Congenital anomaly of digestive organ (disorder)\Congenital abnormality of liver and biliary tract (disorder)\Congenital anomaly of liver\Congenital microhepatia

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Congenital microhepatia	Is a	Congenital anomaly of liver	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital microhepatia	Associated morphology	anomalie du développement	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital microhepatia	Finding site	Liver structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital microhepatia	Associated morphology	Congenital smallness	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital microhepatia	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital microhepatia	Finding site	Digestive organ structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital microhepatia	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital microhepatia	Is a	Congenital anomaly of abdomen	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital microhepatia	Is a	Congenital anomaly of body cavity	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital microhepatia	Finding site	Liver structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital microhepatia	Associated morphology	Congenital smallness	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Congenital microhepatia	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Congenital microhepatia	Associated morphology	anomalie du développement	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital microhepatia	Finding site	Liver structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital microhepatia	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital microhepatia	Associated morphology	Congenital smallness	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital microhepatia	Finding site	Entire liver	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital microhepatia	Finding site	Entire liver	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Congenital microhepatia	Pathological process (attribute)	Pathological developmental process (qualifier value)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital microhepatia	Associated morphology	Abnormal smallness (morphologic abnormality)	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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Id	Description	Lang	Type	Status	Case?	Module
154534011	Congenital microhepatia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
154535012	Congenital small liver	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
837087011	Congenital microhepatia (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
154534011	Congenital microhepatia	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
154534011	Congenital microhepatia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
154535012	Congenital small liver	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
154535012	Congenital small liver	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
837087011	Congenital microhepatia (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
837087011	Congenital microhepatia (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4710651000241118	hypoplasie congénitale du foie	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
4710651000241118	hypoplasie congénitale du foie	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module