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79607001: Congenital hepatic fibrosis (disorder)

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

\Viscus structure finding (finding)\Abdominal organ finding\Liver finding\Disease of liver\...

\Lesion of liver (disorder)\Hepatic fibrosis\Congenital hepatic fibrosis

\Congenital anomaly of liver\Congenital hepatic fibrosis

\Digestive system finding (finding)\Liver finding\Disease of liver\Lesion of liver (disorder)\Hepatic fibrosis\Congenital hepatic fibrosis
\Digestive system finding (finding)\Liver finding\Disease of liver\Congenital anomaly of liver\Congenital hepatic fibrosis
\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 hepatic fibrosis
\Digestive system finding (finding)\Disease of digestive system (disorder)\Disorder of digestive organ\Disorder of liver and/or biliary tract\Disease of liver\Lesion of liver (disorder)\Hepatic fibrosis\Congenital hepatic fibrosis
\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 hepatic fibrosis
\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 hepatic fibrosis
\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 hepatic fibrosis

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 hepatic fibrosis	Is a	Congenital anomaly of liver	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital hepatic fibrosis	Is a	Perinatal disorders of liver and/or biliary system	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital hepatic fibrosis	Is a	Hepatic fibrosis	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital hepatic fibrosis	Associated morphology	Fibrosis (morphologic abnormality)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital hepatic fibrosis	Finding site	Liver structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital hepatic fibrosis	Associated morphology	anomalie du développement	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital hepatic fibrosis	Associated morphology	Nodular regeneration	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital hepatic fibrosis	Finding site	Digestive system subdivision	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital hepatic fibrosis	Occurrence	Perinatal state	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital hepatic fibrosis	Finding site	Liver structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Congenital hepatic fibrosis	Associated morphology	Fibrosis (morphologic abnormality)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Congenital hepatic fibrosis	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital hepatic fibrosis	Finding site	Liver structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital hepatic fibrosis	Associated morphology	anomalie congénitale	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital hepatic fibrosis	Occurrence	période périnatale	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital hepatic fibrosis	Finding site	Digestive organ structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital hepatic fibrosis	Finding site	Liver structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital hepatic fibrosis	Finding site	Liver structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Congenital hepatic fibrosis	Finding site	Liver structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Congenital hepatic fibrosis	Finding site	Liver structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Congenital hepatic fibrosis	Finding site	Digestive system subdivision	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital hepatic fibrosis	Finding site	Liver structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital hepatic fibrosis	Finding site	Liver structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Congenital hepatic fibrosis	Finding site	Liver structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital hepatic fibrosis	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital hepatic fibrosis	Finding site	Liver structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital hepatic fibrosis	Finding site	Liver structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital hepatic fibrosis	Finding site	Liver structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital hepatic fibrosis	Finding site	Liver structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital hepatic fibrosis	Finding site	Liver structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital hepatic fibrosis	Finding site	Liver structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital hepatic fibrosis	Finding site	Liver structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital hepatic fibrosis	Finding site	Liver structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital hepatic fibrosis	Finding site	Liver structure (body structure)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital hepatic fibrosis	Finding site	Liver structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital hepatic fibrosis	Is a	Congenital anomaly of abdomen	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital hepatic fibrosis	Is a	Congenital anomaly of body cavity	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital hepatic fibrosis	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Congenital hepatic fibrosis	Associated morphology	anomalie du développement	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Congenital hepatic fibrosis	Finding site	Liver structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Congenital hepatic fibrosis	Is a	Congenital disease	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital hepatic fibrosis	Associated morphology	Fibrosis (morphologic abnormality)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital hepatic fibrosis	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital hepatic fibrosis	Pathological process (attribute)	Pathological developmental process (qualifier value)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital hepatic fibrosis	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Boichis syndrome	Is a	True	Congenital hepatic fibrosis	Inferred relationship	Existential restriction modifier (core metadata concept)
Joubert syndrome with congenital hepatic fibrosis (disorder)	Is a	True	Congenital hepatic fibrosis	Inferred relationship	Existential restriction modifier (core metadata concept)
A rare syndromic intellectual disability characterised by early developmental delay with failure to thrive, intellectual disability, congenital hepatic fibrosis, renal cystic dysplasia, and dysmorphic facial features (bilateral ptosis, anteverted nostrils, high arched palate, and micrognathia). Variable additional features have been reported, including cerebellar anomalies, postaxial polydactyly, syndactyly, genital anomalies, tachypnoea. There have been no further descriptions in the literature since 1987.	Is a	True	Congenital hepatic fibrosis	Inferred relationship	Existential restriction modifier (core metadata concept)
Nephrocystin 3-related Meckel-like syndrome (disorder)	Is a	True	Congenital hepatic fibrosis	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital cystic disease of liver	Is a	True	Congenital hepatic fibrosis	Inferred relationship	Existential restriction modifier (core metadata concept)
Caroli syndrome (disorder)	Is a	True	Congenital hepatic fibrosis	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
132070012	Congenital hepatic fibrosis	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
820676011	Congenital hepatic fibrosis (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
132070012	Congenital hepatic fibrosis	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
132070012	Congenital hepatic fibrosis	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
820676011	Congenital hepatic fibrosis (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
820676011	Congenital hepatic fibrosis (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3421221001000111	Leberfibrose, isolierte, kongenitale	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
4650351000241112	fibrose hépatique congénitale	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
4650351000241112	fibrose hépatique congénitale	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3421221001000111	Leberfibrose, isolierte, kongenitale	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module