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57835009: Hepatic methionine adenosyltransferase deficiency (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
96167011 Hepatic methionine adenosyltransferase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
96168018 MAT deficiency en Synonym Active Entire term case sensitive SNOMED CT core module
198791018 Methionine adenosyltransferase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
796501013 Hepatic methionine adenosyltransferase deficiency (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hepatic methionine adenosyltransferase deficiency Is a Digestive system hereditary disorder false Inferred relationship Existential restriction modifier
Hepatic methionine adenosyltransferase deficiency Is a Enzymopathy true Inferred relationship Existential restriction modifier
Hepatic methionine adenosyltransferase deficiency Is a Congenital anomaly of liver false Inferred relationship Existential restriction modifier
Hepatic methionine adenosyltransferase deficiency Is a Hypermethioninemia true Inferred relationship Existential restriction modifier
Hepatic methionine adenosyltransferase deficiency Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Hepatic methionine adenosyltransferase deficiency Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 1
Hepatic methionine adenosyltransferase deficiency Finding site Liver structure false Inferred relationship Existential restriction modifier 1
Hepatic methionine adenosyltransferase deficiency Finding site Digestive organ structure false Inferred relationship Existential restriction modifier 1
Hepatic methionine adenosyltransferase deficiency Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Hepatic methionine adenosyltransferase deficiency Finding site Structure of digestive system false Inferred relationship Existential restriction modifier 1
Hepatic methionine adenosyltransferase deficiency Is a Congenital anomaly of trunk false Inferred relationship Existential restriction modifier
Hepatic methionine adenosyltransferase deficiency Is a Inborn error of metabolism true Inferred relationship Existential restriction modifier
Hepatic methionine adenosyltransferase deficiency Is a Congenital anomaly of abdomen false Inferred relationship Existential restriction modifier
Hepatic methionine adenosyltransferase deficiency Is a Congenital anomaly of body cavity false Inferred relationship Existential restriction modifier
Hepatic methionine adenosyltransferase deficiency Finding site Liver structure false Inferred relationship Existential restriction modifier 1
Hepatic methionine adenosyltransferase deficiency Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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