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238091006: Lecithin cholesterol acyltransferase 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
356906011 Lecithin cholesterol acyltransferase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
626925017 Lecithin cholesterol acyltransferase deficiency (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

1 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Lecithin cholesterol acyltransferase deficiency Is a Congenital anomaly of the hematopoietic system false Inferred relationship Existential restriction modifier
Lecithin cholesterol acyltransferase deficiency Is a Erythrocyte membrane abnormality true Inferred relationship Existential restriction modifier
Lecithin cholesterol acyltransferase deficiency Is a Hereditary disorder of hematologic system false Inferred relationship Existential restriction modifier
Lecithin cholesterol acyltransferase deficiency Is a Hypoalphalipoproteinemia true Inferred relationship Existential restriction modifier
Lecithin cholesterol acyltransferase deficiency Occurrence Congenital false Inferred relationship Existential restriction modifier
Lecithin cholesterol acyltransferase deficiency Finding site Erythrocyte true Inferred relationship Existential restriction modifier 1
Lecithin cholesterol acyltransferase deficiency Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier
Lecithin cholesterol acyltransferase deficiency Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier
Lecithin cholesterol acyltransferase deficiency Has definitional manifestation Red blood cell finding false Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
Fish-eye disease Is a True Lecithin cholesterol acyltransferase deficiency Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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