About: Lecithin Acyltransferase Deficiency

Facets (new session)
Description
Metadata
Settings
- owl:sameAs
- Inference Rule:

About: Lecithin Acyltransferase Deficiency Goto Sponge Distinct Permalink

An Entity of Type : owl:Class, within Data Space : linked.opendata.cz associated with source document(s)

Attributes	Values
rdf:type	Class
rdfs:label	Lecithin Acyltransferase Deficiency
rdfs:subClassOf	Metabolism, Inborn Errors Rare Non-Neoplastic Disorder
Semantic_Type	Disease or Syndrome
Preferred_Name	Lecithin Acyltransferase Deficiency
UMLS_CUI	C0023195
FULL_SYN	Lecithin Acyltransferase DeficiencyPTNCI
DEFINITION	A disorder of lipoprotein metabolism caused by mutations in the LCAT gene. It is characterized by deficiency of the enzyme lecithin cholesterol acyltransferase. It is manifested with corneal opacity, hemolytic anemia, and proteinuria.NCI
code	C84813
http://linked.open...y/mesh/hasConcept	http://linked.opendata.cz/resource/mesh/concept/M0012277
is sameAs of	Lecithin Acyltransferase Deficiency

Faceted Search & Find service v1.16.118 as of Jun 21 2024

Alternative Linked Data Documents: ODE Content Formats:

RDF

ODATA

Microdata

About

OpenLink Virtuoso version 07.20.3240 as of Jun 21 2024, on Linux (x86_64-pc-linux-gnu), Single-Server Edition (126 GB total memory, 112 GB memory in use)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2024 OpenLink Software