About: Alpha Thalassemia     Goto   Sponge   NotDistinct   Permalink

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

AttributesValues
rdf:type
rdfs:label
  • Alpha Thalassemia
rdfs:subClassOf
Semantic_Type
  • Disease or Syndrome
Preferred_Name
  • Alpha Thalassemia
UMLS_CUI
  • C0002312
ALT_DEFINITION
  • A disorder characterized by reduced synthesis of the alpha chains of hemoglobin. The severity of this condition can vary from mild anemia to death, depending on the number of genes deleted.MSH2003_2003_05_12
Legacy_Concept_Name
  • Alpha_Thalassemia
FULL_SYN
  • Alpha ThalassemiaPTNCI
DEFINITION
  • A genetic hematologic disorder characterized by partial or complete absence of the alpha globin chains of the heme molecule.NCI
code
  • C34368
http://linked.open...y/mesh/hasConcept
is rdfs:subClassOf of
is someValuesFrom of
is sameAs of
Faceted Search & Find service v1.16.118 as of Jun 21 2024


Alternative Linked Data Documents: ODE     Content Formats:   [cxml] [csv]     RDF   [text] [turtle] [ld+json] [rdf+json] [rdf+xml]     ODATA   [atom+xml] [odata+json]     Microdata   [microdata+json] [html]    About   
This material is Open Knowledge   W3C Semantic Web Technology [RDF Data] Valid XHTML + RDFa
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, 32 GB memory in use)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2024 OpenLink Software