About: Hereditary pyropoikilocytosis

Facets (new session)
Description
Metadata
Settings
- Rule:
- Inverse Functional Properties:
- "Same As":

About: Hereditary pyropoikilocytosis Goto Sponge NotDistinct Permalink

An Entity of Type : yago:WikicatRedBloodCellDisorders, within Data Space : dbpedia.demo.openlinksw.com associated with source document(s)
QRcode icon

http://dbpedia.demo.openlinksw.com/describe/?url=http%3A%2F%2Fdbpedia.org%2Fresource%2FHereditary_pyropoikilocytosis&invfp=IFP_OFF&sas=SAME_AS_OFF

Hereditary pyropoikilocytosis (HPP) is an autosomal recessive form of hemolytic anemia characterized by an abnormal sensitivity of red blood cells to heat and erythrocyte morphology similar to that seen in thermal burns or from prolonged exposure of a healthy patient's blood sample to high ambient temperatures. Patients with HPP tend to experience severe hemolysis and anemia in infancy that gradually improves, evolving toward typical elliptocytosis later in life. However, the hemolysis can lead to rapid sequestration and destruction of red cells. Splenectomy is curative when this occurs.

Attributes	Values
rdf:type	Thing Disease yago:WikicatAutosomalRecessiveDisorders yago:WikicatCytoskeletalDefects yago:Abstraction100002137 yago:Attribute100024264 yago:Condition113920835 yago:Defect114464005 yago:Disease114070360 yago:Disorder114052403 yago:IllHealth114052046 yago:Illness114061805 yago:Imperfection114462666 yago:PathologicalState114051917 yago:PhysicalCondition114034177 disease yago:State100024720 yago:WikicatRedBloodCellDisorders
rdfs:label	Hereditary pyropoikilocytosis (en)
rdfs:comment	Hereditary pyropoikilocytosis (HPP) is an autosomal recessive form of hemolytic anemia characterized by an abnormal sensitivity of red blood cells to heat and erythrocyte morphology similar to that seen in thermal burns or from prolonged exposure of a healthy patient's blood sample to high ambient temperatures. Patients with HPP tend to experience severe hemolysis and anemia in infancy that gradually improves, evolving toward typical elliptocytosis later in life. However, the hemolysis can lead to rapid sequestration and destruction of red cells. Splenectomy is curative when this occurs. (en)
foaf:name	Hereditary pyropoikilocytosis (en)
name	Hereditary pyropoikilocytosis (en)
foaf:depiction
dcterms:subject	Cytoskeletal defects Autosomal recessive disorders Red blood cell disorders
Wikipage page ID	3725759 (xsd:integer)
Wikipage revision ID	1043700757 (xsd:integer)
Link from a Wikipage to another Wikipage	List of hematologic conditions Cytoskeletal defects Autosomal recessive disorders Anemia Hemolysis Hemolytic anemia Poikilocytosis Autosomal recessive Red blood cell disorders Red blood cell Hereditary elliptocytosis Splenectomy Spectrin Elliptocytosis Erythrocyte dbr:Spectrin_deficiency
sameAs	Hereditary pyropoikilocytosis Hereditary pyropoikilocytosis Hereditary pyropoikilocytosis Hereditary pyropoikilocytosis
dbp:wikiPageUsesTemplate	dbt:Genetic-disorder-stub dbt:Cytoskeletal_defects dbt:Citation_needed dbt:Infobox_medical_condition_(new) dbt:Medical_resources dbt:Reflist dbt:Medicine dbt:Blood-disease-stub
thumbnail	wiki-commons:Special:FilePath/Autosomal_recessive_-_en.svg?width=300
OMIM	266140 (xsd:integer)
caption	Hereditary pyropoikilocytosis is autosomal recessive (en)
field	hematology (en)
synonyms	Pyropoikilocytosis hereditary (en)
has abstract	Hereditary pyropoikilocytosis (HPP) is an autosomal recessive form of hemolytic anemia characterized by an abnormal sensitivity of red blood cells to heat and erythrocyte morphology similar to that seen in thermal burns or from prolonged exposure of a healthy patient's blood sample to high ambient temperatures. Patients with HPP tend to experience severe hemolysis and anemia in infancy that gradually improves, evolving toward typical elliptocytosis later in life. However, the hemolysis can lead to rapid sequestration and destruction of red cells. Splenectomy is curative when this occurs. HPP has been associated with a defect of the erythrocyte membrane protein spectrin and with . It was characterized in 1975. It is considered a severe form of hereditary elliptocytosis. (en)
gold:hypernym	Form
prov:wasDerivedFrom	wikipedia-en:Hereditary_pyropoikilocytosis?oldid=1043700757&ns=0
page length (characters) of wiki page	4178 (xsd:nonNegativeInteger)
OMIM id	266140 (xsd:integer)
foaf:isPrimaryTopicOf	wikipedia-en:Hereditary_pyropoikilocytosis
is Link from a Wikipage to another Wikipage of	Dyserythropoiesis List of hematologic conditions HPP Hereditary elliptocytosis Aldolase A deficiency Pyropoikilocytosis
is Wikipage redirect of	Pyropoikilocytosis
is foaf:primaryTopic of	wikipedia-en:Hereditary_pyropoikilocytosis

Faceted Search & Find service v1.17_git139 as of Feb 29 2024

Alternative Linked Data Documents: ODE Content Formats:

RDF

ODATA

Microdata

About

OpenLink Virtuoso version 08.03.3330 as of Mar 19 2024, on Linux (x86_64-generic-linux-glibc212), Single-Server Edition (378 GB total memory, 53 GB memory in use)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2024 OpenLink Software