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Ovalocytosis, Hereditary Hemolytic, with Defective Erythropoiesis
MeSH Supplementary Concept Data 2023
Details
Concepts
MeSH Supplementary
Ovalocytosis, Hereditary Hemolytic, with Defective Erythropoiesis
Unique ID
C563479
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C563479
Registry Number
0
Heading Mapped to
*Elliptocytosis, Hereditary
Frequency
0
Date of Entry
2012/11/05
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Ovalocytosis, Hereditary Hemolytic, with Defective Erythropoiesis
Preferred
Concept UI
M0563779
Registry Number
0
Terms
Ovalocytosis, Hereditary Hemolytic, with Defective Erythropoiesis
Preferred Term
Term UI
T828393
Date
08/22/2012
LexicalTag
NON
ThesaurusID
OMIM (2013)
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