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loading...| Preferred Name |
Hemoglobin_Bart_s_Hydrops_Syndrome |
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| Synonyms |
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| ID |
http://www.owl-ontologies.com/Ontology1358660052.owl#Hemoglobin_Bart_s_Hydrops_Syndrome |
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| ID |
C84767 |
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| NCI_Definition |
A condition characterized by fluid accumulation in two or more anatomic compartments in the fetus. Causes include Rh incompatibility, congenital heart defects, and chromosomal abnormalities. |
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| NCI_PT |
Hydrops Fetalis |
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| NICHD_Definition |
_ |
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| prefixIRI |
Hemoglobin_Bart_s_Hydrops_Syndrome |
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| prefLabel |
Hemoglobin_Bart_s_Hydrops_Syndrome |
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| Subset_Association1 |
NICHD Pediatric Terminology |
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| Subset_Association2 |
Neonatal Research Network Terminology |
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| SYN |
Hydrops Fetalis |
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| subClassOf |
http://www.owl-ontologies.com/Ontology1358660052.owl#Fetal_Disorder |
Create mapping
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| http://purl.bioontology.org/ontology/SNMI/DC-13850 | SNMI | LOOM | |
| http://purl.bioontology.org/ontology/SNOMEDCT/5300004 | SNOMEDCT | LOOM |