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loading...| Preferred Name |
Hemoglobin Trait |
|
| Synonyms |
Hemoglobin Trait |
|
| Definitions |
A condition in which a person is heterozygous for a globin gene, with a one normal allele and one defective allele. |
|
| ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C95534 |
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| ALT_DEFINITION |
A condition in which a person has a combination of normal and abnormal globin alleles with minimal or no clinical phenotype. |
|
| code |
C95534 |
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| Concept_In_Subset | ||
| Contributing_Source |
NICHD |
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| DEFINITION |
A condition in which a person is heterozygous for a globin gene, with a one normal allele and one defective allele. |
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| FULL_SYN |
Hemoglobin Trait |
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| label |
Hemoglobin Trait |
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| Preferred_Name |
Hemoglobin Trait |
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| prefixIRI |
Thesaurus:C95534 |
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| Semantic_Type |
Disease or Syndrome |
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| UMLS_CUI |
C2987213 |
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| subClassOf |
Create mapping
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| http://purl.obolibrary.org/obo/NCIT_C95534 | BERO | LOOM | |
| http://purl.obolibrary.org/obo/NCIT_C95534 | SCDO | LOOM | |
| http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#Hemoglobin_Trait | CSEO | LOOM |