Preferred Name

Hemoglobinopathies [Disease/Finding]

Synonyms
ID

http://evs.nci.nih.gov/ftp1/NDF-RT/NDF-RT.owl#N0000001472

code

C3122

Display_Name

Hemoglobinopathies

imported from

http://evs.nci.nih.gov/ftp1/NDF-RT/NDF-RT.owl

label

Hemoglobinopathies [Disease/Finding]

MeSH_CUI

M0010129

MeSH_Definition

A group of inherited disorders characterized by structural alterations within the hemoglobin molecule.

MeSH_DUI

D006453

MeSH_Name

Hemoglobinopathies

NUI

N0000001472

prefixIRI

NDF-RT:N0000001472

prefLabel

Hemoglobinopathies [Disease/Finding]

RxNorm_CUI

1023547

SNOMED_CID

80141007

UMLS_CUI

C0019045

subClassOf

http://evs.nci.nih.gov/ftp1/NDF-RT/NDF-RT.owl#N0000001459

http://evs.nci.nih.gov/ftp1/NDF-RT/NDF-RT.owl#N0000011105

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