Preferred Name | Hemoglobinopathies | |
Synonyms |
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|
ID |
http://www.phoc.org.cn/pmo/class/PMO_00036627 |
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Database_Cross_Reference |
MDR:10018902 RCDAE:X20Ci SNOMEDCT_US:80141007 MDR:10060892 NDFRT:N0000001472 SNOMEDCT_US:267556002 NCI:C3092 SNOMEDCT_US:154794008 SNM:D-4130 SNMI:DC-20000 COSTAR:NOCODE CSP:1418-5657 CHV:0000005994 AOD:0000005748 LCH:U002149 LNC:LP31618-9 CST:HEMRBCDIS NCI_NICHD:C3092 LCH_NW:sh85060203 MDR:10018905 ICD10CM:D58.2 MTH:U000166 MDR:10018903 RCD:X20Ci MSH:D006453 LNC:MTHU029621 LNC:LA16207-5 CST:HAL/RBC/HGB MEDCIN:277675 MDR:10055610 DO:DOID:2860 CCPSS:1017538 BI:BI00313 MTHICD9:282.7 |
|
label |
Hemoglobinopathies |
|
MCID |
MC00006075 |
|
PMOID |
PMO:00036627 |
|
prefixIRI |
pmo:PMO_00036627 |
|
prefLabel |
Hemoglobinopathies |
|
Synonym |
Hemoglobinopathy NOS HEMOGLOBINOPATHY haemoglobinopathy Hemoglobinopathy, NOS diseases hemoglobin hemoglobinopathy Haemoglobin disease Hemoglobinopathies [Disease/Finding] HEMOGLOBIN DISORDER Haemoglobin disorder hemoglobin disorders Hemoglobinopathy Hemoglobin disorder Hemoglobin disorders hemoglobinopathies Haemoglobinopathies Hemoglobin disease disorders hemoglobin Hemoglobin disorder, NOS Haemoglobin disease, NOS Haemoglobinopathy, NOS Globin abnormality C-20 HEMOGLOBINOPATHIES Hemoglobin disease, NOS Haemoglobinopathy Haemoglobinopathy NOS hemoglobinopathy (diagnosis) haemoglobinopathies Haemoglobinopathies congenital hemoglobin disease haemoglobin disease Hemoglobinopathies congenital HEMOGLOBINOPATHIES Globin abnormality, NOS Hemoglobinopathy (disorder) Haemoglobin disorder, NOS hemoglobin disorder Hemoglobinopathies / Iron Metabolism |
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Tree Number |
T9.8.4.25 T9.5.2.2 |
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subClassOf |