loading...| Preferred Name | Hereditary persistence of fetal hemoglobin | |
| Synonyms |
Hereditary persistence of fetal haemoglobin Hereditary persistence of foetal haemoglobin Hb F disease Hereditary persistence of fetal hemoglobin (disorder) HPFH - Hereditary persistence of fetal hemoglobin HPFH - Hereditary persistence of fetal haemoglobin HPFH - Hereditary persistence of foetal haemoglobin |
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| ID |
http://purl.bioontology.org/ontology/SNOMEDCT/191201002 |
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| Active |
1 |
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| altLabel |
Hereditary persistence of fetal haemoglobin Hereditary persistence of foetal haemoglobin Hb F disease Hereditary persistence of fetal hemoglobin (disorder) HPFH - Hereditary persistence of fetal hemoglobin HPFH - Hereditary persistence of fetal haemoglobin HPFH - Hereditary persistence of foetal haemoglobin |
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| CASE SIGNIFICANCE ID |
900000000000448009 900000000000017005 |
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| CTV3ID |
D1071 |
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| cui |
C0019025 |
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| DEFINITION STATUS ID |
900000000000074008 |
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| Effective time |
20020131 |
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| Has finding site | ||
| notation |
191201002 |
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| Occurs in | ||
| prefLabel |
Hereditary persistence of fetal hemoglobin |
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| Subset member |
447562003~MAPRULE~TRUE 6011000124106~MAPADVICE~MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA 6011000124106~MAPADVICE~ALWAYS D56.4 900000000000497000~MAPTARGET~D1071 6011000124106~MAPTARGET~ 6011000124106~MAPCATEGORYID~447638001 6011000124106~MAPGROUP~1 6011000124106~MAPGROUP~2 6011000124106~MAPTARGET~D56.4 900000000000508004~ACCEPTABILITYID~900000000000549004 447562003~MAPGROUP~1 447562003~CORRELATIONID~447561005 6011000124106~MAPCATEGORYID~447637006 900000000000509007~ACCEPTABILITYID~900000000000548007 6011000124106~MAPADVICE~IF HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN WITH SICKLE CELL DISEASE SYNDROME CHOOSE D56.4 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 900000000000508004~ACCEPTABILITYID~900000000000548007 6011000124106~MAPRULE~IFA 783254003 | Hereditary persistence of fetal hemoglobin with sickle cell disease syndrome | 6011000124106~MAPTARGET~D57.1 447562003~MAPPRIORITY~1 447562003~MAPCATEGORYID~447637006 6011000124106~MAPRULE~OTHERWISE TRUE 6011000124106~MAPCATEGORYID~447639009 447562003~MAPTARGET~D56.4 6011000124106~MAPPRIORITY~1 6011000124106~CORRELATIONID~447561005 447562003~MAPADVICE~ALWAYS D56.4 6011000124106~MAPADVICE~IF HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN WITH SICKLE CELL DISEASE SYNDROME CHOOSE D57.1 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPRULE~TRUE 900000000000509007~ACCEPTABILITYID~900000000000549004 6011000124106~MAPPRIORITY~2 |
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| tui |
T047 |
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| Type ID |
900000000000003001 900000000000013009 |
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| subClassOf |