loading...| Preferred Name | sickle cell anemia | |
| Synonyms |
Hemoglobin S disease restriction fragment length polymorphism, sickle cell Anemia-related HbS disease Haemoglobin S disease HPA 1 recognition polymorphism, beta-globin-related HPA1 Hb-SS disease without crisis Hb SC disease sickling disorder due to Haemoglobin S drepanocytosis Haemoglobin S disease without crisis sickle-cell/Hb-C disease without crisis hemoglobin SC disease sickle cell anemia Hemoglobin S disease without crisis sickling disorder due to Hemoglobin S Hb-S/Hb-C disease sickle cell disease haemoglobin SC disease Sickle Cell Disease |
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| Definitions |
Sickle cell anemias are chronic hemolytic diseases that may induce three types of acute accidents: severe anemia, severe bacterial infections, and ischemic vasoocclusive accidents (VOA) caused by sickle-shaped red blood cells obstructing small blood vessels and capillaries. Many diverse complications can occur. |
|
| ID |
http://purl.obolibrary.org/obo/MONDO_0011382 |
|
| database_cross_reference |
Orphanet:232 MESH:D000755 NANDO:2200624 DOID:0081445 UMLS:C0002895 ICD9:282.63 ICD9:282.60 OMIM:603903 NCIT:C34383 MedDRA:10040641 DOID:10923 GARD:8614 ICD9:282.6 MEDGEN:287 NORD:1714 |
|
| definition |
Sickle cell anemias are chronic hemolytic diseases that may induce three types of acute accidents: severe anemia, severe bacterial infections, and ischemic vasoocclusive accidents (VOA) caused by sickle-shaped red blood cells obstructing small blood vessels and capillaries. Many diverse complications can occur. |
|
| has_exact_synonym |
Hb-SS disease without crisis Hb SC disease sickling disorder due to Haemoglobin S drepanocytosis Haemoglobin S disease without crisis sickle-cell/Hb-C disease without crisis hemoglobin SC disease sickle cell anemia Hemoglobin S disease without crisis sickling disorder due to Hemoglobin S Hb-S/Hb-C disease sickle cell disease haemoglobin SC disease Sickle Cell Disease |
|
| has_related_synonym |
Hemoglobin S disease restriction fragment length polymorphism, sickle cell Anemia-related HbS disease Haemoglobin S disease HPA 1 recognition polymorphism, beta-globin-related HPA1 |
|
| IAO_0000233 | ||
| id |
MONDO:0011382 |
|
| in_subset |
http://purl.obolibrary.org/obo/mondo/mondo-base#rare http://purl.obolibrary.org/obo/mondo/mondo-base#otar http://purl.obolibrary.org/obo/mondo/mondo-base#gard_rare http://purl.obolibrary.org/obo/mondo/mondo-base#orphanet_rare http://purl.obolibrary.org/obo/mondo/mondo-base#nord_rare http://purl.obolibrary.org/obo/mondo/mondo-base#ordo_disorder |
|
| label |
sickle cell anemia |
|
| notation |
MONDO:0011382 |
|
| preferred label |
sickle cell anemia |
|
| prefLabel |
sickle cell anemia |
|
| skos_closeMatch | ||
| skos_exactMatch |
http://linkedlifedata.com/resource/umls/id/C0002895 http://purl.obolibrary.org/obo/NCIT_C34383 http://identifiers.org/mesh/D000755 http://identifiers.org/medgen/287 http://purl.obolibrary.org/obo/Orphanet_232 |
|
| subClassOf | ||
| excluded_subClassOf |
http://purl.obolibrary.org/obo/MONDO_0018384 |