loading...| Preferred Name | familial hemolytic anemia | |
| Synonyms |
anemia hemolytic congenital anaemia hemolytic congenital hereditary hemolytic anaemia hereditary hemolytic anemia congenital hemolytic anemia congenital hemolytic anaemia |
|
| Definitions |
A congenital hemolytic anemia caused by defects of the erythrocyte membrane, enzyme deficiencies, or hemoglobinopathies. |
|
| ID |
http://purl.obolibrary.org/obo/MONDO_0003689 |
|
| database_cross_reference |
SCTID:42601008 UMLS:C0002881 NCIT:C34379 MESH:D000745 NANDO:2100183 MEDGEN:1919 DOID:589 GARD:6167 ICD9:282 ICD9:282.9 |
|
| definition |
A congenital hemolytic anemia caused by defects of the erythrocyte membrane, enzyme deficiencies, or hemoglobinopathies. |
|
| has_exact_synonym |
hereditary hemolytic anaemia hereditary hemolytic anemia congenital hemolytic anemia congenital hemolytic anaemia |
|
| has_related_synonym |
anemia hemolytic congenital anaemia hemolytic congenital |
|
| id |
MONDO:0003689 |
|
| in_subset |
http://purl.obolibrary.org/obo/mondo/mondo-base#rare |
|
| label |
familial hemolytic anemia |
|
| notation |
MONDO:0003689 |
|
| preferred label |
familial hemolytic anemia |
|
| prefLabel |
familial hemolytic anemia |
|
| see also |
https://rarediseases.info.nih.gov/diseases/6167/congenital-hemolytic-anemia |
|
| skos_exactMatch |
http://purl.obolibrary.org/obo/NCIT_C34379 http://identifiers.org/mesh/D000745 http://purl.obolibrary.org/obo/DOID_589 http://identifiers.org/snomedct/42601008 |
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| subClassOf |