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