loading...| Preferred Name |
alpha thalassemia |
|
| Synonyms |
alpha-thalassemia Alpha thalassaemia A-thalassemia |
|
| Definitions |
Alpha-thalassemia is an inherited hemoglobinopathy characterized by impaired synthesis of alpha-globin chains leading to a variable clinical picture depending on the number of affected alleles. |
|
| ID |
http://purl.obolibrary.org/obo/MONDO_0011399 |
|
| closeMatch | ||
| database_cross_reference |
GARD:0000621 NCIT:C34368 MedDRA:10043390 UMLS:C0002312 OMIM:604131 ICD9:282.43 ICD10:D56.0 Orphanet:846 MESH:D017085 ICD9:282.49 COHD:4287844 SCTID:68913001 DOID:1099 |
|
| exactMatch |
http://purl.obolibrary.org/obo/NCIT_C34368 http://linkedlifedata.com/resource/umls/id/C0002312 http://purl.obolibrary.org/obo/DOID_1099 http://identifiers.org/meddra/10043390 http://www.orpha.net/ORDO/Orphanet_846 http://identifiers.org/omim/604131 http://identifiers.org/mesh/D017085 |
|
| has exact synonym |
alpha-thalassemia Alpha thalassaemia |
|
| has related synonym |
A-thalassemia |
|
| id |
MONDO:0011399 |
|
| imported from | ||
| in_subset | ||
| label |
alpha thalassemia |
|
| notation |
MONDO:0011399 |
|
| prefLabel |
alpha thalassemia |
|
| textual definition |
Alpha-thalassemia is an inherited hemoglobinopathy characterized by impaired synthesis of alpha-globin chains leading to a variable clinical picture depending on the number of affected alleles. |
|
| subClassOf |
http://purl.obolibrary.org/obo/MONDO_0019747 |