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Cell Culture Ontology
Last uploaded:
July 23, 2014
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Preferred Name | obsolete_Fanconi anemia | |
Synonyms |
Fanconi pancytopenia |
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Definitions |
Fanconi anemia (FA) is a hereditary DNA repair disorder characterized by progressive pancytopenia with bone marrow failure, variable congenital malformations and predisposition to develop hematological or solid tumors. |
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ID |
http://www.orpha.net/ORDO/Orphanet_84 |
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Obsolete |
true |
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database_cross_reference |
ICD10:D61.0 OMIM:227650 OMIM:613390 OMIM:300514 OMIM:610832 OMIM:614082 OMIM:614087 OMIM:614083 UMLS:C0015625 MeSH:D005199 OMIM:615272 OMIM:227645 OMIM:227646 OMIM:600901 OMIM:613951 OMIM:603467 OMIM:609054 OMIM:609053 OMIM:616435 OMIM:617243 OMIM:617244 OMIM:617247 MedDRA:10055206
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definition |
Fanconi anemia (FA) is a hereditary DNA repair disorder characterized by progressive pancytopenia with bone marrow failure, variable congenital malformations and predisposition to develop hematological or solid tumors.
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definition_citation |
orphanet
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deprecated |
true
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has_exact_synonym |
Fanconi pancytopenia
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label |
obsolete_Fanconi anemia
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obsoleted_in_version |
3.41.0
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preferred label |
obsolete_Fanconi anemia
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prefLabel |
obsolete_Fanconi anemia
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reason_for_obsolescence |
Replaced with Mondo term.
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term replaced by | ||
subClassOf |
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Delete | Subject | Author | Type | Created |
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Mapping To | Ontology | Source |
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http://www.orpha.net/ORDO/Orphanet_84 | EFO | SAME_URI |
http://www.orpha.net/ORDO/Orphanet_84 | ORDO | SAME_URI |
http://www.orpha.net/ORDO/Orphanet_84 | EFO | LOOM |