| immunodeficiëntie door verstoorde expressie van humaan leukocytenantigeen klasse 1 door mutatie van 'transporter 2, ATP binding cassette subfamily B member' (aandoening) | | immunodeficiëntie door verstoorde expressie van humaan leukocytenantigeen klasse 1 door mutatie van TAP2 | | deficiëntie van HLA1 door mutatie van TAP2
immunodeficiëntie door verstoorde expressie van humaan leukocytenantigeen klasse 1 door mutatie van 'transporter 2, ATP binding cassette subfamily B member'
immunodeficiëntie door defect in expressie van MHC-I door mutatie van TAP2
| | Major histocompatibility complex class I deficiency due to TAP2 mutation | | MHC (major histocompatibility complex) class I deficiency due to TAP2 mutation
Immunodeficiency by defective expression of major histocompatibility complex class I due to transporter 2, ATP binding cassette subfamily B member mutation
Immunodeficiency by defective expression of human leukocyte antigen class 1 due to transporter 2, ATP binding cassette subfamily B member mutation
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| | Id | 1351355003 | | Status | Primitive |
| SNOMED CT to ICD-10 extended map | | Target | D81.6 | | Rule | TRUE | | Advice | ALWAYS D81.6 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION | | Correlation | SNOMED CT source code to target map code correlation not specified |
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