| immunodeficiëntie door verstoorde expressie van humaan leukocytenantigeen klasse 1 door mutatie van 'transporter 1, ATP binding cassette subfamily B member' (aandoening) | | immunodeficiëntie door verstoorde expressie van humaan leukocytenantigeen klasse 1 door mutatie van TAP1 | | immunodeficiëntie door verstoorde expressie van humaan leukocytenantigeen klasse 1 door mutatie van 'transporter 1, ATP binding cassette subfamily B member'
deficiëntie van HLA1 door mutatie van TAP1
immunodeficiëntie door defect in expressie van MHC-I door mutatie van TAP1
| | Major histocompatibility complex class I deficiency due to TAP1 mutation | | Immunodeficiency by defective expression of major histocompatibility complex class I due to transporter 1, ATP binding cassette subfamily B member mutation
Immunodeficiency by defective expression of human leukocyte antigen class 1 due to transporter 1, ATP binding cassette subfamily B member mutation
MHC (major histocompatibility complex) class I deficiency due to TAP1 mutation
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| | Id | 1351354004 | | 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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