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deficiëntie van alfa-N-acetylgalactosaminidase type 1 (aandoening)
deficiëntie van alfa-N-acetylgalactosaminidase type 1
ziekte van Schindler type 1
alfa-N-acetylgalactosaminidasedeficiëntie type 1
NAGA-deficiëntie type 1
Alpha-N-acetylgalactosaminidase deficiency type 1
NAGA - Alpha-N-acetylgalactosaminidase deficiency type 1
Schindler disease type 1
A very rare and severe type of NAGA deficiency characterized by infantile neuroaxonal dystrophy.
Id879937000
StatusPrimitive
Occurrencecongenitaal
referentieset met complexe 'mapping' naar ICD-10
TargetE77.1
RuleTRUE
AdviceALWAYS E77.1 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified