anhidrotische ectodermale dysplasie met immunodeficiëntie	autosomaal dominante hereditaire aandoening	hereditaire aandoening van gebitselement	hereditaire aandoening van immuunsysteem	hereditaire aandoening van integumentum	hereditaire ontwikkelingsstoornis
\|	\|	\|	\|	\|	\|

Anhidrotic ectodermal dysplasia with immune deficiency due to nuclear factor kappa-B inhibitor alpha, gain of function mutation (disorder)
	Anhidrotic ectodermal dysplasia with immune deficiency due to IKBA gain of function mutation
	Anhidrotic ectodermal dysplasia with immune deficiency due to IKBA GOF (gain of function) mutation Anhidrotic ectodermal dysplasia with immune deficiency due to NFKBIA gain of function mutation Anhidrotic ectodermal dysplasia with immune deficiency due to nuclear factor kappa-B inhibitor alpha, gain of function mutation

Id	1354646005
Status	Primitive

Pathological process

afwijkend immuunproces

Has interpretation	afwijkend
Interprets	zweten

Associated morphology	dysplasie
Finding site	structuur van ectoderm
Occurrence	congenitaal
Pathological process	proces van pathologische ontwikkeling

Associated morphology	morfologische afwijking
Finding site	structuur van gebitselement
Occurrence	congenitaal
Pathological process	proces van pathologische ontwikkeling

Associated morphology	morfologische afwijking
Finding site	structuur van pilus
Occurrence	congenitaal
Pathological process	proces van pathologische ontwikkeling

SNOMED CT to ICD-10 extended map

Target	Q82.4
Rule	TRUE
Advice	ALWAYS Q82.4 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified