Autosomal recessive hereditary disorder
Primary immune deficiency disorder
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Predisposition to invasive fungal disease due to caspase recruitment domain family member 9 deficiency (disorder)
Predisposition to invasive fungal disease due to CARD9 deficiency
Invasive candidiasis, deep dermatophytosis syndrome
Predisposition to invasive fungal disease due to caspase recruitment domain family member 9 deficiency
A rare genetic primary immunodeficiency with characteristics of increased susceptibility to fungal infections that typically manifest as recurrent, chronic mucocutaneous candidiasis, systemic candidiasis with meningoencephalitis and deep dermatophytosis. Dermatophytes invade skin, hair, nails, lymph nodes and brain, resulting in erythematosquamous lesions, nodular subcutaneous or ulcerative infiltrations, severe onychomycosis and lymphadenopathy.
predispositie voor invasieve schimmelinfectie door CARD9-deficiëntie
syndroom van invasieve candidose en diepe dermatofytose
aanleg voor invasieve schimmelinfectie door CARD9-deficiëntie
predispositie voor invasieve schimmelinfectie door deficiëntie van 'caspase recruitment domain family member 9'
syndroom van invasieve candidiase en diepe dermatomycose
Id1186719000
StatusPrimitive
Pathological processAbnormal immune process
ICD-10 complex map reference set
TargetD84.8
RuleTRUE
AdviceALWAYS D84.8 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified