Autosomal recessive ichthyosis	Keratitis ichthyosis and deafness syndrome
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Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder)
	Autosomal recessive keratitis-ichthyosis-deafness syndrome
	Autosomal recessive KID (keratitis, ichthyosis, deafness) syndrome
	autosomaal recessief keratitis-ichthyosis-doofheid-syndroom
	autosomaal recessief KID-syndroom syndroom met autosomaal recessieve keratitis, ichtyosis en doofheid

Id	403780007
Status	Primitive

Associated morphology	Hyperkeratosis
Finding site	Entire skin
Occurrence	Congenital
Pathological process	Pathological developmental process

Has interpretation	Abnormal
Interprets	Keratinization

Finding site	Structure of auditory system
Occurrence	Congenital
Pathological process	Pathological developmental process

Associated morphology	Dysplasia
Finding site	Ectoderm structure
Occurrence	Congenital
Pathological process	Pathological developmental process

Interprets

ICD-10 complex map reference set

Target	Q87.8
Rule	TRUE
Advice	ALWAYS Q87.8
Correlation	SNOMED CT source code to target map code correlation not specified