Congenital anomaly of skin	Developmental hereditary disorder	Hereditary disorder of the integument	Multiple system malformation syndrome	X-linked dominant hereditary disease
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Focal dermal hypoplasia (disorder)
	Focal dermal hypoplasia
	Goltz-Gorlin syndrome FDH - Focal dermal hypoplasia Goltz syndrome FODH - Focal dermal hypoplasia
	focale dermale hypoplasie
	syndroom van Goltz

Id	205573006
Status	Primitive

Associated morphology	Morphologically abnormal structure
Finding site	Skin structure
Occurrence	Congenital
Pathological process	Pathological developmental process

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	Q82.8
Rule	TRUE
Advice	ALWAYS Q82.8
Correlation	SNOMED CT source code to target map code correlation not specified