Aplasia of skin	Auditory system hereditary disorder	Autosomal dominant hereditary disorder	Congenital abnormality of external ear	Congenital absence of nipple	Developmental hereditary disorder	Disorder of pinna	Disorder of scalp	Disorder of skin of head	Ectodermal dysplasia	Hereditary disorder of the integument
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Scalp, ear, nipple syndrome (disorder)
	Scalp, ear, nipple syndrome
	Finlay Marks syndrome
	Syndrome with characteristics of the following triad: areas of hairless raw skin over the scalp (present at birth and healing during childhood), prominent hypoplastic ears with almost absent pinna and bilateral amastia. Renal and urinary tract abnormalities, as well as cataract, have also been observed. Transmission is autosomal dominant.
	Finlay-Marks-syndroom
	syndroom van Finlay-Marks

Id	721888002
Status	Primitive

Associated morphology	Hypoplasia
Finding site	Pinna structure
Occurrence	Congenital
Pathological process	Pathological developmental process

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

Associated morphology	Absence
Finding site	Nipple structure
Occurrence	Congenital
Pathological process	Pathological developmental process

Associated morphology	Aplasia
Finding site	Skin structure of scalp
Occurrence	Congenital
Pathological process	Pathological developmental process

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	Q87.8
Rule	TRUE
Advice	ALWAYS Q87.8 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified