Autosomal dominant hereditary disorder	Cleft palate	Congenital alopecia	Congenital retrognathism	Developmental hereditary disorder	Hereditary disorder of musculoskeletal system	Hereditary disorder of the integument	Multiple system malformation syndrome	Poikiloderma
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Poikiloderma, alopecia, retrognathism, cleft palate syndrome (disorder)
	Poikiloderma, alopecia, retrognathism, cleft palate syndrome
	PARC (poikiloderma, alopecia, retrognathism, cleft palate) syndrome PARC syndrome
	A rare genetic developmental defect during embryogenesis. A syndrome characterized by the association of congenital poikiloderma (P), generalized alopecia (A), retrognathism (R) and cleft palate (C). There have been no further descriptions in the literature since 1990.
	syndroom van poikilodermie, alopecia, retrognathie en palatoschisis
	syndroom van poikilodermie, alopecia, retrognathie en gespleten gehemelte PARC-syndroom

Id	771186004
Status	Primitive

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

Associated morphology	Poikiloderma
Finding site	Skin structure
Occurrence	Congenital
Pathological process	Pathological developmental process

Associated morphology	Developmental failure of fusion
Finding site	Palatal structure
Occurrence	Congenital
Pathological process	Pathological developmental process

Associated morphology	Posterior displacement
Finding site	Bone structure of jaw
Occurrence	Congenital
Pathological process	Pathological developmental process

Associated morphology	Recession
Finding site	Bone structure of jaw
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