Congenital abnormality of skull shape	Congenital deformity	Congenital musculoskeletal deformity	Developmental hereditary disorder	Hereditary disorder of musculoskeletal system	Intellectual disability	Multiple malformation syndrome with facial defects as major feature	Plagiocephaly	X-linked recessive hereditary disease
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X-linked intellectual disability with plagiocephaly syndrome (disorder)
	X-linked intellectual disability with plagiocephaly syndrome
	Hyde Forster McCarthy Berry syndrome
	This syndrome has characteristics of severe intellectual deficit, brachycephaly, plagiocephaly, prominent forehead and coarse facial features. It has been described in two males from one family. Two females belonging to the same family displayed moderate intellectual deficit but no craniofacial dysmorphism.
	X-gebonden syndroom van verstandelijke beperking en plagiocefalie
	X-gebonden syndroom van mentale retardatie en plagiocefalie X-gebonden syndroom van verstandelijke handicap en plagiocefalie syndroom van Hyde Forster-McCarthy-Berry

Id	719812008
Status	Primitive

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

Associated morphology	Deformity
Finding site	Bone structure of cranium
Occurrence	Congenital
Pathological process	Pathological developmental process

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	Q87.0
Rule	TRUE
Advice	ALWAYS Q87.0 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified