Congenital anomaly of skeletal muscle	Multiple malformation syndrome with facial defects as major feature
\|	\|

Congenital nonprogressive myopathy with Moebius and Robin sequences (disorder)
	Congenital nonprogressive myopathy with Moebius and Robin sequences
	Carey Fineman Ziter syndrome
	syndroom van congenitale niet-progressieve myopathie met Möbius- en Robin-sequentie
	syndroom van congenitale niet-progressieve myopathie met Moebius- en Robin-sequentie syndroom van congenitale niet-progressieve myopathie met micrognathie, palatoschisis, glossoptose en verlamming van zesde en zevende hersenzenuw Carey-Fineman-Ziter-syndroom syndroom van Carey-Fineman-Ziter syndroom van congenitale niet-progressieve myopathie met micrognathie, palatoschisis, glossoptosis en verlamming van hersenzenuw VI en VII syndroom van congenitale niet-progressieve myopathie met micrognathie, palatoschisis, glossoptosis en verlamming van nervus abducens en facialis

Id	429753001
Status	Primitive

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

Associated morphology	Morphologically abnormal structure
Finding site	Face structure
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
Correlation	SNOMED CT source code to target map code correlation not specified