Autosomal recessive hereditary disorder	Developmental hereditary disorder	Syndactyly
\|	\|	\|

Mesoaxial synostotic syndactyly with phalangeal reduction syndrome (disorder)
	Mesoaxial synostotic syndactyly with phalangeal reduction syndrome
	Syndactyly Malik Percin type Syndactyly type 9
	A novel and distinct form of non-syndromic syndactyly including complete syndactyly of the third and fourth fingers with synostoses of the corresponding metacarpals and associated single phalanges, syndactyly of the second and third toes and fifth finger clinodactyly. It has been described in two families. The locus for this complex limb malformation was mapped to chromosome 17p13.3. The condition is transmitted as an autosomal recessive trait.
	mesoaxiale synostotische syndactylie met falangeale reductie
	MSSD syndactylie type 9 syndactylie type Malik-Percin

Id	724170007
Status	Primitive

Associated morphology	Congenital abnormal fusion
Finding site	Digit structure
Occurrence	Congenital
Pathological process	Pathological developmental process

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	Q70.0
Rule	TRUE
Advice	ALWAYS Q70.0 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified

Target	Q70.2
Rule	TRUE
Advice	ALWAYS Q70.2
Correlation	SNOMED CT source code to target map code correlation not specified