Autosomal recessive hereditary disorder	Calcification of basal ganglia	Congenital neurological disorder	Developmental hereditary disorder	Disorder of cerebral cortex	Hereditary degenerative disease of central nervous system	Multiple system malformation syndrome
\|	\|	\|	\|	\|	\|	\|

Brain calcification Rajab type (disorder)
	Brain calcification Rajab type
	Rajab syndrome
	An inherited disorder with characteristics of widespread calcifications of the basal ganglia and cortex, developmental delay, small stature, retinopathy and microcephaly. The absence of progressive deterioration of the neurological functions is characteristic of the disease. The syndrome has been described in eight children from two interrelated families. The disorder is associated with a genetic locus on chromosome 2 and transmission is autosomal recessive.
	cerebrale calcificatie van Rajab-type
	hersencalcinose van Rajab-type

Id	720576001
Status	Primitive

Associated morphology	Pathologic calcification
Finding site	Basal ganglion structure
Pathological process	Pathological developmental process

Associated morphology	Pathologic calcification
Finding site	Structure of cerebral cortex
Pathological process	Pathological developmental process

Associated morphology	Morphologically abnormal structure
Occurrence	Congenital
Pathological process	Pathological developmental process

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	G93.8
Rule	TRUE
Advice	ALWAYS G93.8 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified