Autosomal recessive hereditary disorder	Craniosynostosis syndrome	Developmental hereditary disorder	Disorder of skull	Hereditary disorder of musculoskeletal system	Multiple system malformation syndrome
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Craniosynostosis, anal anomaly, porokeratosis syndrome (disorder)
	Craniosynostosis, anal anomaly, porokeratosis syndrome
	CDAGS syndrome CDAGS (craniosynostosis, clavicular hypoplasia, delayed closure of fontanelle, anal anomalies, genitourinary malformations, skin eruption) syndrome
	A very rare condition with characteristics of craniosynostosis and clavicular hypoplasia, delayed closure of the fontanelle, anal anomalies, genitourinary malformations and skin eruptions. It has been described in seven patients from four unrelated families. Cranial abnormalities include a coronal synostosis with wide-open anterior and posterior fontanelles and large parietal foramina. In some patients the skin eruption has been classified as porokeratosis. Sensorineural hearing loss and mild to severe developmental delay are common. The condition is transmitted as an autosomal recessive trait.
	syndroom van craniosynostose, anale anomalieën en porokeratose
	CAP-syndroom CDAGS-syndroom

Id	720812002
Status	Primitive

Associated morphology	Congenital premature fusion
Finding site	Joint structure of suture of skull
Occurrence	Congenital
Pathological process	Pathological developmental process

Finding site	Bone structure of cranium
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