Autosomal recessive hereditary disorder	Benign neoplasm of skin of face	Congenital microcephaly	Developmental hereditary disorder	Hereditary disorder of nervous system	Hereditary disorder of the integument	Hypoplasia of corpus callosum	Intellectual disability	Mass of preauricular region	Multiple system malformation syndrome	Skin tag
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Intellectual disability, hypoplastic corpus callosum, preauricular tag syndrome (disorder)
	Intellectual disability, hypoplastic corpus callosum, preauricular tag syndrome
	Da Silva syndrome
	This syndrome has characteristics of hypoplastic corpus callosum, microcephaly, severe intellectual deficit, preauricular skin tags, camptodactyly, growth retardation, and recurrent bronchopneumonia. It has been described in four patients in two families. Transmission is autosomal recessive.
	syndroom van verstandelijke beperking, hypoplastische corpus callosum en bijoortje
	syndroom van verstandelijke handicap, hypoplastische corpus callosum en bijoortje syndroom van mentale retardatie, hypoplastische corpus callosum en bijoortje syndroom van Da Silva

Id	722455002
Status	Primitive

Associated morphology	Fibroepithelial polyp
Finding site	Skin structure of preauricular region
Occurrence	Congenital

Associated morphology	Hypoplasia
Finding site	Corpus callosum structure
Occurrence	Congenital
Pathological process	Pathological developmental process

Associated morphology	Congenital smallness
Finding site	Head structure
Occurrence	Congenital
Pathological process	Pathological developmental process

Has interpretation	Below reference range
Interprets	Birth head circumference

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