Autosomal recessive hereditary disorder	Developmental hereditary disorder	Digestive system hereditary disorder	Hereditary disorder of the integument	Intellectual disability	Oral-facial-digital syndrome
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Oro-facial digital syndrome type 5 (disorder)
	Oro-facial digital syndrome type 5
	Orofaciodigital syndrome type 5 Thurston syndrome Orofaciodigital syndrome Thurston type
	Syndrome with characteristics of median cleft of upper lip, postaxial polydactyly of hands and feet and oral manifestations (duplicated frenulum). Less than 20 patients (predominantly of Indian origin) have been reported so far. Autosomal recessive inheritance has been suggested, but the causative gene has not yet been identified.
	orofaciodigitaal syndroom type 5
	OFD5 syndroom van postaxiale polydactylie en mediane splijting van bovenlip orofaciodigitaal syndroom Thurston-type syndroom van Thurston

Id	722105002
Status	Primitive

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

Associated morphology	Dysplasia
Finding site	Ectoderm structure
Occurrence	Congenital
Pathological process	Pathological developmental process

Associated morphology	Morphologically abnormal structure
Finding site	Structure of internal part of mouth
Occurrence	Congenital
Pathological process	Pathological developmental process

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

Associated morphology	Morphologically abnormal structure
Finding site	Digit 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 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified