Autosomal recessive hereditary disorder	Developmental hereditary disorder	Disorder of digestive system specific to fetus OR newborn	Hereditary gingival fibromatosis	Multiple malformation syndrome with facial defects as major feature
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Gingival fibromatosis with facial dysmorphism syndrome (disorder)
	Gingival fibromatosis with facial dysmorphism syndrome
	A very rare syndrome characterized by the association of gingival fibromatosis and craniofacial dysmorphism.

Id	719687007
Status	Primitive

Associated morphology	Fibromatosis
Finding site	Gingival structure
Pathological process	Pathological developmental process

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

SNOMED CT to Orphanet simple map

RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set

Target	Q87.0
Term	Congenitale gestoorde-ontwikkelingssyndromen waarbij voornamelijk aangezicht is aangedaan

SNOMED CT to ICD-10 extended map

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