congenitale afwijking van haar	hereditaire aandoening van bewegingsapparaat	hereditaire cutane hyperpigmentatie	osteopathia striata	poliosis circumscripta
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syndroom van osteopathia striata, pigmentaire dermatopathie en poliosis circumscripta (aandoening)
	syndroom van osteopathia striata, pigmentaire dermatopathie en poliosis circumscripta
	syndroom van osteopathia striata, pigmentaire dermatopathie en witte haarlok
	Osteopathia striata, pigmentary dermopathy, white forelock syndrome
	Whyte Murphy syndrome
	A rare primary bone dysplasia characterized by the association of osteopathia striata (longitudinal striations through most of the long bones) with a macular, hyperpigmented dermopathy and a white forelock.

Id	787408008
Status	Primitive

Associated morphology	dysplasie
Finding site	botstructuur
Occurrence	congenitaal
Pathological process	proces van pathologische ontwikkeling

Associated morphology	morfologische afwijking
Finding site	structuur van pilus
Occurrence	congenitaal
Pathological process	proces van pathologische ontwikkeling

Has interpretation	boven referentiebereik
Interprets	botdensitometrie

Associated morphology	hyperpigmentatie
Finding site	structuur van huid
Occurrence	congenitaal
Pathological process	proces van pathologische ontwikkeling

DHD Diagnosis thesaurus reference set

RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set

Target	Q77.8
Term	Overige gespecificeerde vormen van osteochondrodysplasie met groeistoornissen van pijpbeenderen en wervelkolom

SNOMED CT to Orphanet simple map

2779

SNOMED CT to ICD-10 extended map

Target	Q77.8
Rule	TRUE
Advice	ALWAYS Q77.8 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified