Congenital anomaly of hair	Hereditary disorder of musculoskeletal system	Inherited cutaneous hyperpigmentation	Osteopathia striata	White forelock
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Osteopathia striata, pigmentary dermopathy, white forelock syndrome (disorder)
	Osteopathia striata, pigmentary dermopathy, white forelock syndrome
	Whyte Murphy syndrome
	Syndrome with characteristics of the association of osteopathia striata (longitudinal striations through most of the long bones) with a macular hyperpigmented dermopathy and a white forelock. It has been observed in a woman and her two daughters, whereas her son is unaffected. X-linked or autosomal dominant inheritance is proposed.
	syndroom van osteopathia striata, pigmentaire dermatopathie en poliosis circumscripta
	syndroom van osteopathia striata, pigmentaire dermatopathie en witte haarlok

Id	787408008
Status	Primitive

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

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

Has interpretation	Above reference range
Interprets	Bone density scan

Associated morphology	Hyperpigmentation
Finding site	Skin structure
Occurrence	Congenital
Pathological process	Pathological developmental process

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

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