Autosomal recessive hereditary disorder	Congenital anomaly of face bones	Congenital facial dysplasia	Developmental hereditary disorder	Dysostosis	Ectodermal dysplasia with hair-tooth defects	Hereditary disorder of musculoskeletal system	Hereditary disorder of the integument	Hereditary disorder of tooth	Lesion of face	Multiple malformation syndrome with facial defects as major feature
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Teebi Shaltout syndrome (disorder)
	Teebi Shaltout syndrome
	A rare genetic development defect during embryogenesis malformation syndrome with the association of characteristic facial features (including abnormal head shape with narrow forehead, hypertelorism, telecanthus, small earlobes, broad nasal bridge and tip, underdeveloped ala nasi, small/wide mouth and high/cleft palate), ectodermal dysplasia (including oligodontia with delayed dentition, slow growing hair and reduced sweating) and skeletal abnormalities including camptodactyly and caudal appendage. Short stature and abnormal palmar creases are additional clinical features.
	Teebi-Shaltout-syndroom
	syndroom van Teebi-Shaltout

Id	771265006
Status	Primitive

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

Associated morphology	Morphologically abnormal structure
Finding site	Hair 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	Tooth 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