Congenital abnormality of skull and face bones	Ectodermal dysplasia with hair-tooth defects	Hereditary disorder of musculoskeletal system	Hereditary disorder of the integument	Hereditary disorder of tooth	Inherited arthrogryposis	Intellectual disability	Multiple malformation syndrome with facial defects as major feature	Orofacial cleft
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Contracture with ectodermal dysplasia and orofacial cleft syndrome (disorder)
	Contracture with ectodermal dysplasia and orofacial cleft syndrome
	Ladda Zonana Ramer syndrome
	An ectodermal dysplasia syndrome with characteristics of severe arthrogryposis, multiple ectodermal dysplasia features, cleft lip/palate, facial dysmorphism, growth deficiency and a moderate delay of psychomotor development. Ectodermal dysplasia manifestations include sparse, brittle and hypopigmented hair, xerosis, multiple nevi, small conical shaped teeth and hypodontia, and facial dysmorphism with blepharophimosis, deep-set eyes and micrognathia.
	syndroom van contracturen, ectodermale dysplasie en cheilopalatoschisis
	syndroom van contracturen, ectodermale dysplasie en gespleten gehemelte met gespleten lip syndroom van Ladda-Zonana-Ramer

Id	720746006
Status	Primitive

Associated morphology	Morphologically abnormal structure
Finding site	Hair structure
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	Developmental failure of fusion
Finding site	Bone structure of head
Occurrence	Congenital
Pathological process	Pathological developmental process

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

Associated morphology	Developmental failure of fusion
Finding site	Structure of subregion of head
Occurrence	Congenital
Pathological process	Pathological developmental process

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

Associated morphology	Contracture
Finding site	Structure of joint region
Occurrence	Congenital
Pathological process	Pathological developmental process

Has interpretation	Decreased
Interprets	Range of joint movement

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	Q87.8
Rule	TRUE
Advice	ALWAYS Q87.8 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified