Autosomal recessive hereditary disorder	Developmental hereditary disorder	Ectodermal dysplasia	Hereditary disorder of the integument	Intellectual disability	Multiple malformation syndrome with facial-limb defects as major feature
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Alopecia, contracture, dwarfism, intellectual disability syndrome (disorder)
	Alopecia, contracture, dwarfism, intellectual disability syndrome
	ACD (alopecia, contracture, dwarfism) syndrome ACD (alopecia, contracture, dwarfism) mental retardation syndrome
	A form of ectodermal dysplasia syndrome with characteristics of short stature of prenatal onset, alopecia, ichthyosis, photophobia, ectrodactyly, seizures, scoliosis, multiple contractures, fusions of various bones, particularly elbows, carpals, metacarpals, and spine, intellectual disability and facial dysmorphism.
	syndroom van alopecia, contractuur, dwerggroei en verstandelijke beperking
	syndroom van alopecia, contractuur, dwerggroei en mentale retardatie ACD-syndroom syndroom van alopecia, contractuur, dwerggroei en verstandelijke handicap

Id	720979002
Status	Primitive

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

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

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