Autosomal recessive hereditary disorder	Congenital alopecia	Congenital neurological disorder	Developmental hereditary disorder	Epilepsy	Hereditary disorder of nervous system	Hereditary disorder of the integument	Intellectual disability
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Alopecia, epilepsy, intellectual disability syndrome Moynahan type (disorder)
	Alopecia, epilepsy, intellectual disability syndrome Moynahan type
	Moynahan syndrome
	A rare genetic epilepsy syndrome with characteristics of congenital alopecia, early-onset epilepsy, intellectual disability and speech delay. Large stature, delayed bone development and abnormal electroencephalogram have also been associated.
	syndroom van alopecia, epilepsie en verstandelijke beperking Moynahan-type

Id	788417006
Status	Primitive

Associated morphology	Absence
Finding site	Hair structure
Occurrence	Congenital
Pathological process	Pathological developmental process

Finding site	Cerebrum
Pathological process	Pathological developmental process

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	G40.4
Rule	TRUE
Advice	ALWAYS G40.4 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified