Autosomal dominant hereditary disorder	Congenital alopecia	Congenital hypogonadotropic hypogonadism	Developmental hereditary disorder	Hereditary disorder of endocrine system	Hereditary disorder of nervous system	Hereditary disorder of the integument	Reproductive system hereditary disorder
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Hypogonadotropic hypogonadism with frontoparietal alopecia syndrome (disorder)
	Hypogonadotropic hypogonadism with frontoparietal alopecia syndrome
	Salti Salem syndrome
	Syndrome with the association of hypogonadotropic hypogonadism and frontoparietal alopecia. It has been described in six members (four males and two females) of a consanguineous Lebanese family. In addition to frontoparietal alopecia, the remaining scalp hair was also sparse and axillary and pubic hair was absent. Despite the family history of consanguinity, autosomal dominant inheritance with reduced penetrance was considered as the most likely mode of transmission.
	syndroom van hypogonadotroop hypogonadisme en frontopariëtale alopecie

Id	721842008
Status	Primitive

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

Finding site	Gonadal endocrine structure
Occurrence	Congenital

Finding site	Structure of distal part of pituitary
Occurrence	Congenital

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	E23.0
Rule	TRUE
Advice	ALWAYS E23.0
Correlation	SNOMED CT source code to target map code correlation not specified

Target	L65.9
Rule	TRUE
Advice	ALWAYS L65.9
Correlation	SNOMED CT source code to target map code correlation not specified