Congenital hypogonadotropic hypogonadism	Hereditary disorder of endocrine system	Hereditary disorder of nervous system	Reproductive system hereditary disorder	Retinitis pigmentosa
\|	\|	\|	\|	\|

Hypogonadotropic hypogonadism retinitis pigmentosa syndrome (disorder)
	Hypogonadotropic hypogonadism retinitis pigmentosa syndrome
	Chang Davidson Carlson syndrome
	This syndrome is characterized by the association of hypogonadotropic hypogonadism (with primary amenorrhea and lack of secondary sexual development) and retinitis pigmentosa. It has been described in two sisters born to nonconsanguineous parents.
	syndroom van hypogonadotroop hypogonadisme en retinitis pigmentosa

Id	733113002
Status	Primitive

Associated morphology	Dystrophy
Finding site	Retinal structure
Occurrence	Congenital

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 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified

Target	H35.5
Rule	TRUE
Advice	ALWAYS H35.5
Correlation	SNOMED CT source code to target map code correlation not specified