Congenital hypergonadotropic hypogonadism	Congenital ichthyosis of skin	Hereditary disorder of endocrine system	Intellectual disability	Multiple system malformation syndrome	Primary hypogonadism	Reproductive system hereditary disorder	Short stature disorder	X-linked recessive hereditary disease
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X-linked intellectual disability, hypogonadism, ichthyosis, obesity, short stature syndrome (disorder)
	X-linked intellectual disability, hypogonadism, ichthyosis, obesity, short stature syndrome
	Young Hughes syndrome
	A rare X-linked intellectual disability syndrome with characteristics of intellectual disability associated with short stature, obesity, primary hypogonadism and an ichthyosiform skin condition. There have been no further descriptions in the literature since 1982.
	X-gebonden syndroom van verstandelijke beperking, hypogonadisme, ichtyose, obesitas en kleine gestalte
	X-gebonden syndroom van mentale retardatie, hypogonadisme, ichtyose, obesitas en kleine gestalte X-gebonden syndroom van verstandelijke handicap, hypogonadisme, ichtyose, obesitas en kleine gestalte syndroom van Young-Hughes

Id	765471005
Status	Primitive

Associated morphology	Hyperkeratosis
Finding site	Entire skin
Occurrence	Congenital
Pathological process	Pathological developmental process

Finding site	Gonadal endocrine structure
Occurrence	Congenital
Pathological process	Pathological developmental process

Has interpretation	Abnormal
Interprets	Keratinization

Interprets

Height / growth measure

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