Congenital cleft larynx	Developmental hereditary disorder	Hereditary disorder of the urinary system	Multiple malformation syndrome, moderate short stature, facial	Penile hypospadias	Reproductive system hereditary disorder	Sex-linked hereditary disorder
\|	\|	\|	\|	\|	\|	\|

Opitz-Frias syndrome (disorder)
	Opitz-Frias syndrome
	Opitz syndrome G syndrome Congenital cleft larynx and Opitz-Frias syndrome Hypertelorism-hypospadias syndrome Opitz's (J.M.) syndrome
	X-gebonden Opitz G/BBB-syndroom
	Opitz G-syndroom syndroom van hypertelorisme, oesofageale abnormaliteit en hypospadie syndroom van Opitz syndroom van Opitz-Frias hypertelorisme-oesofageale abnormaliteit-hypospadie-syndroom

Id	81771002
Status	Primitive

Associated morphology	Developmental failure of fusion
Finding site	Laryngeal structure
Occurrence	Congenital
Pathological process	Pathological developmental process

Associated morphology	Morphologically abnormal structure
Finding site	Structure of urethral aspect of penis
Occurrence	Congenital
Pathological process	Pathological developmental process

Associated morphology	Malposition
Finding site	Male external urethral orifice
Occurrence	Congenital
Pathological process	Pathological developmental process

PALGA thesaurus simple reference set for pathology

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	Q87.8
Rule	TRUE
Advice	ALWAYS Q87.8
Correlation	SNOMED CT source code to target map code correlation not specified