Autosomal recessive hereditary disorder	Congenital anomaly of male urogenital tract	Congenital anomaly of urethra	Developmental hereditary disorder	Enzymopathy	Hereditary disorder of the urinary system	Inborn error of metabolism	Male pseudohermaphroditism	Reproductive system hereditary disorder
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3-Oxo-5 alpha-steroid delta 4-dehydrogenase deficiency (disorder)
	3-Oxo-5 alpha-steroid delta 4-dehydrogenase deficiency
	Steroid 5a-reductase deficiency Steroid 5-alpha-reductase deficiency 5-alpha reductase deficiency
	deficiëntie van 5-alfareductase-2
	5-alfareductase-2-deficiëntie

Id	57514000
Status	Primitive

Associated morphology	Morphologically abnormal structure
Finding site	Part of male urethra
Occurrence	Congenital
Pathological process	Pathological developmental process

Associated morphology	Morphologically abnormal structure
Finding site	External genitalia structure
Occurrence	Congenital
Pathological process	Pathological developmental process

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	Q56.1
Rule	TRUE
Advice	ALWAYS Q56.1
Correlation	SNOMED CT source code to target map code correlation not specified