Autosomal recessive hereditary disorder	Developmental hereditary disorder	Hereditary nephropathy	Multiple malformation syndrome with facial-limb defects as major feature	Renal dysplasia
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Renal dysplasia with limb defect syndrome (disorder)
	Ulbright Hodes syndrome
	Renal dysplasia with limb defect syndrome Renal dysplasia, mesomelia, radiohumeral fusion syndrome
	Syndrome with characteristics of renal dysplasia, growth retardation, phocomelia or mesomelia, radiohumeral fusion, rib abnormalities, anomalies of the external genitalia and a potter-like facies. The syndrome has been described in three infants, all of whom died shortly after birth from respiratory distress resulting from pulmonary hypoplasia and oligohydramnios caused by renal dysplasia. The mode of transmission appears to be autosomal recessive.
	syndroom van dysplasie van nier en defect van extremiteit
	syndroom van nierdysplasie en ledemaatdefecten syndroom van Ulbright-Hodes syndroom van renale dysplasie en defect van extremiteit Ulbright-Hodes-syndroom

Id	719840003
Status	Primitive

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

Associated morphology	Dysplasia
Finding site	Kidney structure
Occurrence	Congenital
Pathological process	Pathological developmental process

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

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