Autosomal recessive ichthyosis	Congenital nephropathy	Hereditary nephropathy	Intellectual disability	Multiple system malformation syndrome	Renal impairment	Short stature disorder
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Ichthyosis, intellectual disability, dwarfism, renal impairment syndrome (disorder)
	Ichthyosis, intellectual disability, dwarfism, renal impairment syndrome
	Passwell Goodman Siprkowski syndrome
	Syndrome with characteristics of nonbullous congenital ichthyosis, intellectual deficit, dwarfism and renal impairment. It has been described in four members of one Iranian family. Transmission is autosomal recessive.
	syndroom van ichtyose, verstandelijke beperking, dwerggroei en nierfunctiestoornis
	syndroom van ichtyose, verstandelijke handicap, dwerggroei en nierfunctiestoornis syndroom van ichtyose, mentale retardatie, dwerggroei en nierfunctiestoornis syndroom van Passwell-Goodman-Siprkowski

Id	733097003
Status	Primitive

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

Has interpretation	Impaired
Interprets	Measurement of renal function

Finding site	Kidney 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	Q80.9
Rule	TRUE
Advice	ALWAYS Q80.9 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified

Target	F79.9
Rule	TRUE
Advice	ALWAYS F79.9
Correlation	SNOMED CT source code to target map code correlation not specified

Target	E34.3
Rule	TRUE
Advice	ALWAYS E34.3
Correlation	SNOMED CT source code to target map code correlation not specified

Target	N19
Rule	TRUE
Advice	ALWAYS N19
Correlation	SNOMED CT source code to target map code correlation not specified