Autosomal recessive hereditary disorder	Congenital nephropathy	Congenital neurological disorder	Congenital thrombocytopenia	Disorder of brain	Disorder of thyroid gland	Hereditary disorder of endocrine system	Hereditary disorder of nervous system	Hereditary nephropathy	Hereditary thrombocytopenic disorder
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Thyrocerebrorenal syndrome (disorder)
	Thyrocerebrorenal syndrome
	Cutler Bass Romshe syndrome
	Syndrome with characteristics of renal, neurologic and thyroid disease, associated with thrombocytopenia. It has been described in a brother and his sister. Intelligence was normal. It is transmitted as an autosomal recessive trait.
	syndroom van nefropathie, neuropathie en schildklieraandoening bij trombocytopenie
	thyrocerebrorenaal syndroom

Id	733096007
Status	Primitive

Finding site	Cerebrum
Occurrence	Congenital

Finding site	Thyroid structure
Occurrence	Congenital

Has interpretation	Below reference range
Interprets	Platelet count

Finding site	Kidney structure
Occurrence	Congenital

Has interpretation	Abnormal
Interprets	Hemostatic function

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