Autosomal recessive hereditary disorder	Congenital anomaly of the kidney	Congenital microcephaly	Congenital nephritis	Developmental hereditary disorder	Hereditary nephritis	Intellectual disability	Marfanoid physique	Multiple system malformation syndrome
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Microcephalus, glomerulonephritis, marfanoid habitus syndrome (disorder)
	Microcephalus, glomerulonephritis, marfanoid habitus syndrome
	Syndrome with characteristics of intellectual deficit, marfanoid habitus, microcephaly, and glomerulonephritis. It has been described in two sisters.
	syndroom van microcefalie, glomerulonefritis en marfanoïde habitus

Id	733472005
Status	Primitive

Interprets

Associated morphology	Congenital smallness
Finding site	Head structure
Occurrence	Congenital
Pathological process	Pathological developmental process

Associated morphology	Chronic inflammation
Finding site	Glomerulus structure
Occurrence	Congenital
Pathological process	Pathological developmental process

Has interpretation	Below reference range
Interprets	Birth head circumference

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