Autosomal dominant hereditary disorder	Chronic glomerulonephritis	Congenital anomaly of skeletal bone	Congenital anomaly of the kidney	Congenital nephritis	Developmental hereditary disorder	Hereditary disorder of musculoskeletal system	Hereditary nephritis	Mesomelic dysplasia	Multiple system malformation syndrome
\|	\|	\|	\|	\|	\|	\|	\|	\|	\|

Dyschondrosteosis and nephritis syndrome (disorder)
	Dyschondrosteosis and nephritis syndrome
	The association of short stature due to mesomelic shortening of the limbs and Madelung deformity with hereditary nephritis. The syndrome was originally described in male and female members from four generations of one large kindred. The females appeared to be more severely affected than the males, with a sex ratio (female to male) of 4:1. The skeletal anomalies closely resembled those of Leri-Weill dyschondrosteosis. The mode of transmission was reported as autosomal dominant.
	syndroom van dyschondrosteose en nefritis

Id	722433005
Status	Primitive

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

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

Clinical course

Interprets

Height / growth measure

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