Autosomal dominant hereditary disorder	Congenital anomaly of limb	Developmental hereditary disorder	Hereditary disorder of musculoskeletal system	Hereditary red blood cell disorder	Macrocytosis - no anemia	Multiple malformation syndrome with limb defect as major feature	Osteosarcoma of bone
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Osteosarcoma, limb anomalies, erythroid macrocytosis syndrome (disorder)
	Osteosarcoma, limb anomalies, erythroid macrocytosis syndrome
	OSLAM syndrome OSLAM (osteosarcoma, limb anomalies, erythroid macrocytosis) syndrome
	Syndrome characterized by the association of osteosarcoma, limb anomalies (clinodactyly with brachymesophalangia, bilateral radioulnar synostosis and absence of one digital ray of the foot) and red cell macrocytosis without anemia. It has been described in three out of nine children from one family.
	syndroom van osteosarcoom, misvorming van extremiteit en erytroïde macrocytemie

Id	733064004
Status	Primitive

Associated morphology	Osteosarcoma
Finding site	Bone structure

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

Finding site	Erythrocyte
Occurrence	Congenital
Pathological process	Pathological developmental process

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	C41.9
Rule	TRUE
Advice	ALWAYS C41.9 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION \| POSSIBLE REQUIREMENT FOR MORPHOLOGY CODE
Correlation	SNOMED CT source code to target map code correlation not specified

Target	Q74.8
Rule	TRUE
Advice	ALWAYS Q74.8
Correlation	SNOMED CT source code to target map code correlation not specified

Target	D75.8
Rule	TRUE
Advice	ALWAYS D75.8
Correlation	SNOMED CT source code to target map code correlation not specified