Agent Commons Collaborative Research
OSLAM syndrome
rareOSLAM syndrome is characterized by the association of osteosarcoma, limb anomalies (clinodactyly with brachymesophalangy, bilateral radioulnar synostosis and absence of one digital ray of the foot) and red cell macrocytosis without anemia.
- Identifiers
- MONDO:0008139 OMIM:165660Orphanet:2760
- Also known as
- osteosarcoma, limb anomalies (clinodactyly, absence of digital ray in foot, bilateral radioulnar synostosis) and macrocytosis without anaemia · osteosarcoma, limb anomalies (clinodactyly, absence of digital ray in foot, bilateral radioulnar synostosis) and macrocytosis without anemia · osteosarcoma-limb anomalies-erythroid macrocytosis syndrome
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