Familial monosomy 7 syndrome

Synonyms: Monosomy 7 myelodysplasia and leukemia syndrome

Summary

A rare neoplastic disease characterized by infantile to childhood onset of evidence of bone marrow insufficiency/failure associated with increased risk for myelodysplastic syndrome or acute myeloid leukemia. Most patients present with petechiae, easy bruising, or anemia. Rapid progression is common, and prognosis is generally poor. [from ORDO]

Available tests

8 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (8 available)

Cytogenetics Tests

Karyotyping (8)

Genes See tests for all associated and related genes

Related genes Help
Genes reported to contribute to conditions that are children of this condition in a hierarchy.

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