An instance of Chilblain lupus that is caused by an inherited modification of the individual's genome.
Comprehensive, easy-to-understand information about this condition
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Ewing sarcoma of bone
MONDO:0002625
hereditary multiple osteochondromas
MONDO:0005508
acroosteolysis dominant type
MONDO:0007057
diaphyseal medullary stenosis-bone malignancy syndrome
MONDO:0007205
cherubism
MONDO:0007315
chondrocalcinosis 2
MONDO:0007319