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Tumoral Calcinosis, Normophosphatemic, Familial MeSH Supplementary Concept Data 2025


MeSH Supplementary
Tumoral Calcinosis, Normophosphatemic, Familial
Unique ID
C566473
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C566473
Entry Term(s)
Calcinosis, Tumoral, With Normophosphatemia
Registry Numbers
0
Heading Mapped to
*Calcinosis
*Hyperostosis, Cortical, Congenital
Frequency
2
Note
mutatins in SAMD9
Date of Entry
2012/11/05
Revision Date
1955/01/01
Tumoral Calcinosis, Normophosphatemic, Familial Preferred
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