Tumoral Calcinosis, Normophosphatemic, Familial MeSH Supplementary Concept Data 2024

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Concepts

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 Number: 0
Heading Mapped to: *Calcinosis; *Hyperostosis, Cortical, Congenital
Frequency: 2
Note: mutatins in SAMD9
Date of Entry: 2012/11/05

Tumoral Calcinosis, Normophosphatemic, Familial Preferred

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