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Cranioectodermal Dysplasia MeSH Supplementary Concept Data 2024


MeSH Supplementary
Cranioectodermal Dysplasia
Unique ID
C562966
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C562966
Entry Term(s)
Levin Syndrome I
Sensenbrenner Syndrome
Registry Number
0
Heading Mapped to
Bone and Bones / *abnormalities
*Craniosynostoses
*Ectodermal Dysplasia
Frequency
29
Note
mutation in IFT122
Date of Entry
2012/11/05
Revision Date
2013/11/06
Cranioectodermal Dysplasia Preferred
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