MeSH Browser

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 Numbers: 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 MeSH Supplementary Concept Data 2025