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Ellis-Van Creveld Syndrome MeSH Descriptor Data 2022


MeSH Heading
Ellis-Van Creveld Syndrome
Tree Number(s)
C05.116.099.708.327
C16.131.077.350.398
C16.131.831.350.398
C16.320.850.250.398
C17.800.804.350.398
C17.800.827.250.398
Unique ID
D004613
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D004613
Annotation
do not use /‌congen & do not coord with INFANT, NEWBORN, DISEASES
Scope Note
Dwarfism occurring in association with defective development of skin, hair, and teeth, polydactyly, and defect of the cardiac septum. (Dorland, 27th ed)
Entry Term(s)
Chondroectodermal Dysplasia
Ellis-Van Creveld Dysplasia
Mesoectodermal Dysplasia
Public MeSH Note
65
History Note
65(63)
Date Established
1965/01/01
Date of Entry
1999/01/01
Revision Date
2016/01/20
Ellis-Van Creveld Syndrome Preferred
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