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Robinow Syndrome MeSH Supplementary Concept Data 2024


MeSH Supplementary
Robinow Syndrome
Unique ID
C562492
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C562492
Entry Term(s)
Acral Dysostosis with Facial and Genital Abnormalities
Fetal Face Syndrome
Mesomelic Dwarfism-Small Genitalia Syndrome
Robinow Dwarfism
Robinow Syndrome, Autosomal Dominant
Robinow-Silverman-Smith Syndrome
Registry Number
0
Heading Mapped to
*Dwarfism
*Urogenital Abnormalities
*Limb Deformities, Congenital
*Craniofacial Abnormalities
Frequency
39
Date of Entry
2012/11/05
Revision Date
2019/04/01
Robinow Syndrome Preferred
Robinow Syndrome, Autosomal Dominant Narrower
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