NLM Logo

Cerebellar Vermis Aplasia with Associated Features suggesting Smith-Lemli-Opitz Syndrome and Meckel Syndrome MeSH Supplementary Concept Data 2025


MeSH Supplementary
Cerebellar Vermis Aplasia with Associated Features suggesting Smith-Lemli-Opitz Syndrome and Meckel Syndrome
Unique ID
C565867
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C565867
Registry Numbers
0
Heading Mapped to
*Cerebellar Diseases
Cerebellum / abnormalities
*Encephalocele
*Polycystic Kidney Diseases
*Meningocele
*Smith-Lemli-Opitz Syndrome
Frequency
0
Date of Entry
2012/11/05
Revision Date
2013/11/06
Cerebellar Vermis Aplasia with Associated Features suggesting Smith-Lemli-Opitz Syndrome and Meckel Syndrome Preferred
page delivered in 0.003s