MeSH Browser

MeSH Supplementary: Meckel syndrome type 2
Unique ID: C536131
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536131
Entry Term(s): Meckel Syndrome, Type 2; Meckel-Gruber Syndrome, Type 2
Registry Numbers: 0
Heading Mapped to: *Ciliary Motility Disorders; *Encephalocele; *Polycystic Kidney Diseases
Frequency: 0
Note: mutation in TMEM216
Date of Entry: 2010/08/25
Revision Date: 2012/11/05

Meckel syndrome type 2 MeSH Supplementary Concept Data 2025