MeSH Browser

MeSH Supplementary: Megarbane Jalkh Syndrome
Unique ID: C548071
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C548071
Entry Term(s): Developmental Delay, Dysmorphic Features, Neonatal Spontaneous Fractures, Wrinkled Skin, And Hepatic Failure; Megarbane-Jalkh Syndrome
Registry Numbers: 0
Heading Mapped to: *Abnormalities, Multiple
Frequency: 0
Source: Am. J. Med. Genet. 146A: 3198-3201
Date of Entry: 2010/08/25
Revision Date: 2012/11/30

Megarbane Jalkh Syndrome MeSH Supplementary Concept Data 2025