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Polycystic Kidney Disease, Potter Type I, with Microbrachycephaly, Hypertelorism, and Brachymelia MeSH Supplementary Concept Data 2024


MeSH Supplementary
Polycystic Kidney Disease, Potter Type I, with Microbrachycephaly, Hypertelorism, and Brachymelia
Unique ID
C564881
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C564881
Registry Number
0
Heading Mapped to
*Abnormalities, Multiple
*Craniosynostoses
*Ectromelia
*Hypertelorism
*Polycystic Kidney, Autosomal Recessive
Frequency
0
Date of Entry
2012/11/05
Polycystic Kidney Disease, Potter Type I, with Microbrachycephaly, Hypertelorism, and Brachymelia Preferred
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