Short Rib-Polydactyly Syndrome
"Short Rib-Polydactyly Syndrome" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A syndrome inherited as an autosomal recessive trait and incompatible with life. The main features are narrow thorax, short ribs, scapular and pelvic dysplasia, and polydactyly.
| Descriptor ID |
D012779
|
| MeSH Number(s) |
C05.116.099.708.857 C05.660.585.600.750 C16.131.077.850 C16.131.621.585.600.750
|
| Concept/Terms |
Saldino-Noonan Syndrome- Saldino-Noonan Syndrome
- Saldino Noonan Syndrome
- Polydactyly with Neonatal Chondrodystrophy, Type 1
- Short Rib-Polydactyly Syndrome, Type I
- Short Rib Polydactyly Syndrome, Type I
- Asphyxiating Thoracic Dystrophy 3
- Polydactyly With Neonatal Chondrodystrophy, Type I
- Short Rib-Polydactyly Syndrome, Saldino-Noonan Type
- Short Rib Polydactyly Syndrome, Saldino Noonan Type
- Short Rib-Polydactyly Syndrome Type 1
- Short Rib Polydactyly Syndrome Type 1
Majewski Syndrome- Majewski Syndrome
- Short Rib-Polydactyly Syndrome, Type II
- Short Rib Polydactyly Syndrome, Type II
- Polydactyly With Neonatal Chondrodystrophy, Type II
- Short Rib-Polydactyly Syndrome, Majewski Type
- Short Rib Polydactyly Syndrome, Majewski Type
- Polydactyly with Neonatal Chondrodystrophy, Type 2
|
Below are MeSH descriptors whose meaning is more general than "Short Rib-Polydactyly Syndrome".
Below are MeSH descriptors whose meaning is more specific than "Short Rib-Polydactyly Syndrome".
This graph shows the total number of publications written about "Short Rib-Polydactyly Syndrome" by people in this website by year, and whether "Short Rib-Polydactyly Syndrome" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2018 | 0 | 1 | 1 |
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Below are the most recent publications written about "Short Rib-Polydactyly Syndrome" by people in Profiles.
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IFT52 as a Novel Candidate for Ciliopathies Involving Retinal Degeneration. Invest Ophthalmol Vis Sci. 2018 09 04; 59(11):4581-4589.