"Costello 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.
Rare congenital disorder with multiple anomalies including: characteristic dysmorphic craniofacial features, musculoskeletal abnormalities, neurocognitive delay, and high prevalence of cancer. Germline mutations in H-Ras protein can cause Costello syndrome. Costello syndrome shows early phenotypic overlap with other disorders that involve MAP KINASE SIGNALING SYSTEM (e.g., NOONAN SYNDROME and cardiofaciocutaneous syndrome).
| Descriptor ID |
D056685
|
| MeSH Number(s) |
C05.660.207.219 C16.131.077.256 C16.320.185
|
| Concept/Terms |
Costello Syndrome- Costello Syndrome
- Syndrome, Costello
- Faciocutaneoskeletal Syndrome
- Faciocutaneoskeletal Syndromes
- Syndrome, Faciocutaneoskeletal
- Syndromes, Faciocutaneoskeletal
- FCS Syndrome
- FCS Syndromes
- Syndrome, FCS
- Syndromes, FCS
|
Below are MeSH descriptors whose meaning is more general than "Costello Syndrome".
Below are MeSH descriptors whose meaning is more specific than "Costello Syndrome".
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Below are the most recent publications written about "Costello Syndrome" by people in Profiles.
MeSH information
