Carney-Stratakis syndrome
Carney-Stratakis syndrome is a recently described familial syndrome characterized by gastrointestinal stromal tumors (GIST) and paragangliomas, often at multiple sites
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Carney-Stratakis syndrome
Summary
Carney-Stratakis syndrome is a hereditary disorder[1].
Key Facts
- Carney-Stratakis syndrome's instance of is recorded as hereditary disorder[2].
- Carney-Stratakis syndrome's instance of is recorded as rare disease[3].
- Carney-Stratakis syndrome's instance of is recorded as class of disease[4].
- Carney-Stratakis syndrome is a type of gastrointestinal stromal tumor[5].
- Carney-Stratakis syndrome is a type of rare genetic endocrine disease[6].
- Carney-Stratakis syndrome is a type of multiple polyglandular tumor[7].
- Carney-Stratakis syndrome is a type of inherited tumor[8].
- Carney-Stratakis syndrome is a type of hereditary neoplastic syndromes[9].
- Carney-Stratakis syndrome is a type of syndrome[10].
- Carney-Stratakis syndrome is a type of autosomal dominant disease[11].
- Carney-Stratakis syndrome's NCI Thesaurus ID is recorded as C94831[12].
- Carney-Stratakis syndrome's different from is recorded as Carney's triad[13].
- Carney-Stratakis syndrome's genetic association is recorded as SDHB[14].
- Carney-Stratakis syndrome's genetic association is recorded as SDHD[15].
- Carney-Stratakis syndrome's genetic association is recorded as SDHC[16].
- Carney-Stratakis syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_97286[17].
- Carney-Stratakis syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080533[18].
- Carney-Stratakis syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0080533[19].
- Carney-Stratakis syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[20].