| Metadata | |
|---|---|
| ID | DOID:0050430 |
| Name | multiple endocrine neoplasia type 2A |
| Definition | A multiple endocrine neoplasia characterized by medullary carcinoma of the thyroid, pheochromocytoma, hyperparathyroidism, and occasionally cutaneous lichen amyloidosis. https://www.ncbi.nlm.nih.gov/pubmed/15965261, http://ghr.nlm.nih.gov/condition/multiple-endocrine-neoplasia, http://www.merckmanuals.com/professional/endocrine_and_metabolic_disorders/multiple_endocrine_neoplasia_men_syndromes/multiple_endocrine_neoplasia_type_2a_men_2a.html, https://www.rarediseases.org/rare-disease-information/rare-diseases/byID/1244/viewAbstract |
| Xrefs |
SNOMEDCT_US_2023_03_01:721188000 |
| Subsets |
DO_FlyBase_slim DO_rare_slim NCIthesaurus |
| Synonyms |
MEN2A [EXACT] multiple endocrine neoplasia II [EXACT] Sipple syndrome [EXACT] |
| Parent Relationships | |
| Subclass Logical Relationships |
has material basis in some autosomal dominant inheritance |