| Metadata | |
|---|---|
| ID | DOID:13482 |
| PURL | http://purl.obolibrary.org/obo/DOID_13482 Copy |
| Name | Proteus syndrome |
| Definition | A syndrome characterized by highly variable, progressive features including asymmetric and disproportionate overgrowth of body parts, connective tissue nevi, epidermal nevi, dysregulated adipose tissue, vascular malformations, dysmorphic facies with seizures or intellectual disability, and tumors that has_material_basis_in mosaicism for a somatic activating mutation in the AKT1 gene on chromosome 14q32.3. There is significant risk of deep vein thrombosis. https://ghr.nlm.nih.gov/condition/proteus-syndrome, https://www.ncbi.nlm.nih.gov/books/NBK99495/, https://pubmed.ncbi.nlm.nih.gov/23992099/ |
| Xrefs |
SNOMEDCT_US_2025_09_01:394527003 |
| SKOS |
exactMatch MESH:D016715 exactMatch UMLS_CUI:C0085261 exactMatch MIM:176920 exactMatch NCI:C85032 exactMatch GARD:7475 exactMatch ORDO:744 |
| Subsets |
DO_rare_slim NCIthesaurus |
| Synonyms |
Wiedemann's syndrome [RELATED] |
| Parent Relationships |
is_a syndrome |