liver mesenchymal hamartoma
A multicystic, tumor-like hamartomatous lesion that arises from the liver during fetal development. Clinically, it usually presents as an abdominal mass associated with abdominal distention. Following resection, the prognosis is usually good. [ NCIT:C5751 ]
Term info
- SCTID:715397000 (MONDO:equivalentTo)
- UMLS:C1333971 (NCIT:C5751)
- Orphanet:386 (MONDO:equivalentTo)
- NCIT:C5751 (MONDO:equivalentTo)
- GARD:0002651 (MONDO:equivalentTo)
- UMLS:C0334091 (Orphanet:386)
gard_rare, ordo_disease
Editor note: in NCIT this is classified as non-neoplastic
A multicystic, tumor-like hamartomatous lesion that arises from the liver during fetal development. Clinically, it usually presents as an abdominal mass associated with abdominal distention. Following resection, the prognosis is usually good.
http://linkedlifedata.com/resource/umls/id/C1333971, http://purl.obolibrary.org/obo/NCIT_C5751, http://identifiers.org/snomedct/715397000, http://purl.obolibrary.org/obo/Orphanet_386, http://linkedlifedata.com/resource/umls/id/C0334091
http://purl.obolibrary.org/obo/MONDO_0017632
MHL, liver mesenchymal hamartoma, mesenchymal hamartoma of the liver, hepatic mesenchymal hamartoma, liver MH, biliary hamartoma, VMC, Von Meyenburg complexes disease, mesenchymal hamartoma of liver
hepatic cystic hamartoma
MONDO:0018308
https://rarediseases.info.nih.gov/diseases/2651/hepatic-cystic-hamartoma