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Results: 7

1.

Fibromatosis

A poorly circumscribed neoplasm arising from the soft tissues. It is characterized by the presence of spindle-shaped fibroblasts and an infiltrative growth pattern. [from NCI]

MedGen UID:
8836
Concept ID:
C0016048
Neoplastic Process
2.

Spondylometaepiphyseal dysplasia short limb-hand type

MedGen UID:
338595
Concept ID:
C1849011
Disease or Syndrome
3.

Desmoid disease, hereditary

Hereditary desmoid disease usually presents as an extraintestinal manifestation of familial adenomatous polyposis (FAP; 175100), also known as Gardner syndrome, which is an autosomal dominant disorder caused by germline mutation in the APC gene. The desmoid tumors are usually intraabdominal and, although benign, can be locally aggressive and result in significant morbidity. Desmoid tumors can also arise sporadically (Couture et al., 2000). [from OMIM]

MedGen UID:
338210
Concept ID:
C1851124
Disease or Syndrome
4.

Fibromatosis, Aggressive

A childhood counterpart of abdominal or extra-abdominal desmoid tumors, characterized by firm subcutaneous nodules that grow rapidly in any part of the body but do not metastasize. The adult form of abdominal fibromatosis is FIBROMATOSIS, ABDOMINAL. (Stedman, 25th ed) [from MeSH]

MedGen UID:
38187
Concept ID:
C0079218
Neoplastic Process
5.

Zonal necrosis

A morphologic finding referring to the presence of necrosis that is confined to a specific anatomic zone. Representative example is the hepatic zonal necrosis that affects the hepatic parenchyma either in the portal areas or around the hepatic veins. [from NCI]

MedGen UID:
473045
Concept ID:
C0333514
Pathologic Function
6.

Nuclear Atypia

MedGen UID:
233787
Concept ID:
C1335070
Finding
7.

Cytologic atypia

MedGen UID:
90720
Concept ID:
C0333865
Cell or Molecular Dysfunction

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