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Items: 7

1.

Familial multiple lipomatosis

Familial multiple lipomatosis (FML) is a rare autosomal dominant disorder characterized by numerous encapsulated lipomas on the trunk and extremities (Keskin et al., 2002). [from OMIM]

MedGen UID:
698553
Concept ID:
C1275273
Disease or Syndrome
2.

Congenital laryngeal adductor palsy

MedGen UID:
140759
Concept ID:
C0396060
Disease or Syndrome
3.

Hibernoma

A rare benign slow growing adipose tissue tumor, characterized by the presence of polygonal brown fat cells with multivacuolated and/or granular cytoplasm. The tumor is usually painless and is most often seen in young adults. [from NCI]

MedGen UID:
61456
Concept ID:
C0205822
Neoplastic Process
4.

Pleomorphic lipoma

A benign circumscribed tumor characterized by small spindle cells, rounded hyperchromatic cells and multinucleated giant cells with radially arranged nuclei. [from NCI]

MedGen UID:
60027
Concept ID:
C0205823
Neoplastic Process
5.

Palmoplantar pustulosis

A chronic, relapsing, pustular eruption that is localized to the palms and soles. [from HPO]

MedGen UID:
45290
Concept ID:
C0030246
Disease or Syndrome
6.

Lipoma

Benign neoplasia derived from lipoblasts or lipocytes of white or brown fat. May be angiomatous or hibernomatous. [from HPO]

MedGen UID:
44173
Concept ID:
C0023798
Neoplastic Process
7.

Lichen planopilaris

A rare cutaneous variant of lichen planus which affects hair follicles. It may occur on its own or in association with more common forms of lichen planus, usually classical type and/or oral lichen planus. [from ORDO]

MedGen UID:
44150
Concept ID:
C0023645
Disease or Syndrome
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