MeSH Browser

MeSH Supplementary: Hereditary leiomyomatosis and renal cell cancer
Unique ID: C535516
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C535516
Entry Term(s): Cutaneous leiomyomata with uterine leiomyomata; Leiomyoma, hereditary multiple, of skin; Leiomyoma, multiple cutaneous; Leiomyomatosis and renal cell cancer, hereditary; Multiple cutaneous and uterine leiomyomata 1; Multiple cutaneous and uterine leiomyomatosis; Reed's syndrome
Registry Numbers: 0
Heading Mapped to: *Neoplastic Syndromes, Hereditary; *Skin Neoplasms; *Uterine Neoplasms; *Leiomyomatosis
Frequency: 173
Note: A hereditary condition where patients present with cutaneous LEIOMYOMAS (female patients may also have uterine leiomyomas) and are at increased risk for developing KIDNEY NEOPLASMS. Tumors initally appear during adulthood on the skin of the torso, arms, legs, and face and increase in size and number over time; 10% to 16% of patients develop RENAL CELL CARCINOMA. A heterozygous germline mutation in the FH gene has been identified. OMIM: 150800
Date of Entry: 2010/08/25
Revision Date: 2017/04/19

Hereditary leiomyomatosis and renal cell cancer MeSH Supplementary Concept Data 2025