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Start free with EleplanHereditary leiomyomatosis and renal cell cancer
ORPHA:523Disease
Also called Familial leiomyomatosis and renal cell cancer · Familial leiomyomatosis cutis et uteri · Familial leiomyomatosis with renal carcinoma · Familial multiple cutaneous leiomyomas · HLRCC · Hereditary leiomyomatosis · Hereditary leiomyomatosis with renal carcinoma · Hereditary multiple cutaneous leiomyomas · MCUL · Multiple cutaneous and uterine leiomyomas · Reed syndrome
What it is
Hereditary leiomyomatosis and renal cell cancer (HLRCC) is a hereditary cancer syndrome characterized by a predisposition to cutaneous and uterine leiomyomas and, in some families, to renal cell cancer.
Key facts
- Age of onset
- Adolescent, Adult, Elderly
- Inheritance
- Autosomal dominant
- Classified as
- Disease
Signs and symptoms
These ranges are how often a sign appears across everyone diagnosed, not a prediction for one person — most people have some of these and not others. Orphanet also records findings that are specifically absent in this disease; those are in the data but not listed here.
Gene
ICD-10 codes
ICD-10 has no distinct code for most rare diseases, so many are filed under the nearest available one. A shared code identifies the group, not this disease — the ORPHAcode above is what identifies it.
Related health topics
Reached through the ICD-10 categories this disease is filed under, so these describe the broader group rather than this disease specifically.
Cross-references
Orphadata Science: Free access data from Orphanet. © INSERM 1999. Data version 2026-06-23. Available under CC BY 4.0. This is a reference, not medical advice.
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