LFS1

Introduction: LFS1

Description of LFS1

LFS1 (medical condition): A rare inherited disorder characterized by tumor development by young...more »

See also:

Li-Fraumeni syndrome:
  »Introduction: Li-Fraumeni syndrome
  »Symptoms of Li-Fraumeni syndrome

LFS1: Rare Disease

Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

LFS1 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that LFS1, or a subtype of LFS1, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

LFS1 as a Disease

LFS1: Another name for Li-Fraumeni syndrome (or close medical condition association).
  »Introduction: Li-Fraumeni syndrome
  »Symptoms of Li-Fraumeni syndrome

LFS1: Related Diseases

LFS1: LFS1 is listed as a type of (or associated with) the following medical conditions in our database:

• Genetic conditions
• Benign tumors
• Soft tissue tumors
• Cancer

Symptoms of LFS1 (Li-Fraumeni syndrome)

Some of the symptoms of LFS1 incude:

• Breast cancer
• Soft tissue sarcoma
• Brain tumor
• Osteosarcoma
• Leukemia

See full list of 14 symptoms of LFS1 (Li-Fraumeni syndrome)

LFS1: Related Disease Topics

These medical disease topics may be related to LFS1:

• autosomal dominant disorder
• breast cancer
• sarcoma
• bone sarcoma
• leukemia
• p53 tumour suppressor gene

Terms associated with LFS1:

Terms Similar to LFS1:

• SBLA syndrome
• Sarcoma family syndrome of Li and Fraumeni
• Li Fraumeni syndrome

Source - NIH

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