Disease_Has_Molecular_Abnormality
Disease_May_Have_Associated_Disease
Disease_Mapped_To_Gene
CTRP Terminology
CTRP Disease Terminology
TP53 Gene Mutation
GDC Terminology
Comorbidity
Cellosaurus Disease Terminology
Risk Factor
TP53 Gene
EWS Authorized Value Terminology
EWS Medical History Table
Childhood Cancer Predisposition Study Terminology
CCPS Disease Terminology
GDC Value Terminology
OS Authorized Value Terminology
OS Medical History Table
HL Medical History Table
HL Authorized Value Terminology
Cellosaurus Terminology
Leukemia
Medulloblastoma
Hereditary Neoplastic Syndrome
Li-Fraumeni Syndrome
A rare, inherited predisposition to multiple cancers, caused by an alteration in the p53 tumor suppressor gene.
An autosomal dominant cancer predisposition syndrome caused by germline mutations of the TP53 gene. It is associated with breast carcinoma, choroid plexus carcinoma, adrenal cortex carcinoma, astrocytic tumors, medulloblastoma, soft tissue sarcoma, osteosarcoma, and leukemia.
C0085390
C3476
CCPS
CTRP
Cellosaurus
Disease or Syndrome
GDC
Li-Fraumeni
Li-Fraumeni Familial Cancer Susceptibility Syndrome
Li-Fraumeni Syndrome
Li-Fraumeni Syndrome
Li-Fraumeni Syndrome
Li-Fraumeni Syndrome
Li-Fraumeni Syndrome, TP53-Associated
Li-Fraumeni syndrome
Li-Fraumeni_Syndrome
PCDC
TP53-Associated Li-Fraumeni Syndrome
Choroid Plexus Carcinoma
Breast Carcinoma
Medical History Reported Term
Osteosarcoma
Soft Tissue Sarcoma
Adrenal Cortical Carcinoma