Preferred Label : Papilloma of choroid plexus;
Symbol : CPP;
CISMeF acronym : CPC; CPP;
Type : Phenotype, molecular basis known;
Alternative titles and symbols : Choroid plexus papilloma;
Included titles and symbols : Choroid plexus carcinoma; CPC;
Description : Choroid plexus tumors are of neuroectodermal origin and range from benign choroid
plexus papillomas (CPPs) to malignant choroid carcinomas (CPCs). These rare tumors
generally occur in childhood, but have also been reported in adults. Patients typically
present with signs and symptoms of increased intracranial pressure including headache,
hydrocephalus, papilledema, nausea, vomiting, cranial nerve deficits, gait impairment,
and seizures (summary by Safaee et al., 2013).;
Inheritance : Autosomal dominant;
Molecular basis : Caused by mutation in the tumor protein p53 gene (TP53, 191170.0036);
Neoplasia : Malignant transformation of choroid plexus papilloma;
Prefixed ID : #260500;
Origin ID : 260500;
UMLS CUI : C0205770;
Automatic exact mappings (from CISMeF team)
Currated CISMeF NLP mapping
DO Cross reference
False automatic mappings
Genes related to phenotype
HPO term(s)
ORDO concept(s)
See also inter- (CISMeF)
Semantic type(s)
UMLS correspondences (same concept)
Validated automatic mappings to BTNT
Validated automatic mappings to NTBT