loading...| Preferred Name |
Choroid plexus carcinoma |
| ID |
http://www.orpha.net/ORDO/Orphanet_251899 |
| definition |
Choroid plexus carcinoma is a rare and highly aggressive malignant type of choroid plexus tumor (see this term) occurring almost exclusively in children, presenting with cerebrospinal fluid obstruction in the lateral ventricles (most common), the fourth and third ventricles or in multiple ventricles, leading to hydrocephalus and increased intracranial pressure, and manifesting with nausea, vomiting, abnormal eye movements, gait impairment, seizures and enlarged head circumference. |
| definition_citation |
Orphanet |
| expertlink |
https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=251899 |
| has_age_of_onset |
Childhood |
| has_inheritance |
Autosomal dominant |
| hasDbXref |
MedDRA:10067478 ICD-11:2A00.22 ICD-10:C71.7 OMIM:260500 UMLS:C0431109 |
| label |
Choroid plexus carcinoma |
| notation |
ORPHA:251899 |
| part_of | |
| prefixIRI |
ORDO:Orphanet_251899 |
| prefLabel |
Choroid plexus carcinoma |
| present_in |
Europe AND has_lifetime_prevalence_average_value : 0.35 AND has_lifetime_prevalence_range : 1-9 / 1 000 000 Europe AND has_annual_incidence_average_value : 0.01 AND has_annual_incidence_range : <1 / 1 000 000 Europe AND has_point_prevalence_range : 1-9 / 1 000 000 |
| treeView | |
| subClassOf |