loading...| Preferred Name |
Congenital hydrocephalus |
| ID |
http://www.orpha.net/ORDO/Orphanet_2185 |
| definition |
A rare central nervous system malformation characterized by abnormally enlarged cerebral ventricles due to impaired cerebrospinal fluid circulation. It arises in utero and can be either acquired or inherited. The severity of the resulting brain damage depends on the duration and extent of ventriculomegaly. |
| definition_citation |
Orphanet |
| expertlink |
https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2185 |
| has_age_of_onset |
Antenatal |
| has_inheritance |
Not applicable |
| hasDbXref |
ICD-10:Q03.9 ICD-10:Q03.1 OMIM:236600 ICD-10:Q03.0 UMLS:C0020256 OMIM:615219 MedDRA:10010506 ICD-11:LA04 ICD-10:Q03.8 |
| label |
Congenital hydrocephalus |
| notation |
ORPHA:2185 |
| part_of | |
| prefixIRI |
ORDO:Orphanet_2185 |
| prefLabel |
Congenital hydrocephalus |
| present_in |
Worldwide AND has_point_prevalence_range : Unknown Europe AND has_birth_prevalence_average_value : 46.5 AND has_birth_prevalence_range : 1-5 / 10 000 United States AND has_birth_prevalence_average_value : 59.0 AND has_birth_prevalence_range : 6-9 / 10 000 |
| treeView | |
| subClassOf |