MSeqDR Mitochondrial Disease Portal


 
*:HP: HPO terms, ND: NAMDC terms.
  Most Studied  CPEO, Complex I Deficiency, COXPD1, Leigh, LHON, MELAS, MERRF, NARP, SANDO
Disease Browser
Parent Node:
expandbrain disease (MONDO:0005560)
Parent Node:
expandhypertensive disorder (MONDO:0005044)
Parent Node:
expandneurovascular disease (MONDO:0043218)
..Starting node
..expandintracranial hypertension ()

       Child Nodes:
........expandhypertensive encephalopathy ()
........expandpseudotumor cerebri ()



 Sister Nodes: 
..expandataxia - telangiectasia-like disorder ()
..expandataxia telangiectasia ()
..expandBannayan-Riley-Ruvalcaba syndrome ()
..expandbasal laminar drusen ()
..expandbenign choroid plexus neoplasm ()
..expandbenign neoplasm of choroid ()
..expandcampomelia, Cumming type ()
..expandcarotid body paraganglioma ()
..expandcavernous sinus meningioma ()
..expandcentral areolar choroidal dystrophy ()
..expandcentral nervous system angiosarcoma ()
..expandcentral nervous system hemangioma ()
..expandcentral nervous system vasculitis ()
..expandcerebral sinovenous thrombosis ()
..expandcerebral visual impairment ()
..expandcerebrovascular disorder ()
..expandChar syndrome ()
..expandchoroid cancer ()
..expandchoroid plexus cancer ()
..expandchoroidal sclerosis ()
..expandchoroideremia ()
..expandCryoglobulinemic vasculitis ()
..expanddeafness-lymphedema-leukemia syndrome ()
..expandeosinophilic granulomatosis with polyangiitis ()
..expanderythromelalgia ()
..expandeyelid capillary hemangioma ()
..expandFabry disease ()
..expandgenetic central nervous system and retinal vascular disease ()
..expandgyrate atrophy ()
..expandhemangioblastoma ()
..expandhemangioma of retina ()
..expandHennekam syndrome ()
..expandhypercoagulability syndrome due to glycosylphosphatidylinositol deficiency ()
..expandintracranial hypertension ()
..expandjugulotympanic paraganglioma ()
..expandmacrothrombocytopenia-lymphedema-developmental delay-facial dysmorphism-camptodactyly syndrome ()
..expandmedian arcuate ligament syndrome ()
..expandMeige disease ()
..expandmicrocephaly with or without chorioretinopathy, lymphedema, or mental retardation ()
..expandmicrocephaly-capillary malformation syndrome ()
..expandmicroscopic polyangiitis ()
..expandmigraine disorder ()
..expandneoplasm of aortic body ()
..expandneurofibromatosis type 1 ()
..expandNorman-Roberts syndrome ()
..expandparagangliomas 1 ()
..expandparagangliomas 2 ()
..expandparagangliomas 3 ()
..expandparagangliomas 4 ()
..expandparagangliomas 5 ()
..expandPEHO syndrome ()
..expandpelvis syndrome ()
..expandpolyarteritis nodosa ()
..expandprolidase deficiency ()
..expandProteus syndrome ()
..expandretinal dystrophies primarily involving Bruch's membrane ()
..expandretinal ischemia ()
..expandretinal vascular disease ()
..expandsimple cryoglobulinemia ()
..expandsporadic pheochromocytoma/secreting paraganglioma ()
..expandSturge-Weber syndrome ()
..expandsubarachnoid hemorrhage (disease) ()
..expandtrigeminal autonomic cephalalgia ()
..expandWilliams syndrome ()
..expandWyburn-Mason syndrome ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:6810
Name:intracranial hypertension
Definition:A finding characterized by increased cerebrospinal fluid pressure within the skull.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:raised intracranial pressure
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal