Papilledema

Symptom Information:

Symptom ID: HPO:0001085
Synonyms:
Optic papillitis (disorder) [Orphanet:5390]
Optic disc swelling (finding) [Orphanet:5390]
Optic disc edema (disorder) [Orphanet:5390]
Papilledema [Orphanet:5390]
Papilledema [OMIM:Papilledema]
Optic nerve anomaly/optic atrophy/anomaly of the papilla [Orphanet:5390]
Papillitis [Orphanet:5390]
Papilloedema [Orphanet:5390]
Optic discs blurred [Orphanet:5390]
Papillitis [MedDRA:10033708]
Papillitis NOS [MedDRA:10033708]
Papilloedema [MedDRA:10033712]
Disc congestion in ocular fundus [MedDRA:10033712]
Disc oedema in ocular fundus [MedDRA:10033712]
Disc redness in ocular fundus [MedDRA:10033712]
Optic disc engorgement [MedDRA:10033712]
Optic disc opacity [MedDRA:10033712]
Optic nerve congestion [MedDRA:10033712]
Optic nerve edema [MedDRA:10033712]
Optic nerve oedema [MedDRA:10033712]
Papilledema [MedDRA:10033712]
Papilledema associated with decreased ocular pressure [MedDRA:10033712]
Papilledema associated with increased intracranial pressure [MedDRA:10033712]
Papilledema associated with retinal disorder [MedDRA:10033712]
Papilledema, unspecified [MedDRA:10033712]
Disc edema in ocular fundus [MedDRA:10033712]
Papilloedema associated with decreased ocular pressure [MedDRA:10033712]
Papilloedema associated with increased intracranial pressure [MedDRA:10033712]
Papilloedema associated with retinal disorder [MedDRA:10033712]
Papilloedema, unspecified [MedDRA:10033712]
Optic discs blurred [MedDRA:10030923]
Optic disc edema [OMIM:Optic disc edema]
Quality:
Cross references:
Orphanet:5390 "Optic nerve anomaly/optic atrophy/anomaly of the papilla" [Orphanet:5390]
OMIM: "Papilledema" [OMIM:Papilledema]
OMIM: "Optic disc edema" [OMIM:Optic disc edema]
UMLS:C0155288 "Papilledema" [HPO:0001085]
UMLS:C0030353 "Papilledema" [Orphanet:5390]
Is a (Direct Parents):
Orphanet Optic atrophy
MedDRA Ocular signs and symptoms NEC
Orphanet Abnormality of the eye
MedDRA Increased intracranial pressure disorders
HPO         Abnormality of the optic nerve
MedDRA Inflammations
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the eye(HPO:0000478)
          Abnormal eye morphology(HPO:0012372)
             Abnormality of the globe(HPO:0012374)
                Abnormality of the posterior segment of the globe(HPO:0004329)
                   Abnormality of the fundus(HPO:0001098)
                      Abnormality of the optic nerve(HPO:0000587)
                         Papilledema(HPO:0001085)
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Increased intracranial pressure and hydrocephalus(MedDRA:10021666)
       Increased intracranial pressure disorders(MedDRA:10062912)
          Papilledema(HPO:0001085)
    Neurological disorders of the eye(MedDRA:10029301)
       Ocular signs and symptoms NEC(MedDRA:10030952)
          Papilledema(HPO:0001085)
General disorders and administration site conditions(MedDRA:10018065)
    General system disorders NEC(MedDRA:10018073)
       Inflammations(MedDRA:10021950)
          Papilledema(HPO:0001085)
Database Frequency: 31 / 7739
Resource:

All diseases associated with this symptom:

ARTERITIS, FAMILIAL GRANULOMATOUS, WITH JUVENILE POLYARTHRITIS (OMIM:108050)
Autosomal dominant Kenny-Caffey syndrome (Orphanet:93325)
Blau syndrome (Orphanet:90340)
Blue diaper syndrome (Orphanet:94086)
COMPLEX I, SUBUNIT ND2 (OMIM:516001)
COMPLEX I, SUBUNIT ND5 (OMIM:516005)
COMPLEX I, SUBUNIT ND6 (OMIM:516006)
COMPLEX IV, CYTOCHROME c OXIDASE SUBUNIT I (OMIM:516030)
CRANIODIAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT (OMIM:122860)
CYTOCHROME b OF COMPLEX III (OMIM:516020)
CYTOCHROME c OXIDASE III (OMIM:516050)
Craniodiaphyseal dysplasia (Orphanet:1513)
Craniosynostosis and dental anomalies (Orphanet:284149)
DEAFNESS, SENSORINEURAL, WITH PERIPHERAL NEUROPATHY AND ARTERIAL DISEASE (OMIM:124950)
HYPERVITAMINOSIS A, SUSCEPTIBILITY TO (OMIM:240150)
Hurler-Scheie syndrome (Orphanet:93476)
Idiopathic intracranial hypertension (Orphanet:238624)
Infantile onset spinocerebellar ataxia (Orphanet:1186)
Kenny-Caffey syndrome (Orphanet:2333)
Leber hereditary optic neuropathy (Orphanet:104)
Leber plus disease (Orphanet:99718)
Leigh syndrome (Orphanet:506)
Lymphangioleiomyomatosis (Orphanet:538)
MELAS (Orphanet:550)
MERRF (Orphanet:551)
Mucopolysaccharidosis type 2 (Orphanet:580)
Mucopolysaccharidosis type 2, attenuated form (Orphanet:217093)
Nasal dermoid cyst (Orphanet:141103)
Permanent neonatal diabetes mellitus - pancreatic and cerebellar agenesis (Orphanet:65288)
Thiamine-responsive megaloblastic anemia syndrome (Orphanet:49827)
Wolfram syndrome (Orphanet:3463)