Papilledema
Symptom Information:
Symptom ID: | HPO:0001085 | ||||||||||||||||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) |
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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) |