Optic neuropathy
Symptom Information:
Symptom ID: | HPO:0001138 | ||||
Synonyms: |
|
||||
Quality: | |||||
Cross references: |
|
||||
Is a (Direct Parents): |
|
||||
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) Optic neuropathy(HPO:0001138) MedDRA: Eye disorders(MedDRA:10015919) Vision disorders(MedDRA:10047518) Visual pathway disorders(MedDRA:10047573) Optic neuropathy(HPO:0001138) |
||||
Database Frequency: | 12 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
CADASIL | (Orphanet:136) |
Cherubism | (Orphanet:184) |
LEUKOENCEPHALOPATHY WITH ATAXIA | (OMIM:615651) |
Leber hereditary optic neuropathy | (Orphanet:104) |
Leber plus disease | (Orphanet:99718) |
Polyarteritis nodosa, childhood-onset | (OMIM:615688) |
Primary hyperoxaluria | (Orphanet:416) |
Primary hyperoxaluria type 1 | (Orphanet:93598) |
Sarcoidosis | (Orphanet:797) |
Wolfram syndrome 2 | (OMIM:604928) |
X-linked Charcot-Marie-Tooth disease type 5 | (Orphanet:99014) |
[DEL] LEBER OPTIC ATROPHY | (OMIM:535000) |