Optic neuropathy

Symptom Information:

Symptom ID: HPO:0001138
Synonyms:
Optic neuropathy [OMIM:Optic neuropathy]
Optic neuropathy [MedDRA:10061323]
Quality:
Cross references:
OMIM: "Optic neuropathy" [OMIM:Optic neuropathy]
Is a (Direct Parents):
MedDRA Visual pathway disorders
HPO         Abnormality of the optic nerve
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)