Centrocecal scotoma

Symptom Information:

Symptom ID: HPO:0000576
Synonyms:
Centrocecal scotoma [OMIM:Centrocecal scotoma]
Centrocecal scotoma (acute phase) [OMIM:Centrocecal scotoma (acute phase)]
Quality:
Cross references:
OMIM: "Centrocecal scotoma" [OMIM:Centrocecal scotoma]
OMIM: "Centrocecal scotoma (acute phase)" [OMIM:Centrocecal scotoma (acute phase)]
Is a (Direct Parents):
HPO         Scotoma
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the eye(HPO:0000478)
          Abnormal eye physiology(HPO:0012373)
             Abnormality of vision(HPO:0000504)
                Visual field defect(HPO:0001123)
                   Scotoma(HPO:0000575)
                      Centrocecal scotoma(HPO:0000576)
MedDRA:
Database Frequency: 6 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant optic atrophy and congenital deafness (Orphanet:3212)
Autosomal dominant optic atrophy, classic type (Orphanet:98673)
Leber hereditary optic neuropathy (Orphanet:104)
Leber plus disease (Orphanet:99718)
OPTIC ATROPHY 1 (OMIM:165500)
[DEL] LEBER OPTIC ATROPHY (OMIM:535000)