Central scotoma

Symptom Information:

Symptom ID: HPO:0000603
Synonyms:
Central scotomata [HPO:0000603]
Central scotoma [OMIM:Central scotoma]
Central scotomata [OMIM:Central scotomata]
Central scotoma (in some patients) [OMIM:Central scotoma (in some patients)]
Quality:
Cross references:
OMIM: "Central scotoma" [OMIM:Central scotoma]
OMIM: "Central scotomata" [OMIM:Central scotomata]
OMIM: "Central scotoma (in some patients)" [OMIM:Central scotoma (in some patients)]
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)
                      Central scotoma(HPO:0000603)
MedDRA:
Database Frequency: 18 / 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)
Autosomal recessive optic atrophy, OPA7 type (Orphanet:227976)
Autosomal recessive spastic paraplegia type 55 (Orphanet:320375)
CONE-ROD DYSTROPHY 17 (OMIM:615163)
CONE-ROD DYSTROPHY 18 (OMIM:615374)
CONE-ROD DYSTROPHY 3 (OMIM:604116)
CONE-ROD DYSTROPHY, X-LINKED, 3 (OMIM:300476)
Hereditary motor and sensory neuropathy type 6 (Orphanet:90120)
Leber hereditary optic neuropathy (Orphanet:104)
MACULAR DYSTROPHY, VITELLIFORM, 5 (OMIM:616152)
Mohr-Tranebjaerg syndrome (Orphanet:52368)
Necrotizing encephalomyelopathy, subacute, of Leigh, adult (OMIM:161700)
OPTIC ATROPHY 1 (OMIM:165500)
OPTIC ATROPHY 5 (OMIM:610708)
RETINITIS PIGMENTOSA 66 (OMIM:615233)
Retinal macular dystrophy type 2 (Orphanet:319640)
[DEL] LEBER OPTIC ATROPHY (OMIM:535000)