Severe visual impairment

Symptom Information:

Symptom ID: HPO:0001141
Synonyms:
Marked vision impairment [HPO:0001141]
Severely impaired vision [HPO:0001141]
Marked vision impairment [OMIM:Marked vision impairment]
Severe visual impairment [OMIM:Severe visual impairment]
Severely impaired vision [OMIM:Severely impaired vision]
Quality:
Cross references:
OMIM: "Marked vision impairment" [OMIM:Marked vision impairment]
OMIM: "Severe visual impairment" [OMIM:Severe visual impairment]
OMIM: "Severely impaired vision" [OMIM:Severely impaired vision]
Is a (Direct Parents):
HPO         Visual impairment
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 impairment(HPO:0000505)
                   Severe visual impairment(HPO:0001141)
MedDRA:
Database Frequency: 11 / 7739
Resource:

All diseases associated with this symptom:

ACHROMATOPSIA 3 (OMIM:262300)
ALG3-CDG (Orphanet:79321)
Bardet-Biedl syndrome 3 (OMIM:600151)
CATARACT 40 (OMIM:302200)
Corneal-cerebellar syndrome (Orphanet:3177)
Hermansky-Pudlak syndrome with pulmonary fibrosis (Orphanet:231500)
Leber congenital amaurosis 6 (OMIM:613826)
RETINITIS PIGMENTOSA 58 (OMIM:613617)
Senior-Loken syndrome 4 (OMIM:606996)
Severe X-linked intellectual deficit, Gustavson type (Orphanet:3078)
Åland Islands eye disease (Orphanet:178333)