Hemeralopia

Symptom Information:

Symptom ID: HPO:0012047
Synonyms:
Day blindness (disorder) [Orphanet:5510]
Hemeralopia [Orphanet:5510]
Hemeralopia [OMIM:Hemeralopia]
Night blindness/hemeralopia [Orphanet:5510]
Blindness day [Orphanet:5510]
Blindness day [MedDRA:10005178]
Hemeralopia [MedDRA:10005178]
Day blindness [OMIM:Day blindness]
Quality:
Cross references:
Orphanet:5510 "Night blindness/hemeralopia" [Orphanet:5510]
OMIM: "Hemeralopia" [OMIM:Hemeralopia]
OMIM: "Day blindness" [OMIM:Day blindness]
UMLS:C0018975 "Hemeralopia" [Orphanet:5510]
Is a (Direct Parents):
HPO         Abnormality of vision
Orphanet Abnormality of the eye
MedDRA Visual loss
Orphanet Nyctalopia
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)
                Hemeralopia(HPO:0012047)
MedDRA:
Eye disorders(MedDRA:10015919)
    Vision disorders(MedDRA:10047518)
       Visual disorders NEC(MedDRA:10047541)
          Visual loss(HPO:0000572)
             Hemeralopia(HPO:0012047)
       Visual loss(HPO:0000572)
             Hemeralopia(HPO:0012047)
Nervous system disorders(MedDRA:10029205)
    Neurological disorders of the eye(MedDRA:10029301)
       Neurologic visual problems NEC(MedDRA:10029292)
          Visual loss(HPO:0000572)
             Hemeralopia(HPO:0012047)
Database Frequency: 7 / 7739
Resource:

All diseases associated with this symptom:

ACHROMATOPSIA 2 (OMIM:216900)
Achromatopsia (Orphanet:49382)
Goldmann-Favre syndrome (Orphanet:53540)
MELAS (Orphanet:550)
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1A (OMIM:310500)
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B (OMIM:257270)
Oguchi disease (Orphanet:75382)