Hemeralopia
Symptom Information:
Symptom ID: | HPO:0012047 | ||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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 loss(HPO:0000572) Hemeralopia(HPO:0012047) Visual disorders NEC(MedDRA:10047541) 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) |
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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) |