Protanomaly
Symptom Information:
Symptom ID: | HPO:0200018 | ||||
Synonyms: |
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Quality: | |||||
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) Abnormality of color vision(HPO:0000551) Dyschromatopsia(HPO:0007641) Red-green dyschromatopsia(HPO:0000642) Protanomaly(HPO:0200018) Anomalous trichromacy(HPO:0011519) Protanomaly(HPO:0200018) MedDRA: |
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Database Frequency: | 1 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
COLORBLINDNESS, PARTIAL, PROTAN SERIES | (OMIM:303900) |