Monochromacy
Symptom Information:
Symptom ID: | HPO:0007803 | ||||
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) Monochromacy(HPO:0007803) MedDRA: |
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Database Frequency: | 3 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
ACHROMATOPSIA 3 | (OMIM:262300) |
Jalili syndrome | (Orphanet:1873) |
Retinohepatoendocrinologic syndrome | (Orphanet:3087) |