Monochromacy

Symptom Information:

Symptom ID: HPO:0007803
Synonyms:
Complete achromatopsia [HPO:0007803]
TOTAL COLORBLINDNESS [HPO:0007803]
Complete achromatopsia [OMIM:Complete achromatopsia]
Total colorblindness [OMIM:Total colorblindness]
Quality:
Cross references:
OMIM: "Complete achromatopsia" [OMIM:Complete achromatopsia]
OMIM: "Total colorblindness" [OMIM:Total colorblindness]
Is a (Direct Parents):
HPO         Abnormality of color vision
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:
Database Frequency: 3 / 7739
Resource:

All diseases associated with this symptom:

ACHROMATOPSIA 3 (OMIM:262300)
Jalili syndrome (Orphanet:1873)
Retinohepatoendocrinologic syndrome (Orphanet:3087)