Tritanomaly

Symptom Information:

Symptom ID: HPO:0000552
Synonyms:
Blue-yellow dyschromatopsia [HPO:0000552]
BLUE/YELLOW COLOR VISION DEFECT [HPO:0000552]
Dyschromatopsia, blue-yellow [HPO:0000552]
Blue-yellow dyschromatopsia [OMIM:Blue-yellow dyschromatopsia]
Blue/yellow color vision defect [OMIM:Blue/yellow color vision defect]
Dyschromatopsia, blue-yellow [OMIM:Dyschromatopsia, blue-yellow]
Quality:
Cross references:
OMIM: "Blue-yellow dyschromatopsia" [OMIM:Blue-yellow dyschromatopsia]
OMIM: "Blue/yellow color vision defect" [OMIM:Blue/yellow color vision defect]
OMIM: "Dyschromatopsia, blue-yellow" [OMIM:Dyschromatopsia, blue-yellow]
Is a (Direct Parents):
HPO         Anomalous trichromacy
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)
                      Anomalous trichromacy(HPO:0011519)
                         Tritanomaly(HPO:0000552)
MedDRA:
Database Frequency: 6 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant optic atrophy and congenital deafness (Orphanet:3212)
Autosomal dominant optic atrophy, classic type (Orphanet:98673)
OPTIC ATROPHY 1 (OMIM:165500)
OPTIC ATROPHY 5 (OMIM:610708)
RETINITIS PIGMENTOSA 37 (OMIM:611131)
Tritanopia (Orphanet:88629)