Tritanomaly
Symptom Information:
Symptom ID: | HPO:0000552 | ||||||
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) Anomalous trichromacy(HPO:0011519) Tritanomaly(HPO:0000552) MedDRA: |
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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) |