Dyschromatopsia
Symptom Information:
Symptom ID: | HPO:0007641 | |||||||||||||||||||||||||||||||||||||||||
Synonyms: |
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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) MedDRA: Eye disorders(MedDRA:10015919) Vision disorders(MedDRA:10047518) Dyschromatopsia(HPO:0007641) Visual colour distortions(MedDRA:10047538) Dyschromatopsia(HPO:0007641) Congenital, familial and genetic disorders(MedDRA:10010331) Eye disorders congenital(MedDRA:10015920) Ocular disorders congenital NEC(MedDRA:10027673) Dyschromatopsia(HPO:0007641) |
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Database Frequency: | 19 / 7739 | |||||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
ACHROMATOPSIA 3 | (OMIM:262300) |
Autosomal dominant vitreoretinochoroidopathy | (Orphanet:3086) |
Autosomal recessive optic atrophy, OPA7 type | (Orphanet:227976) |
Autosomal recessive progressive external ophthalmoplegia | (Orphanet:254886) |
Bardet-Biedl syndrome 1 | (OMIM:209900 ) |
Bardet-Biedl syndrome 10 | (OMIM:615987) |
Bardet-Biedl syndrome 17 | (OMIM:615994) |
Benign concentric annular macular dystrophy | (Orphanet:251287) |
CONE DYSTROPHY, X-LINKED, WITH TAPETAL-LIKE SHEEN | (OMIM:304030) |
FUNDUS DYSTROPHY, PSEUDOINFLAMMATORY, RECESSIVE FORM | (OMIM:264420) |
Hereditary motor and sensory neuropathy type 6 | (Orphanet:90120) |
Leber hereditary optic neuropathy | (Orphanet:104) |
MRCS syndrome | (Orphanet:263347) |
Necrotizing encephalomyelopathy, subacute, of Leigh, adult | (OMIM:161700) |
RETINAL CONE DYSTROPHY 1 | (OMIM:180020) |
RETINAL CONE DYSTROPHY 3A | (OMIM:610024) |
Retinal macular dystrophy type 2 | (Orphanet:319640) |
Wolfram syndrome 1 | (OMIM:222300) |
Wolfram syndrome 2 | (OMIM:604928) |