Abnormality of color vision
Symptom Information:
Symptom ID: | HPO:0000551 | |||||
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) MedDRA: |
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Database Frequency: | 20 / 7739 | |||||
Resource: |
All diseases associated with this symptom:
CONE-ROD DYSTROPHY 13 | (OMIM:608194) |
CONE-ROD DYSTROPHY 15 | (OMIM:613660) |
CONE-ROD DYSTROPHY 20 | (OMIM:615973) |
CONE-ROD DYSTROPHY 3 | (OMIM:604116) |
CONE-ROD DYSTROPHY 5 | (OMIM:600977) |
CONE-ROD DYSTROPHY 7 | (OMIM:603649) |
CONE-ROD DYSTROPHY, X-LINKED, 3 | (OMIM:300476) |
Cone rod dystrophy | (Orphanet:1872) |
Hereditary motor and sensory neuropathy type 6 | (Orphanet:90120) |
Leber congenital amaurosis 15 | (OMIM:613843) |
Leber plus disease | (Orphanet:99718) |
MRCS syndrome | (Orphanet:263347) |
NEWFOUNDLAND ROD-CONE DYSTROPHY | (OMIM:607476) |
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B | (OMIM:610427) |
Neurodegeneration with brain iron accumulation due to C19orf12 mutation | (Orphanet:289560) |
Progressive cone dystrophy | (Orphanet:1871) |
RETINITIS PIGMENTOSA 23 | (OMIM:300424) |
Retinitis pigmentosa 10 | (OMIM:180105) |
Wolfram syndrome 1 | (OMIM:222300) |
Wolfram-like syndrome | (ORPHA:411590) |