Abnormality of color vision

Symptom Information:

Symptom ID: HPO:0000551
Synonyms:
Abnormal color vision [HPO:0000551]
Color vision defect [HPO:0000551]
COLOR VISION DEFECT, SEVERE [HPO:0000551]
Color vision defect, severe [OMIM:Color vision defect, severe]
Color vision defects [OMIM:Color vision defects]
Quality:
Cross references:
OMIM: "Color vision defect, severe" [OMIM:Color vision defect, severe]
OMIM: "Color vision defects" [OMIM:Color vision defects]
Is a (Direct Parents):
HPO         Color vision test abnormality
HPO         Abnormality of 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)
MedDRA:
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)