Dyschromatopsia

Symptom Information:

Symptom ID: HPO:0007641
Synonyms:
Color vision deficiency (disorder) [Orphanet:5570]
Color vision defect [Orphanet:5570]
Dyschromatopsia [Orphanet:5570]
Color blindness [Orphanet:5570]
Dyschromatopsia [OMIM:Dyschromatopsia]
Achromatopsia/dyschromatopsia/daltonism/impaired colour vision [Orphanet:5570]
Defective color vision [Orphanet:5570]
Colour blindness [MedDRA:10010050]
Achromatopsia [MedDRA:10010050]
Blindness color [MedDRA:10010050]
Blindness colour [MedDRA:10010050]
Blindness colour total [MedDRA:10010050]
Color blindness [MedDRA:10010050]
Color blindness NOS [MedDRA:10010050]
Color vision deficiencies [MedDRA:10010050]
Colour blindness NOS [MedDRA:10010050]
Colour vision deficiencies [MedDRA:10010050]
Defective colour vision [MedDRA:10010050]
Defective coulour vision [MedDRA:10010050]
Deutan defect [MedDRA:10010050]
Other color vision deficiencies [MedDRA:10010050]
Protan defect [MedDRA:10010050]
Tritan defect [MedDRA:10010050]
Blindness color total [MedDRA:10010050]
Defective color vision [MedDRA:10010050]
Daltonism [MedDRA:10010050]
Red-green colour blindness [MedDRA:10010050]
Deuteranopia [MedDRA:10010050]
Chromatopsia [MedDRA:10008795]
Dyschromatopsia [MedDRA:10008795]
Vision color tinged [MedDRA:10008795]
Color vision defects [OMIM:Color vision defects]
Defective color vision [OMIM:Defective color vision]
Dyschromatopsia (1 patient) [OMIM:Dyschromatopsia (1 patient)]
Dyschromatopsia (some) [OMIM:Dyschromatopsia (some)]
Blindness colour total [MedDRA:10005175]
Achromatopsia [Orphanet:5570]
Color blindness (disorder) [Orphanet:5570]
Achromatopsia (disorder) [Orphanet:5570]
Achromatopsia 2 [Orphanet:5570]
Colour blindness (incl acquired) [MedDRA:10005174]
Quality:
Cross references:
Orphanet:5570 "Achromatopsia/dyschromatopsia/daltonism/impaired colour vision" [Orphanet:5570]
OMIM: "Dyschromatopsia" [OMIM:Dyschromatopsia]
OMIM: "Color vision defects" [OMIM:Color vision defects]
OMIM: "Defective color vision" [OMIM:Defective color vision]
OMIM: "Dyschromatopsia (1 patient)" [OMIM:Dyschromatopsia (1 patient)]
OMIM: "Dyschromatopsia (some)" [OMIM:Dyschromatopsia (some)]
UMLS:C0009398 "Color vision defect" [Orphanet:5570]
UMLS:C0858618 "Dyschromatopsia" [Orphanet:5570]
UMLS:C0242225 "Color blindness" [Orphanet:5570]
UMLS:C1857618 "Achromatopsia 2" [Orphanet:5570]
UMLS:C0152200 "Achromatopsia" [Orphanet:5570]
Is a (Direct Parents):
Orphanet Red-green dyschromatopsia
MedDRA Visual colour distortions
Orphanet Abnormality of the eye
HPO         Abnormality of color vision
MedDRA Vision disorders
MedDRA Ocular disorders congenital NEC
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)
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)