Red-green dyschromatopsia

Symptom Information:

Symptom ID: HPO:0000642
Synonyms:
Dyschromatopsia with red-green confusion [HPO:0000642]
RED/GREEN COLOR VISION DEFECT [HPO:0000642]
Daltonism [Orphanet:5570]
Reduced red-green discrimination (finding) [Orphanet:5570]
Daltonism (disorder) [Orphanet:5570]
Deutan defect (disorder) [Orphanet:5570]
Color Blindness, Red-Green [Orphanet:5570]
Color Blindness, Green [Orphanet:5570]
Dyschromatopsia with red-green confusion [OMIM:Dyschromatopsia with red-green confusion]
Red-green dyschromatopsia [OMIM:Red-green dyschromatopsia]
Red/green color vision defect [OMIM:Red/green color vision defect]
Achromatopsia/dyschromatopsia/daltonism/impaired colour vision [Orphanet:5570]
Red-green colour blindness [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]
Defective color vision [OMIM:Defective color vision]
Blindness colour total [MedDRA:10005175]
Achromatopsia [Orphanet:5570]
Color vision deficiency (disorder) [Orphanet:5570]
Color blindness (disorder) [Orphanet:5570]
Achromatopsia (disorder) [Orphanet:5570]
Achromatopsia 2 [Orphanet:5570]
Color blindness [Orphanet:5570]
Colour blindness (incl acquired) [MedDRA:10005174]
Red-green color defect in many patients with deletion downstream of exon 30 [OMIM,du]
Quality:
Cross references:
Orphanet:5570 "Achromatopsia/dyschromatopsia/daltonism/impaired colour vision" [Orphanet:5570]
OMIM: "Dyschromatopsia with red-green confusion" [OMIM:Dyschromatopsia with red-green confusion]
OMIM: "Red-green dyschromatopsia" [OMIM:Red-green dyschromatopsia]
OMIM: "Red/green color vision defect" [OMIM:Red/green color vision defect]
OMIM: "Defective color vision" [OMIM:Defective color vision]
UMLS:C1321726 "Daltonism (disorder)" [Orphanet:5570]
UMLS:C0155016 "Color Blindness, Red-Green" [Orphanet:5570]
UMLS:C0239777 "Color Blindness, Green" [Orphanet:5570]
UMLS:C1857618 "Achromatopsia 2" [Orphanet:5570]
UMLS:C0152200 "Achromatopsia" [Orphanet:5570]
UMLS:C0242225 "Color blindness" [Orphanet:5570]
Is a (Direct Parents):
MedDRA Vision disorders
Orphanet Abnormality of the eye
HPO         Dyschromatopsia
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)
                      Red-green dyschromatopsia(HPO:0000642)
MedDRA:
Eye disorders(MedDRA:10015919)
    Vision disorders(MedDRA:10047518)
       Red-green dyschromatopsia(HPO:0000642)
Congenital, familial and genetic disorders(MedDRA:10010331)
    Eye disorders congenital(MedDRA:10015920)
       Ocular disorders congenital NEC(MedDRA:10027673)
          Red-green dyschromatopsia(HPO:0000642)
Database Frequency: 25 / 7739
Resource:

All diseases associated with this symptom:

Adult-onset foveomacular vitelliform dystrophy (Orphanet:99000)
Autosomal dominant optic atrophy and congenital deafness (Orphanet:3212)
Autosomal dominant optic atrophy plus syndrome (Orphanet:1215)
Autosomal dominant optic atrophy, classic type (Orphanet:98673)
Autosomal recessive optic atrophy, OPA6 type (Orphanet:99012)
Bardet-Biedl syndrome 1 (OMIM:209900 )
Bardet-Biedl syndrome 10 (OMIM:615987)
Behr syndrome (Orphanet:1239)
Best vitelliform macular dystrophy (Orphanet:1243)
Beta-thalassemia major (Orphanet:231214)
Blue cone monochromatism (Orphanet:16)
CONE DYSTROPHY, X-LINKED, WITH TAPETAL-LIKE SHEEN (OMIM:304030)
Cone rod dystrophy (Orphanet:1872)
Duchenne muscular dystrophy (Orphanet:98896)
Jalili syndrome (Orphanet:1873)
Kallmann syndrome (Orphanet:478)
OPTIC ATROPHY 1 (OMIM:165500)
OPTIC ATROPHY 8 (OMIM:616289)
Progressive cone dystrophy (Orphanet:1871)
RETINAL CONE DYSTROPHY 1 (OMIM:180020)
RETINITIS PIGMENTOSA 37 (OMIM:611131)
Retinohepatoendocrinologic syndrome (Orphanet:3087)
Riboflavin transporter deficiency (Orphanet:97229)
Spondylometaphyseal dysplasia - cone-rod dystrophy (Orphanet:85167)
Wolfram-like syndrome (ORPHA:411590)