Red-green dyschromatopsia
Symptom Information:
Symptom ID: | HPO:0000642 | ||||||||||||||||||||||||||||||||||||||||||||
Synonyms: |
|
||||||||||||||||||||||||||||||||||||||||||||
Quality: | |||||||||||||||||||||||||||||||||||||||||||||
Cross references: |
|
||||||||||||||||||||||||||||||||||||||||||||
Is a (Direct Parents): |
|
||||||||||||||||||||||||||||||||||||||||||||
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) |