{"Name":"Achromatopsia 2","DiseaseID__c":"GARD:0009649","id":9649,"encodedName":"achromatopsia-2","IsDeleted":false,"Disease_Name_Full__c":"Achromatopsia 2","Xref_IDs__c":"C168757; C1857618; C536128; DOID:0110007; MEDGEN:387867; MONDO:0009003","USA_Estimate__c":null,"No_of_Specialist_Tagsa__c":2,"No_of_ClinGen_records__c":0,"No_of_GeneReviews__c":0,"No_of_HHS_records__c":0,"World_Estimate__c":null,"No_of_HRSA_records__c":0,"Evidence_Based_Score__c":0,"No_of_Disease_Descriptions__c":2,"Disease_Characteristics_Score__c":3,"No_of_Age_at_Onset__c":0,"Description_Source__c":"MONDO:0009003","Disease_Description__c":"Achromatopsia 2 is a condition that affects the color vision. Most people have complete achromatopsia which is characterized by a total absence of color vision (only able to see black, white and shades of gray). Rarely, affected people may have incomplete achromatopsia which is associated with some color discrimination. Other common signs and symptoms include reduced visual acuity, involuntary back-and-forth eye movements, increased sensitivity to light (photophobia), and hyperopia (farsightedness). Achromatopsia 2 is caused by changes (mutations) in the CNGA3 gene and is inherited in an autosomal recessive manner. Although color discrimination cannot be improved, treatments are available to address some of the other associated symptoms.","GARD_Name__c":"Achromatopsia 2","GARD_Synonym__c":"achm2; achromatopsia caused by mutation in cnga3; achromatopsia type 2; cnga3 achromatopsia; colorblindness, total; rmch2; rod monochromacy 2; rod monochromatism 2","Curated_Disease_Description_Source__c":"GARD:0009649","Curated_Disease_Description__c":"Achromatopsia 2 is a condition that affects the color vision. Most people have complete achromatopsia which is characterized by a total absence of color vision (only able to see black, white and shades of gray). Some people may have incomplete achromatopsia which is associated with some color discrimination. Other common symptoms include reduced visual acuity, involuntary back-and-forth eye movements, increased sensitivity to light (photophobia), and hyperopia (farsightedness). Achromatopsia 2 is caused by changes in the CNGA3 gene and is inherited in an autosomal recessive manner.","Curated_USA_Estimate_Source__c":null,"Curated_USA_Estimate__c":null,"Age_at_Onset_Snippet_Text__c":null,"SourceID__c":"OMIM:216900","Deprecated__c":"No","Disease_Concept_Type__c":"Rare Disease Entity","MONDO_ID__c":"MONDO:0009003","ORPHANET_ID__c":null,"Replaced_By_ID__c":null,"Display_Spanish_Disease_Name__c":null,"Spanish_Description_Source__c":null,"Spanish_Description__c":null,"Spanish_Disease_Name__c":null,"Spanish_GARD_Synonym__c":null,"Category_Linearization__c":null,"icd10_id__c":null,"mesh_id__c":null,"omim_id__c":null,"snomed_id__c":null,"umls_id__c":null,"GARD_Disease__c":[{"Curated_Disease_Description__c":"Achromatopsia 2 is a condition that affects the color vision. Most people have complete achromatopsia which is characterized by a total absence of color vision (only able to see black, white and shades of gray). Some people may have incomplete achromatopsia which is associated with some color discrimination. Other common symptoms include reduced visual acuity, involuntary back-and-forth eye movements, increased sensitivity to light (photophobia), and hyperopia (farsightedness). Achromatopsia 2 is caused by changes in the CNGA3 gene and is inherited in an autosomal recessive manner.","Curated_Disease_Description_Source__c":"GARD:0009649","GARD_Synonym__c":"achm2; achromatopsia caused by mutation in cnga3; achromatopsia type 2; cnga3 achromatopsia; colorblindness, total; rmch2; rod monochromacy 2; rod monochromatism 2","Name":"Achromatopsia 2","estimateUsa":""}],"Organization_Supported_Diseases__c":[{"Account_Name__c":"Foundation Fighting Blindness","Website__c":"https://www.fightingblindness.org/"}],"GARD_Disease_Tag__c":[{"Tag_Name__c":"Retinal","Tag_Category__c":"Account;Specialist","curated_tag_name":"Retinal disorders"},{"Tag_Name__c":"Neuro-Ophthalmology","Tag_Category__c":"Specialist","curated_tag_name":"Neuro-ophthalmic diseases"}],"Diagnosis__c":[{"Type__c":"GTR","Curie__c":"MEDGEN:C0152200"},{"Type__c":"GTR","Curie__c":"MEDGEN:C1857618"}],"External_Identifier_Disease__c":[{"URL__c":"https://raresource.nih.gov/diseases/filter/0009649","Source__c":"RareSource"},{"URL__c":"https://www.ncbi.nlm.nih.gov/books/NBK1418","Source__c":"Gene Review","Xref__c":"NBK1418"},{"URL__c":"https://uts.nlm.nih.gov/uts/umls/concept/C1857618","Source__c":"C1857618","Xref__c":"C1857618"},{"URL__c":"https://www.ncbi.nlm.nih.gov/mesh/C536128","Source__c":"MONDO:0009003","Xref__c":"C536128"},{"URL__c":"https://evsexplore.semantics.cancer.gov/evsexplore/concept/ncit/C168757","Source__c":"C1857618; MONDO:0009003","Xref__c":"C168757"},{"URL__c":"https://www.ebi.ac.uk/ols4/ontologies/doid/classes?obo_id=DOID%3A0110007","Source__c":"MONDO:0009003","Xref__c":"DOID:0110007"},{"URL__c":"https://www.ncbi.nlm.nih.gov/medgen/?term=387867","Source__c":"C1857618","Xref__c":"MEDGEN:387867"},{"URL__c":"http://purl.obolibrary.org/obo/MONDO_0009003","Source__c":"GARD:0009649","Xref__c":"MONDO:0009003"}],"GARD_Disease_Gene__c":[{"GeneSymbol__c":"CNGA3","GHR_URL__c":"https://medlineplus.gov/genetics/gene/cnga3","Gene_Type__c":"protein-coding gene","Causal_Gene__c":true}],"tags":{"Account":["Retinal"],"Specialist":["Retinal","Neuro-Ophthalmology"]},"synonyms":["achm2"," achromatopsia caused by mutation in cnga3"," achromatopsia type 2"," cnga3 achromatopsia"," colorblindness, total"," rmch2"," rod monochromacy 2"," rod monochromatism 2"]}