{"Name":"Cataract 35","DiseaseID__c":"GARD:0009492","id":9492,"encodedName":"cataract-35","IsDeleted":false,"Disease_Name_Full__c":"Cataract 35","Xref_IDs__c":"C1836272; C563728; DOID:0110261; MEDGEN:373050; MONDO:0012260; OMIM:609376","USA_Estimate__c":null,"No_of_Specialist_Tagsa__c":1,"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":4,"No_of_Age_at_Onset__c":0,"Description_Source__c":"MONDO:0012260","Disease_Description__c":"A cataract that has material basis in variation in the region 19q13.","GARD_Name__c":"Cataract 35","GARD_Synonym__c":"autosomal recessive congenital nuclear cataract 1; cataract 35, congenital nuclear; cataract type 35; catcn1; ctrct35","Curated_Disease_Description_Source__c":"MONDO:12260","Curated_Disease_Description__c":"Cataract 35 is cataract that has material basis in variation in the region 19q13.","Curated_USA_Estimate_Source__c":null,"Curated_USA_Estimate__c":null,"Age_at_Onset_Snippet_Text__c":null,"SourceID__c":"OMIM:609376","Deprecated__c":"No","Disease_Concept_Type__c":"Rare Disease Entity","MONDO_ID__c":"MONDO:0012260","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":"Cataract 35 is cataract that has material basis in variation in the region 19q13.","Curated_Disease_Description_Source__c":"MONDO:12260","GARD_Synonym__c":"autosomal recessive congenital nuclear cataract 1; cataract 35, congenital nuclear; cataract type 35; catcn1; ctrct35","Name":"Cataract 35","estimateUsa":""}],"GARD_Disease_Tag__c":[{"Tag_Name__c":"Anterior segment of Eye","Tag_Category__c":"Specialist","curated_tag_name":"Front part of eye disease"}],"External_Identifier_Disease__c":[{"URL__c":"https://raresource.nih.gov/diseases/filter/0009492","Source__c":"RareSource"},{"URL__c":"https://www.ncbi.nlm.nih.gov/medgen/?term=373050","Source__c":"C1836272","Xref__c":"MEDGEN:373050"},{"URL__c":"https://www.omim.org/entry/609376","Source__c":"C1836272; MONDO:0012260","Xref__c":"OMIM:609376"},{"URL__c":"https://www.ncbi.nlm.nih.gov/mesh/C563728","Source__c":"MONDO:0012260","Xref__c":"C563728"},{"URL__c":"https://uts.nlm.nih.gov/uts/umls/concept/C1836272","Source__c":"C1836272","Xref__c":"C1836272"},{"URL__c":"https://www.ebi.ac.uk/ols4/ontologies/doid/classes?obo_id=DOID%3A0110261","Source__c":"MONDO:0012260","Xref__c":"DOID:0110261"},{"URL__c":"http://purl.obolibrary.org/obo/MONDO_0012260","Source__c":"GARD:0009492","Xref__c":"MONDO:0012260"}],"Inheritance__c":["Autosomal recessive"],"GARD_Disease_Feature__c":[{"Provided_By__c":"OMIM:609376","Feature__r":{"HPO_Description__c":"A cataract is an opacity or clouding that develops in the crystalline lens of the eye or in its capsule.","HPO_Feature_URL__c":"https://hpo.jax.org/browse/term/HP:0000518","HPO_Synonym__c":"Cataracts; Clouding of the lens of the eye; Cloudy lens; Lens opacities; Lens opacity","HPO_Name__c":"Cataract","HPO_Feature_Type__c":"Symptom"}}],"tags":{"Specialist":["Anterior segment of Eye"]},"synonyms":["autosomal recessive congenital nuclear cataract 1"," cataract 35, congenital nuclear"," cataract type 35"," catcn1"," ctrct35"]}