{"Name":"Familial chronic myelocytic leukemia-like syndrome","DiseaseID__c":"GARD:0010141","id":10141,"encodedName":"familial-chronic-myelocytic-leukemia-like-syndrome","IsDeleted":false,"Disease_Name_Full__c":"Familial chronic myelocytic leukemia-like syndrome","Xref_IDs__c":"C1838670; C536093; DOID:0060761; MEDGEN:325075; MONDO:0010809; OMIM:600080","USA_Estimate__c":null,"No_of_Specialist_Tagsa__c":0,"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":1,"Disease_Characteristics_Score__c":3,"No_of_Age_at_Onset__c":0,"Description_Source__c":"MONDO:0010809","Disease_Description__c":"A chronic myeloid leukemia characterized by chronic myelocytic leukemia in early infancy and absence of the BCR/ABL fusion gene (Philadelphia chromosome).","GARD_Name__c":"Familial chronic myelocytic leukemia-like syndrome","GARD_Synonym__c":"cml-like syndrome, familial; familial cml-like syndrome","Curated_Disease_Description_Source__c":"MONDO:0010809","Curated_Disease_Description__c":"A chronic myeloid leukemia characterized by chronic myelocytic leukemia in early infancy and absence of the BCR/ABL fusion gene (Philadelphia chromosome).","Curated_USA_Estimate_Source__c":null,"Curated_USA_Estimate__c":null,"Age_at_Onset_Snippet_Text__c":null,"SourceID__c":null,"Deprecated__c":"No","Disease_Concept_Type__c":"Rare Disease Entity","MONDO_ID__c":"MONDO:0010809","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":"A chronic myeloid leukemia characterized by chronic myelocytic leukemia in early infancy and absence of the BCR/ABL fusion gene (Philadelphia chromosome).","Curated_Disease_Description_Source__c":"MONDO:0010809","GARD_Synonym__c":"cml-like syndrome, familial; familial cml-like syndrome","Name":"Familial chronic myelocytic leukemia-like syndrome","estimateUsa":""}],"Organization_Supported_Diseases__c":[{"Account_Name__c":"The Leukemia & Lymphoma Society","Website__c":"www.lls.org"}],"GARD_Disease_Tag__c":[{"Tag_Name__c":"Cancer","Tag_Category__c":"Disease Category","category_description":"Cancer is a disease in which some of the body's cells grow uncontrollably and can spread to other parts of the body.","curated_tag_name":"Cancer"}],"External_Identifier_Disease__c":[{"URL__c":"https://www.ncbi.nlm.nih.gov/medgen/?term=325075","Source__c":"C1838670","Xref__c":"MEDGEN:325075"},{"URL__c":"https://www.ebi.ac.uk/ols4/ontologies/doid/classes?obo_id=DOID%3A0060761","Source__c":"MONDO:0010809","Xref__c":"DOID:0060761"},{"URL__c":"https://www.ncbi.nlm.nih.gov/mesh/C536093","Source__c":"MONDO:0010809","Xref__c":"C536093"},{"URL__c":"https://uts.nlm.nih.gov/uts/umls/concept/C1838670","Source__c":"C1838670","Xref__c":"C1838670"},{"URL__c":"https://www.omim.org/entry/600080","Source__c":"C1838670; MONDO:0010809","Xref__c":"OMIM:600080"},{"URL__c":"http://purl.obolibrary.org/obo/MONDO_0010809","Source__c":"GARD:0010141","Xref__c":"MONDO:0010809"}],"Inheritance__c":["Autosomal dominant"],"GARD_Disease_Feature__c":[{"Provided_By__c":"OMIM:600080","Feature__r":{"HPO_Description__c":"A myeloproliferative disorder characterized by increased proliferation of the granulocytic cell line without the loss of their capacity to differentiate.","HPO_Feature_URL__c":"https://hpo.jax.org/browse/term/HP:0005506","HPO_Synonym__c":"Chronic myelocytic leukemia; Chronic myeloid leukemia","HPO_Name__c":"Chronic myelogenous leukemia","Feature_System__c":"Immune System; Blood and Blood-Forming Tissue","HPO_Feature_Type__c":"Symptom"}}],"tags":{"Disease Category":["Cancer"]},"synonyms":["cml-like syndrome, familial"," familial cml-like syndrome"]}