{"context":{"query":">>hgnc>>orphanet","source_dataset":"hgnc","target_dataset":"orphanet"},"stats":{"queried":1,"total":6,"mapped":1},"pagination":{"has_next":false},"schema":"id|name|disorder_type|gene_count|phenotype_count","mappings":[{"input":"HGNC:28337","source":"HGNC:28337|C9orf72-SMCR8 complex subunit","targets":["100069|Semantic dementia|Disease|7|10","100070|Progressive non-fluent aphasia|Disease|8|32","275864|Behavioral variant of frontotemporal dementia|Disease|9|40","275872|Frontotemporal dementia with motor neuron disease|Disease|7|35","401901|Huntington disease-like syndrome due to C9ORF72 expansions|Disease|1|14","803|Amyotrophic lateral sclerosis|Disease|36|47"]}]}