{"context":{"query":">>hgnc>>orphanet","source_dataset":"hgnc","target_dataset":"orphanet"},"stats":{"queried":1,"total":13,"mapped":1},"pagination":{"has_next":false},"schema":"id|name|disorder_type|gene_count|phenotype_count","mappings":[{"input":"HGNC:3690","source":"HGNC:3690|fibroblast growth factor receptor 3","targets":["15|Achondroplasia|Disease|1|39","1860|Thanatophoric dysplasia type 1|Clinical subtype|1|40","2363|Lacrimoauriculodentodigital syndrome|Malformation syndrome|3|63","251576|Gliosarcoma|Histopathological subtype|12|0","251579|Giant cell glioblastoma|Histopathological subtype|13|0","35099|Non-syndromic bicoronal craniosynostosis|Morphological anomaly|4|11","429|Hypochondroplasia|Disease|1|20","53271|Muenke syndrome|Malformation syndrome|1|21","794|Saethre-Chotzen syndrome|Malformation syndrome|3|61","85164|Camptodactyly-tall stature-scoliosis-hearing loss syndrome|Disease|1|4","85165|Severe achondroplasia-developmental delay-acanthosis nigricans syndrome|Disease|1|14","93262|Crouzon syndrome-acanthosis nigricans syndrome|Malformation syndrome|1|28","93274|Thanatophoric dysplasia type 2|Clinical subtype|1|35"]}]}