{"context":{"query":">>hgnc>>orphanet","source_dataset":"hgnc","target_dataset":"orphanet"},"stats":{"queried":1,"total":17,"mapped":1},"pagination":{"has_next":false},"schema":"id|name|disorder_type|gene_count|phenotype_count","mappings":[{"input":"HGNC:3688","source":"HGNC:3688|fibroblast growth factor receptor 1","targets":["168953|Myeloid/lymphoid neoplasm associated with FGFR1 rearrangement|Disease|1|0","2117|Hartsfield syndrome|Malformation syndrome|1|17","220386|Semilobar holoprosencephaly|Clinical subtype|18|72","2396|Encephalocraniocutaneous lipomatosis|Disease|2|55","251576|Gliosarcoma|Histopathological subtype|12|0","251579|Giant cell glioblastoma|Histopathological subtype|13|0","251615|Pilomyxoid astrocytoma|Histopathological subtype|8|0","2645|Osteoglosphonic dysplasia|Malformation syndrome|1|20","280200|Microform holoprosencephaly|Malformation syndrome|16|35","314950|Primary hypereosinophilic syndrome|Disease|5|0","3157|Septo-optic dysplasia spectrum|Malformation syndrome|7|33","3366|Non-syndromic metopic craniosynostosis|Morphological anomaly|2|12","432|Normosmic congenital hypogonadotropic hypogonadism|Clinical subtype|18|38","478|Kallmann syndrome|Clinical subtype|22|44","93258|Pfeiffer syndrome type 1|Clinical subtype|2|21","93924|Lobar holoprosencephaly|Clinical subtype|16|72","99798|Oligodontia|Morphological anomaly|12|23"]}]}