{"context":{"query":">>hgnc>>gencc","source_dataset":"hgnc","target_dataset":"gencc"},"stats":{"queried":1,"total":29,"mapped":1},"pagination":{"has_next":false},"schema":"id|gene_symbol|disease_title|classification_title|moi_title|submitter_title","mappings":[{"input":"HGNC:3688","source":"HGNC:3688|fibroblast growth factor receptor 1","targets":["GENCC_000101-HGNC_3688-MONDO_0014196-HP_0000006-GENCC_100002|FGFR1|Hartsfield-Bixler-Demyer syndrome|Strong|Autosomal dominant|Ambry Genetics","GENCC_000101-HGNC_3688-OMIM_147950-HP_0000006-GENCC_100001|FGFR1|hypogonadotropic hypogonadism 2 with or without anosmia|Definitive|Autosomal dominant|Ambry Genetics","GENCC_000101-HGNC_3688-OMIM_166250-HP_0000006-GENCC_100003|FGFR1|osteoglophonic dysplasia|Moderate|Autosomal dominant|Ambry Genetics","GENCC_000101-HGNC_3688-OMIM_615465-HP_0000006-GENCC_100003|FGFR1|Hartsfield-Bixler-Demyer syndrome|Moderate|Autosomal dominant|Ambry Genetics","GENCC_000104-HGNC_3688-OMIM_101600-HP_0000006-GENCC_100002|FGFR1|Pfeiffer syndrome|Strong|Autosomal dominant|Genomics England PanelApp","GENCC_000104-HGNC_3688-OMIM_123150-HP_0000006-GENCC_100002|FGFR1|Jackson-Weiss syndrome|Strong|Autosomal dominant|Genomics England PanelApp","GENCC_000104-HGNC_3688-OMIM_166250-HP_0000006-GENCC_100002|FGFR1|osteoglophonic dysplasia|Strong|Autosomal dominant|Genomics England PanelApp","GENCC_000104-HGNC_3748-OMIM_146700-HP_0000006-GENCC_100002|FLG|autosomal dominant ichthyosis vulgaris|Strong|Autosomal dominant|Genomics England PanelApp","GENCC_000106-HGNC_3688-OMIM_101600-HP_0000006-GENCC_100002|FGFR1|Pfeiffer syndrome|Strong|Autosomal dominant|Labcorp Genetics (formerly Invitae)","GENCC_000106-HGNC_3688-OMIM_147950-HP_0000006-GENCC_100002|FGFR1|hypogonadotropic hypogonadism 2 with or without anosmia|Strong|Autosomal dominant|Labcorp Genetics (formerly Invitae)","GENCC_000106-HGNC_3688-OMIM_166250-HP_0000006-GENCC_100002|FGFR1|osteoglophonic dysplasia|Strong|Autosomal dominant|Labcorp Genetics (formerly Invitae)","GENCC_000106-HGNC_3748-OMIM_146700-HP_0000006-GENCC_100002|FLG|autosomal dominant ichthyosis vulgaris|Strong|Autosomal dominant|Labcorp Genetics (formerly Invitae)","GENCC_000107-HGNC_3748-OMIM_146700-HP_0032113-GENCC_100001|FLG|autosomal dominant ichthyosis vulgaris|Definitive|Semidominant|Laboratory for Molecular Medicine","GENCC_000110-HGNC_3688-ORPHANET_2117-HP_0000006-GENCC_100009|FGFR1|Hartsfield-Bixler-Demyer syndrome|Supportive|Autosomal dominant|Orphanet","GENCC_000110-HGNC_3688-ORPHANET_2162-HP_0000007-GENCC_100009|FGFR1|holoprosencephaly|Supportive|Autosomal recessive|Orphanet","GENCC_000110-HGNC_3688-ORPHANET_2645-HP_0000006-GENCC_100009|FGFR1|osteoglophonic dysplasia|Supportive|Autosomal dominant|Orphanet","GENCC_000110-HGNC_3688-ORPHANET_3157-HP_0000006-GENCC_100009|FGFR1|septooptic dysplasia|Supportive|Autosomal dominant|Orphanet","GENCC_000110-HGNC_3688-ORPHANET_3366-HP_0000006-GENCC_100009|FGFR1|isolated trigonocephaly|Supportive|Autosomal dominant|Orphanet","GENCC_000110-HGNC_3688-ORPHANET_432-HP_0000006-GENCC_100009|FGFR1|hypogonadotropic hypogonadism|Supportive|Autosomal dominant|Orphanet","GENCC_000110-HGNC_3688-ORPHANET_478-HP_0000006-GENCC_100009|FGFR1|Kallmann syndrome|Supportive|Autosomal dominant|Orphanet","GENCC_000110-HGNC_3688-ORPHANET_93258-HP_0000006-GENCC_100009|FGFR1|Pfeiffer syndrome type 1|Supportive|Autosomal dominant|Orphanet","GENCC_000110-HGNC_3688-ORPHANET_99798-HP_0000006-GENCC_100009|FGFR1|tooth agenesis|Supportive|Autosomal dominant|Orphanet","GENCC_000110-HGNC_3748-ORPHANET_461-HP_0001417-GENCC_100009|FLG|recessive X-linked ichthyosis|Supportive|X-linked|Orphanet","GENCC_000112-HGNC_3688-OMIM_101600-HP_0000006-GENCC_100001|FGFR1|Pfeiffer syndrome|Definitive|Autosomal dominant|G2P","GENCC_000112-HGNC_3688-OMIM_147950-HP_0000006-GENCC_100001|FGFR1|hypogonadotropic hypogonadism 2 with or without anosmia|Definitive|Autosomal dominant|G2P","GENCC_000112-HGNC_3688-OMIM_166250-HP_0000006-GENCC_100001|FGFR1|osteoglophonic dysplasia|Definitive|Autosomal dominant|G2P","GENCC_000112-HGNC_3688-OMIM_613001-HP_0000006-GENCC_100001|FGFR1|encephalocraniocutaneous lipomatosis|Definitive|Autosomal dominant|G2P","GENCC_000112-HGNC_3688-OMIM_615465-HP_0000006-GENCC_100001|FGFR1|Hartsfield-Bixler-Demyer syndrome|Definitive|Autosomal dominant|G2P","GENCC_000112-HGNC_3748-OMIM_146700-HP_0000007-GENCC_100004|FLG|autosomal dominant ichthyosis vulgaris|Limited|Autosomal recessive|G2P"]}]}