{"context":{"query":">>hpo>>orphanet","source_dataset":"hpo","target_dataset":"orphanet"},"stats":{"queried":1,"total":28,"mapped":1},"pagination":{"has_next":false},"schema":"id|name|disorder_type|gene_count|phenotype_count","mappings":[{"input":"HP:0001045","source":"HP:0001045|Vitiligo","targets":["101003|Autosomal recessive spastic paraplegia type 23|Disease|2|14","140936|Lelis syndrome|Malformation syndrome|0|22","1855|Spondyloenchondrodysplasia|Malformation syndrome|1|52","199299|Late-onset isolated ACTH deficiency|Disease|0|41","2137|Autoimmune hepatitis|Disease|0|34","227982|Autoimmune polyendocrinopathy type 3|Disease|0|33","227990|Autoimmune polyendocrinopathy type 4|Disease|0|32","275|Severe combined immunodeficiency due to DCLRE1C deficiency|Disease|1|28","289390|Primary Sjögren disease|Disease|0|82","293978|Deficiency in anterior pituitary function-variable immunodeficiency syndrome|Disease|1|38","3437|Vogt-Koyanagi-Harada disease|Disease|3|37","3453|Autoimmune polyendocrinopathy type 1|Disease|1|38","468678|White-Sutton syndrome|Disease|1|72","480898|Global developmental delay-visual anomalies-progressive cerebellar atrophy-truncal hypotonia syndrome|Disease|1|31","51636|WHIM syndrome|Disease|1|34","550|MELAS|Disease|14|87","700|Alopecia totalis|Disease|0|10","701|Alopecia universalis|Disease|1|13","79098|Sympathetic ophthalmia|Disease|0|26","79153|Idiopathic trachyonychia|Disease|0|17","85138|Addison disease|Disease|0|56","881|Turner syndrome|Malformation syndrome|0|115","90289|Localized scleroderma|Disease|0|55","926|Acatalasemia|Disease|1|17","95409|Acute adrenal insufficiency|Clinical syndrome|0|44","99226|Monosomy X syndrome|Etiological subtype|0|113","99228|Mosaic monosomy X syndrome|Etiological subtype|0|113","99413|Turner syndrome due to structural X chromosome anomalies|Etiological subtype|0|113"]}]}