{"context":{"query":">>mondo>>hpo>>orphanet","source_dataset":"mondo","target_dataset":"orphanet"},"stats":{"queried":1,"total":57,"mapped":1},"pagination":{"has_next":false},"schema":"id|name|disorder_type|gene_count|phenotype_count","mappings":[{"input":"MONDO:0004979","source":"MONDO:0004979|asthma","targets":["10|48,XXYY syndrome|Malformation syndrome|0|61","100079|Neuroendocrine neoplasm of appendix|Disease|0|30","100093|Carcinoid syndrome|Clinical syndrome|1|27","110|Bardet-Biedl syndrome|Disease|26|95","1163|Aspergillosis|Disease|0|56","1164|Allergic bronchopulmonary aspergillosis|Disease|0|14","183|Eosinophilic granulomatosis with polyangiitis|Disease|0|66","183675|Recurrent infections associated with rare immunoglobulin isotypes deficiency|Disease|2|47","2070|Eosinophilic gastroenteritis|Disease|0|21","209905|Brain-lung-thyroid syndrome|Disease|1|60","217390|Combined immunodeficiency due to DOCK8 deficiency|Disease|1|18","2257|Primary pulmonary hypoplasia|Morphological anomaly|0|26","235|Dubowitz syndrome|Malformation syndrome|2|102","251061|7q31 microdeletion syndrome|Malformation syndrome|1|50","2623|Geleophysic dysplasia|Malformation syndrome|3|47","2714|Oculo-palato-cerebral syndrome|Malformation syndrome|0|24","274|Bernard-Soulier syndrome|Disease|3|21","280200|Microform holoprosencephaly|Malformation syndrome|16|35","2902|Idiopathic chronic eosinophilic pneumonia|Disease|0|27","293939|Distal Xq28 microduplication syndrome|Malformation syndrome|0|43","293987|Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome|Disease|0|67","3206|Stüve-Wiedemann syndrome|Malformation syndrome|1|44","3260|Idiopathic hypereosinophilic syndrome|Disease|0|78","330015|Lead poisoning|Disease|0|62","331235|Selective IgM deficiency|Disease|0|64","353277|Rubinstein-Taybi syndrome due to CREBBP mutations|Etiological subtype|1|122","353281|Rubinstein-Taybi syndrome due to 16p13.3 microdeletion|Etiological subtype|1|88","353284|Rubinstein-Taybi syndrome due to EP300 haploinsufficiency|Etiological subtype|1|123","397590|Silver-Russell syndrome due to a point mutation|Etiological subtype|4|36","400|Cystic echinococcosis|Disease|0|41","443811|PGM3-CDG|Disease|1|63","444077|Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome|Malformation syndrome|1|79","449400|IgG4-related aortitis|Clinical subtype|0|25","457485|Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome|Malformation syndrome|1|45","466943|WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome|Malformation syndrome|0|70","466950|Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation|Clinical subtype|1|68","488632|TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome|Malformation syndrome|1|73","495818|9q33.3q34.11 microdeletion syndrome|Malformation syndrome|2|53","500055|Hao-Fountain syndrome due to 16p13.2 microdeletion|Etiological subtype|1|53","528647|Hereditary angioedema with normal C1Inh|Disease|0|13","544488|Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome|Disease|1|56","563|Peripartum cardiomyopathy|Disease|0|45","567|22q11.2 deletion syndrome|Malformation syndrome|10|131","586|Cystic fibrosis|Disease|19|35","60|Alpha-1-antitrypsin deficiency|Disease|1|21","60030|Loeys-Dietz syndrome|Malformation syndrome|7|38","634|Netherton syndrome|Disease|1|31","70593|Immunodeficiency due to selective anti-polysaccharide antibody deficiency|Disease|0|19","79328|ALG9-CDG|Disease|1|86","79345|Brachytelephalangic chondrodysplasia punctata|Malformation syndrome|1|56","8|47,XYY syndrome|Malformation syndrome|0|45","90280|Chilblain lupus|Disease|0|18","96263|48,XXXY syndrome|Malformation syndrome|0|62","96264|49,XXXXY syndrome|Malformation syndrome|0|64","97287|Bronchial neuroendocrine tumor|Disease|0|31","99329|48,XYYY syndrome|Malformation syndrome|0|31","99735|Myotonia permanens|Disease|1|21"]}]}