{"context":{"query":">>hpo>>orphanet","source_dataset":"hpo","target_dataset":"orphanet"},"stats":{"queried":1,"total":100,"mapped":1},"pagination":{"has_next":true,"next_token":"-1[]HP:0007018,74,HP:0007018,0,1]["},"schema":"id|name|disorder_type|gene_count|phenotype_count","mappings":[{"input":"HP:0007018","source":"HP:0007018|Attention deficit hyperactivity disorder","targets":["10|48,XXYY syndrome|Malformation syndrome|0|61","1001|2q37 microdeletion syndrome|Malformation syndrome|1|52","137605|Legius syndrome|Malformation syndrome|1|42","137831|X-linked intellectual disability-cerebellar hypoplasia syndrome|Disease|1|33","138|CHARGE syndrome|Malformation syndrome|2|94","144|Lynch syndrome|Disease|9|62","157850|Pantothenate kinase-associated neurodegeneration|Disease|0|60","1596|Distal deletion 15q syndrome|Malformation syndrome|1|59","163976|X-linked intellectual disability, Van Esch type|Malformation syndrome|1|21","1711|Mosaic trisomy 17 syndrome|Malformation syndrome|0|20","1713|17p11.2 microduplication syndrome|Malformation syndrome|1|35","1715|Trisomy 18p syndrome|Malformation syndrome|0|28","1727|22q11.2 duplication syndrome|Malformation syndrome|1|40","177907|Prader-Willi syndrome due to translocation|Etiological subtype|1|93","1929|Rasmussen subacute encephalitis|Disease|0|48","1942|Epilepsy with myoclonic-atonic seizures|Disease|7|44","1945|Self-limited epilepsy with centrotemporal spikes|Disease|3|21","199|Cornelia de Lange syndrome|Malformation syndrome|6|100","199318|15q13.3 microdeletion syndrome|Malformation syndrome|1|21","2044|Floating-Harbor syndrome|Malformation syndrome|1|79","206443|Late-infantile/juvenile Krabbe disease|Clinical subtype|1|46","2072|Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome|Clinical subtype|1|57","2073|Narcolepsy type 1|Disease|8|30","210548|Macrocephaly-intellectual disability-autism syndrome|Disease|2|24","216866|Classic pantothenate kinase-associated neurodegeneration|Clinical subtype|1|28","217340|17q21.31 microduplication syndrome|Malformation syndrome|0|25","220386|Semilobar holoprosencephaly|Clinical subtype|18|72","221008|Rothmund-Thomson syndrome type 1|Clinical subtype|1|64","228399|8q12 microduplication syndrome|Malformation syndrome|0|20","23|Argininosuccinic aciduria|Disease|1|51","2308|Jacobsen syndrome|Malformation syndrome|1|76","235|Dubowitz syndrome|Malformation syndrome|2|102","238446|15q11q13 microduplication syndrome|Malformation syndrome|1|19","2461|Marden-Walker syndrome|Malformation syndrome|1|61","250989|1q21.1 microdeletion syndrome|Malformation syndrome|0|47","250994|1q21.1 microduplication syndrome|Malformation syndrome|0|25","251019|2q32q33 deletion syndrome|Malformation syndrome|1|43","251071|8p23.1 microdeletion syndrome|Malformation syndrome|1|49","254351|Distal 7q11.23 microdeletion syndrome|Malformation syndrome|0|12","261102|Distal 7q11.23 microduplication syndrome|Malformation syndrome|0|14","261183|15q11.2 microdeletion syndrome|Malformation syndrome|3|31","261197|Proximal 16p11.2 microdeletion syndrome|Malformation syndrome|1|52","261204|16p11.2p12.2 microduplication syndrome|Malformation syndrome|0|14","261222|Distal 16p11.2 microdeletion syndrome|Malformation syndrome|1|26","261229|14q11.2 microduplication syndrome|Malformation syndrome|2|24","261243|16p13.11 microduplication syndrome|Malformation syndrome|0|19","261330|Distal 22q11.2 microdeletion syndrome|Malformation syndrome|3|60","261337|Distal 22q11.2 microduplication syndrome|Malformation syndrome|0|57","261349|2p15p16.1 microdeletion syndrome|Malformation syndrome|0|77","2637|Microcephalic osteodysplastic primordial dwarfism type II|Malformation syndrome|1|52","268947|Unilateral focal polymicrogyria|Clinical subtype|0|29","276198|Spinocerebellar ataxia type 36|Disease|1|27","276413|10q22.3q23.3 microdeletion syndrome|Malformation syndrome|0|30","280397|Familial Alzheimer-like prion disease|Disease|1|12","281090|Syndromic recessive X-linked ichthyosis|Disease|1|21","284169|Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion|Clinical subtype|1|46","284180|Xp22.13p22.2 duplication syndrome|Malformation syndrome|0|34","293939|Distal Xq28 microduplication syndrome|Malformation syndrome|0|43","3000|Familial peripheral male-limited precocious puberty|Disease|1|11","300573|Polymicrogyria due to TUBB2B mutation|Malformation syndrome|1|30","313892|Developmental and speech delay due to SOX5 deficiency|Clinical subtype|1|31","3166|Sialuria|Disease|1|36","3205|Sturge-Weber syndrome|Malformation syndrome|1|51","324313|9p13 microdeletion syndrome|Malformation syndrome|0|32","33|Isovaleric acidemia|Disease|1|29","330015|Lead poisoning|Disease|0|62","3375|Trisomy X syndrome|Malformation syndrome|0|31","3465|Worster-Drought syndrome|Disease|0|18","352490|Autism spectrum disorder due to AUTS2 deficiency|Disease|1|55","357001|19p13.13 microdeletion syndrome|Malformation syndrome|0|47","35878|Hyperinsulinism-hyperammonemia syndrome|Disease|1|12","363700|Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion|Etiological subtype|1|71","369873|Obesity due to SIM1 deficiency|Etiological subtype|1|17","370079|Proximal 16p11.2 microduplication syndrome|Malformation syndrome|0|38","38874|Dihydropyrimidinuria|Disease|1|20","391372|FOXP1 Syndrome|Malformation syndrome|1|60","397590|Silver-Russell syndrome due to a point mutation|Etiological subtype|4|36","401777|Optic atrophy-intellectual disability syndrome|Disease|1|39","401986|1p31p32 microdeletion syndrome|Malformation syndrome|1|18","404448|Helsmoortel-Van der Aa syndrome|Malformation syndrome|1|80","43|X-linked adrenoleukodystrophy|Disease|0|36","435638|3p25.3 microdeletion syndrome|Malformation syndrome|2|51","440437|Familial colorectal cancer Type X|Disease|10|53","442835|Non-specific early-onset epileptic encephalopathy|Disease|54|48","444002|11q22.2q22.3 microdeletion syndrome|Malformation syndrome|0|44","447788|Cerebral visual impairment|Clinical syndrome|0|41","459061|Craniofacial dysplasia-short stature-ectodermal anomalies-intellectual disability syndrome|Malformation syndrome|2|40","461|Recessive X-linked ichthyosis|Disease|2|12","464|Incontinentia pigmenti|Malformation syndrome|1|67","464311|Intellectual disability syndrome due to a DYRK1A point mutation|Etiological subtype|1|68","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","467166|Tubulinopathy-associated dysgyria|Disease|3|24","476126|Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome|Malformation syndrome|1|55","485405|16p12.1p12.3 triplication syndrome|Malformation syndrome|0|44","488618|Transketolase deficiency|Malformation syndrome|1|27","494344|RERE-related neurodevelopmental syndrome|Malformation syndrome|1|52","495875|Congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome|Malformation syndrome|1|52","500055|Hao-Fountain syndrome due to 16p13.2 microdeletion|Etiological subtype|1|53","506358|Gabriele-de Vries syndrome|Malformation syndrome|1|73"]}]}