{"context":{"query":">>hgnc>>hpo","source_dataset":"hgnc","target_dataset":"hpo"},"stats":{"queried":1,"total":100,"mapped":1},"pagination":{"has_next":true,"next_token":"-1[]HGNC:1100,10,HGNC:1100,72,2]["},"schema":"id|name|definition","mappings":[{"input":"HGNC:1100","source":"HGNC:1100|BRCA1 DNA repair associated","targets":["HP:0000006|Autosomal dominant inheritance|","HP:0000007|Autosomal recessive inheritance|","HP:0000010|Recurrent urinary tract infections|","HP:0000027|Azoospermia|","HP:0000028|Cryptorchidism|","HP:0000035|Abnormal testis morphology|","HP:0000047|Hypospadias|","HP:0000072|Hydroureter|","HP:0000079|Abnormality of the urinary system|","HP:0000083|Renal insufficiency|","HP:0000130|Abnormality of the uterus|","HP:0000135|Hypogonadism|","HP:0000175|Cleft palate|","HP:0000189|Narrow palate|","HP:0000215|Thick upper lip vermilion|","HP:0000218|High palate|","HP:0000238|Hydrocephalus|","HP:0000252|Microcephaly|","HP:0000268|Dolichocephaly|","HP:0000280|Coarse facial features|","HP:0000286|Epicanthus|","HP:0000294|Low anterior hairline|","HP:0000316|Hypertelorism|","HP:0000324|Facial asymmetry|","HP:0000340|Sloping forehead|","HP:0000347|Micrognathia|","HP:0000364|Hearing abnormality|","HP:0000365|Hearing impairment|","HP:0000377|Abnormal pinna morphology|","HP:0000426|Prominent nasal bridge|","HP:0000430|Underdeveloped nasal alae|","HP:0000453|Choanal atresia|","HP:0000463|Anteverted nares|","HP:0000478|Abnormality of the eye|","HP:0000483|Astigmatism|","HP:0000486|Strabismus|","HP:0000492|Abnormal eyelid morphology|","HP:0000504|Abnormality of vision|","HP:0000505|Visual impairment|","HP:0000508|Ptosis|","HP:0000518|Cataract|","HP:0000520|Proptosis|","HP:0000527|Long eyelashes|","HP:0000568|Microphthalmia|","HP:0000581|Blepharophimosis|","HP:0000582|Upslanted palpebral fissure|","HP:0000639|Nystagmus|","HP:0000689|Dental malocclusion|","HP:0000750|Delayed speech and language development|","HP:0000813|Bicornuate uterus|","HP:0000819|Diabetes mellitus|","HP:0000864|Abnormality of the hypothalamus-pituitary axis|","HP:0000952|Jaundice|","HP:0000989|Pruritus|","HP:0001000|Abnormality of skin pigmentation|","HP:0001053|Hypopigmented skin patches|","HP:0001172|Abnormal thumb morphology|","HP:0001199|Triphalangeal thumb|","HP:0001249|Intellectual disability|","HP:0001251|Ataxia|","HP:0001263|Global developmental delay|","HP:0001347|Hyperreflexia|","HP:0001392|Abnormality of the liver|","HP:0001426|Non-Mendelian inheritance|","HP:0001433|Hepatosplenomegaly|","HP:0001442|Typified by somatic mosaicism|","HP:0001508|Failure to thrive|","HP:0001510|Growth delay|","HP:0001511|Intrauterine growth retardation|","HP:0001537|Umbilical hernia|","HP:0001562|Oligohydramnios|","HP:0001572|Macrodontia|","HP:0001631|Atrial septal defect|","HP:0001636|Tetralogy of Fallot|","HP:0001639|Hypertrophic cardiomyopathy|","HP:0001643|Patent ductus arteriosus|","HP:0001646|Abnormal aortic valve morphology|","HP:0001671|Abnormal cardiac septum morphology|","HP:0001679|Abnormal aortic morphology|","HP:0001738|Exocrine pancreatic insufficiency|","HP:0001760|Abnormal foot morphology|","HP:0001763|Pes planus|","HP:0001770|Toe syndactyly|","HP:0001824|Weight loss|","HP:0001871|Abnormality of blood and blood-forming tissues|","HP:0001873|Thrombocytopenia|","HP:0001882|Decreased total leukocyte count|","HP:0001903|Anemia|","HP:0001945|Fever|","HP:0002007|Frontal bossing|","HP:0002017|Nausea and vomiting|","HP:0002019|Constipation|","HP:0002023|Anal atresia|","HP:0002027|Abdominal pain|","HP:0002039|Anorexia|","HP:0002119|Ventriculomegaly|","HP:0002245|Meckel diverticulum|","HP:0002251|Aganglionic megacolon|","HP:0002254|Intermittent diarrhea|","HP:0002414|Spina bifida|"]}]}