{"context":{"query":">>ensembl>>hpo","source_dataset":"ensembl","target_dataset":"hpo"},"stats":{"queried":1,"total":93,"mapped":1},"pagination":{"has_next":false},"schema":"id|name|definition","mappings":[{"input":"ENSG00000169083","source":"ENSG00000169083|AR","targets":["HP:0000008|Abnormal morphology of female internal genitalia|","HP:0000023|Inguinal hernia|","HP:0000027|Azoospermia|","HP:0000028|Cryptorchidism|","HP:0000029|Testicular atrophy|","HP:0000037|Male pseudohermaphroditism|","HP:0000047|Hypospadias|","HP:0000048|Bifid scrotum|","HP:0000051|Perineal hypospadias|","HP:0000054|Micropenis|","HP:0000062|Ambiguous genitalia|","HP:0000066|Labial hypoplasia|","HP:0000098|Tall stature|","HP:0000135|Hypogonadism|","HP:0000144|Decreased fertility|","HP:0000151|Aplasia of the uterus|","HP:0000153|Abnormality of the mouth|","HP:0000175|Cleft palate|","HP:0000716|Depression|","HP:0000739|Anxiety|","HP:0000763|Sensory neuropathy|","HP:0000771|Gynecomastia|","HP:0000776|Congenital diaphragmatic hernia|","HP:0000786|Primary amenorrhea|","HP:0000789|Infertility|","HP:0000818|Abnormality of the endocrine system|","HP:0000823|Delayed puberty|","HP:0001061|Acne|","HP:0001252|Hypotonia|","HP:0001260|Dysarthria|","HP:0001265|Hyporeflexia|","HP:0001283|Bulbar palsy|","HP:0001288|Gait disturbance|","HP:0001337|Tremor|","HP:0001417|X-linked inheritance|","HP:0001419|X-linked recessive inheritance|","HP:0001507|Growth abnormality|","HP:0001518|Small for gestational age|","HP:0001539|Omphalocele|","HP:0001547|Abnormal rib cage morphology|","HP:0001618|Dysphonia|","HP:0001620|Abnormally high-pitched voice|","HP:0002015|Dysphagia|","HP:0002023|Anal atresia|","HP:0002032|Esophageal atresia|","HP:0002215|Sparse axillary hair|","HP:0002221|Absent axillary hair|","HP:0002225|Sparse pubic hair|","HP:0002380|Fasciculations|","HP:0002550|Absent facial hair|","HP:0002555|Absent pubic hair|","HP:0002664|Neoplasm|","HP:0003119|Abnormal circulating lipid concentration|","HP:0003202|Skeletal muscle atrophy|","HP:0003236|Elevated circulating creatine kinase concentration|","HP:0003251|Male infertility|","HP:0003394|Muscle spasm|","HP:0003577|Congenital onset|","HP:0003581|Adult onset|","HP:0003677|Slowly progressive|","HP:0003690|Limb muscle weakness|","HP:0005978|Type II diabetes mellitus|","HP:0008189|Insulin insensitivity|","HP:0008226|Androgen insufficiency|","HP:0008232|Elevated circulating follicle stimulating hormone level|","HP:0008655|Aplasia/Hypoplasia of the fallopian tube|","HP:0008665|Clitoral hypertrophy|","HP:0008689|Bilateral cryptorchidism|","HP:0008722|Urethral diverticulum|","HP:0008730|Female external genitalia in individual with 46,XY karyotype|","HP:0008981|Calf muscle hypertrophy|","HP:0009830|Peripheral neuropathy|","HP:0009888|Abnormality of secondary sexual hair|","HP:0010463|Aplasia of the ovary|","HP:0010788|Testicular neoplasm|","HP:0011969|Elevated circulating luteinizing hormone level|","HP:0012125|Prostate cancer|","HP:0012435|Ventral shortening of foreskin|","HP:0012873|Absent vas deferens|","HP:0012888|Abnormal uterine cervix morphology|","HP:0025132|Abnormal circulating estrogen level|","HP:0025134|Increased serum estradiol|","HP:0025486|Fused labia majora|","HP:0030088|Increased serum testosterone level|","HP:0030346|Abnormal circulating follicle-stimulating hormone concentration|","HP:0031102|Increased circulating antimullerian hormone concentration|","HP:0040307|Male sexual dysfunction|","HP:0040314|Blind vagina|","HP:0100022|Abnormality of movement|","HP:0100627|Displacement of the urethral meatus|","HP:0100639|Erectile dysfunction|","HP:0100728|Germ cell neoplasia|","HP:0100779|Urogenital sinus anomaly|"]}]}