Patent ductus arteriosus
Symptom Information:
Symptom ID: | HPO:0001643 | ||||||||||||||||||||
Synonyms: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the cardiovascular system(HPO:0001626) Abnormal heart morphology(HPO:0001627) obsolete Malformation of the heart and great vessels(HPO:0002564) Congenital malformation of the great arteries(HPO:0011603) Patent ductus arteriosus(HPO:0001643) MedDRA: Vascular disorders(MedDRA:10047065) Vascular disorders NEC(MedDRA:10047066) Vascular malformations and acquired anomalies(MedDRA:10047091) Patent ductus arteriosus(HPO:0001643) |
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Database Frequency: | 228 / 7739 | ||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
10q22.3q23.3 microdeletion syndrome | (Orphanet:276413) |
14q11.2 microdeletion syndrome | (Orphanet:261120) |
17q23.1q23.2 microdeletion syndrome | (Orphanet:261279) |
1p36 deletion syndrome | (Orphanet:1606) |
1q21.1 microdeletion syndrome | (Orphanet:250989) |
22q11.2 deletion syndrome | (Orphanet:567) |
3q29 microdeletion syndrome | (Orphanet:65286) |
6p22 microdeletion syndrome | (Orphanet:251046) |
8p11.2 deletion syndrome | (Orphanet:251066) |
8p23.1 microdeletion syndrome | (Orphanet:251071) |
ADAMS-OLIVER SYNDROME 4 | (OMIM:615297) |
AGENESIS OF THE CORPUS CALLOSUM AND CONGENITAL LYMPHEDEMA | (OMIM:613623) |
AMASTIA, BILATERAL, WITH URETERAL TRIPLICATION AND DYSMORPHISM | (OMIM:104350) |
AORTIC ANEURYSM, FAMILIAL THORACIC 4 | (OMIM:132900) |
AXENFELD-RIEGER SYNDROME, TYPE 3 | (OMIM:602482) |
Acro-cardio-facial syndrome | (Orphanet:2008) |
Acroosteolysis, dominant type | (Orphanet:955) |
Agenesis of the corpus callosum - intellectual deficit - coloboma - micrognathia | (Orphanet:52055) |
Alpha-thalassemia - intellectual deficit syndrome linked to chromosome 16 | (Orphanet:98791) |
Alport syndrome - intellectual deficit - midface hypoplasia - elliptocytosis | (Orphanet:86818) |
Alström syndrome | (Orphanet:64) |
Aneurysm - osteoarthritis syndrome | (Orphanet:284984) |
Ankyloblepharon - ectodermal defects - cleft lip/palate | (Orphanet:1071) |
Anophthalmia/microphthalmia - esophageal atresia | (Orphanet:77298) |
Aphalangy - hemivertebrae - urogenital-intestinal dysgenesis | (Orphanet:1112) |
Autosomal dominant Opitz G/BBB syndrome | (Orphanet:306588) |
Autosomal dominant coarctation of aorta | (Orphanet:1455) |
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency | (Orphanet:331176) |
BARAITSER-WINTER SYNDROME 1 | (OMIM:243310) |
Baraitser-Winter syndrome | (Orphanet:2995) |
Beckwith-Wiedemann syndrome due to 11p15 microdeletion | (Orphanet:231127) |
Beckwith-Wiedemann syndrome due to 11p15 microduplication | (Orphanet:96076) |
Beckwith-Wiedemann syndrome due to CDKN1C mutation | (Orphanet:231120) |
Blepharophimosis-intellectual deficit syndrome, SBBYS type | (Orphanet:3047) |
Bone dysplasia, lethal Holmgren type | (Orphanet:1842) |
Braddock syndrome | (Orphanet:52047) |
C syndrome | (Orphanet:1308) |
CAMPTODACTYLY WITH FIBROUS TISSUE HYPERPLASIA AND SKELETAL DYSPLASIA | (OMIM:211930) |
CARPENTER SYNDROME 1 | (OMIM:201000) |
CARPENTER SYNDROME 2 | (OMIM:614976) |
CHARGE syndrome | (Orphanet:138) |
COENZYME Q10 DEFICIENCY, PRIMARY, 7 | (OMIM:616276) |
COFFIN-SIRIS SYNDROME | (OMIM:135900) |
Camptodactyly - fibrous tissue hyperplasia - skeletal dysplasia | (Orphanet:1321) |
Cantrell pentalogy | (Orphanet:1335) |
Carpenter syndrome | (Orphanet:65759) |
Cerebro-facio-thoracic dysplasia | (Orphanet:1394) |
Char syndrome | (Orphanet:46627) |
Cholestasis - pigmentary retinopathy - cleft palate | (Orphanet:1415) |
Chronic intestinal pseudo-obstruction | (Orphanet:2978) |
Cleft lip/palate - intestinal malrotation - cardiopathy | (Orphanet:2001) |
Coffin-Siris syndrome | (Orphanet:1465) |
Combined oxidative phosphorylation defect type 2 | (Orphanet:254920) |
Congenital alveolar capillary dysplasia | (Orphanet:210122) |
Congenital contractural arachnodactyly | (Orphanet:115) |
Congenital heart block | (Orphanet:60041) |
Congenital pericardium anomaly | (Orphanet:2846) |
Congenital rubella syndrome | (Orphanet:290) |
Congenital short bowel syndrome | (Orphanet:2301) |
Congenital unilateral hypoplasia of depressor anguli oris | (Orphanet:1166) |
Conotruncal heart malformations | (Orphanet:2445) |
Corneal anesthesia - deafness - intellectual deficit | (Orphanet:1051) |
Cranio-osteoarthropathy | (Orphanet:1525) |
Craniofacial dyssynostosis | (Orphanet:1516) |
Craniosynostosis - hydrocephalus - Chiari I malformation - radioulnar synostosis | (Orphanet:171839) |
Cutis laxa | (Orphanet:209) |
Cutis marmorata telangiectatica congenita | (Orphanet:1556) |
DIAMOND-BLACKFAN ANEMIA 10 | (OMIM:613309) |
DIGEORGE SYNDROME | (OMIM:188400) |
DISTICHIASIS WITH CONGENITAL ANOMALIES OF THE HEART AND PERIPHERALVASCULATURE | (OMIM:126320) |
DPM1-CDG | (Orphanet:79322) |
Dandy-Walker malformation - postaxial polydactyly | (Orphanet:1566) |
Deafness - onychodystrophy | (Orphanet:3231) |
Deafness-craniofacial syndrome | (Orphanet:3241) |
Desmosterolosis | (Orphanet:35107) |
Developmental delay-microcephaly-facial dysmorphism syndrome, Hutterite type | (Orphanet:363444) |
Diabetic embryopathy | (Orphanet:1926) |
Diffuse neonatal hemangiomatosis | (Orphanet:2123) |
Dislocation of the hip - dysmorphism | (Orphanet:2412) |
Distal 22q11.2 microduplication syndrome | (Orphanet:261337) |
Distal 7q11.23 microdeletion syndrome | (Orphanet:254351) |
Distal monosomy 10q | (Orphanet:96148) |
Distal monosomy 17q | (Orphanet:1597) |
Distal monosomy 6p | (Orphanet:96125) |
Distal trisomy 14q | (Orphanet:1705) |
Dysmorphism - short stature - deafness - disorder of sex development | (Orphanet:2282) |
Ebstein malformation | (Orphanet:1880) |
Ehlers-Danlos syndrome with periventricular heterotopia | (Orphanet:82004) |
Ehlers-Danlos syndrome, kyphoscoliotic and deafness type | (Orphanet:300179) |
Emanuel syndrome | (Orphanet:96170) |
FEINGOLD SYNDROME 1 | (OMIM:164280) |
Fanconi anemia | (Orphanet:84) |
Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3 | (Orphanet:168566) |
Feingold syndrome | (Orphanet:1305) |
Focal dermal hypoplasia | (Orphanet:2092) |
Glaucoma - ectopia - microspherophakia - stiff joints - short stature | (Orphanet:2084) |
Goldblatt syndrome | (Orphanet:166272) |
Goldenhar syndrome | (Orphanet:374) |
Gorlin-Chaudhry-Moss syndrome | (Orphanet:2095) |
Grange syndrome | (Orphanet:79094) |
HAJDU-CHENEY SYNDROME | (OMIM:102500) |
HETEROTAXY, VISCERAL, 1, X-LINKED | (OMIM:306955) |
HETEROTOPIA, PERIVENTRICULAR, X-LINKED DOMINANT | (OMIM:300049) |
HIRSCHSPRUNG DISEASE, CARDIAC DEFECTS, AND AUTONOMIC DYSFUNCTION | (OMIM:613870) |
HUNTER-MACDONALD SYNDROME | (OMIM:611962) |
HYPERTELORISM AND TETRALOGY OF FALLOT | (OMIM:239711) |
Heart defect - tongue hamartoma - polysyndactyly | (Orphanet:1338) |
Hereditary orotic aciduria | (Orphanet:30) |
Holt-Oram syndrome | (Orphanet:392) |
Hydrocephaly - low insertion umbilicus | (Orphanet:2184) |
Hypermethioninemia encephalopathy due to adenosine kinase deficiency | (Orphanet:289290) |
Hypertelorism, Teebi type | (Orphanet:1519) |
Hypertrichotic osteochondrodysplasia, Cantu type | (Orphanet:1517) |
Hypomandibular faciocranial dysostosis | (Orphanet:1790) |
Hypoplastic left heart syndrome | (Orphanet:2248) |
Hypoplastic left heart syndrome 2 | (OMIM:614435) |
INTESTINAL PSEUDOOBSTRUCTION, NEURONAL, CHRONIC IDIOPATHIC, X-LINKED | (OMIM:300048) |
Idiopathic neonatal atrial flutter | (Orphanet:45452) |
Intellectual deficit, X-linked - craniofacioskeletal syndrome | (Orphanet:163979) |
Intellectual deficit, X-linked, Armfield type | (Orphanet:85276) |
Intellectual disability-feeding difficulties-developmental delay-microcephaly syndrome | (Orphanet:363611) |
Intellectual disability-seizures-hypotonia-ophthalmologic-skeletal anomalies syndrome | (Orphanet:369837) |
Isotretinoin-like syndrome | (Orphanet:2306) |
Juvenile polyposis syndrome | (Orphanet:2929) |
KAGAMI-OGATA SYNDROME | (OMIM:608149) |
Kapur-Toriello syndrome | (Orphanet:2328) |
Klippel-Trénaunay syndrome | (Orphanet:90308) |
Knobloch syndrome | (Orphanet:1571) |
LOEYS-DIETZ SYNDROME 1 | (OMIM:609192) |
LOEYS-DIETZ SYNDROME 2 | (OMIM:610168) |
Lateral meningocele syndrome | (Orphanet:2789) |
Left ventricular noncompaction 1 | (OMIM:604169) |
Leprechaunism | (Orphanet:508) |
Lethal Kniest-like dysplasia | (Orphanet:2347) |
Lethal faciocardiomelic dysplasia | (Orphanet:1972) |
Lethal polymalformative syndrome, Boissel type | (Orphanet:210144) |
Lethal restrictive dermopathy | (Orphanet:1662) |
Loeys-Dietz syndrome type 1 | (Orphanet:60030) |
Lowry-MacLean syndrome | (Orphanet:2409) |
Lung agenesis - heart defect - thumb anomalies | (Orphanet:1120) |
Lymphedema - atrial septal defects - facial changes | (Orphanet:86915) |
Lymphedema - distichiasis | (Orphanet:33001) |
MENTAL RETARDATION, AUTOSOMAL DOMINANT 32 | (OMIM:616268) |
MESOAXIAL HEXADACTYLY AND CARDIAC MALFORMATION | (OMIM:249670) |
MICROPHTHALMIA, SYNDROMIC 9 | (OMIM:601186) |
MULTISYSTEMIC SMOOTH MUSCLE DYSFUNCTION SYNDROME | (OMIM:613834) |
Marshall-Smith syndrome | (Orphanet:561) |
Matthew-Wood syndrome | (Orphanet:2470) |
McKusick-Kaufman syndrome | (Orphanet:2473) |
Meacham syndrome | (Orphanet:3097) |
Meckel syndrome | (Orphanet:564) |
Meckel syndrome, type 1 | (OMIM:249000) |
Microcephalic osteodysplastic primordial dwarfism type 2 | (Orphanet:2637) |
Microcephaly - seizures - intellectual deficit - heart disease | (Orphanet:2519) |
Microphthalmia - microtia - fetal akinesia | (Orphanet:2547) |
Monosomy 18q | (Orphanet:1600) |
Monosomy 22q13 | (Orphanet:48652) |
Monosomy 9p | (Orphanet:261112) |
Mosaic trisomy 9 | (Orphanet:99776) |
Mowat-Wilson syndrome | (Orphanet:2152) |
Mulibrey nanism | (Orphanet:2576) |
Multifocal atrial tachycardia | (Orphanet:3282) |
Multiple congenital anomalies - hypotonia - seizures syndrome | (Orphanet:280633) |
Myhre syndrome | (Orphanet:2588) |
NOONAN SYNDROME 1 | (OMIM:163950) |
Nager syndrome | (Orphanet:245) |
Natal teeth - intestinal pseudoobstruction - patent ductus | (Orphanet:1654) |
Neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome | (Orphanet:457185) |
Neonatal hemochromatosis | (Orphanet:446) |
Nephronophthisis 16 | (OMIM:615382) |
Nephronophthisis 3 | (OMIM:604387) |
Nephronophthisis 9 | (OMIM:613824) |
Neu-Laxova syndrome | (Orphanet:2671) |
Neuroectodermal syndrome, Johnson type | (Orphanet:2316) |
Nodular neuronal heterotopia | (Orphanet:2149) |
Noonan syndrome | (Orphanet:648) |
Oculofaciocardiodental syndrome | (Orphanet:2712) |
Okamoto syndrome | (Orphanet:2729) |
Opitz G/BBB syndrome | (Orphanet:2745) |
Osteopathia striata - cranial sclerosis | (Orphanet:2780) |
PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER) | (OMIM:214100) |
PHACE syndrome | (Orphanet:42775) |
Pacman dysplasia | (Orphanet:1952) |
Pallister-Hall syndrome | (Orphanet:672) |
Pancreatic hypoplasia - diabetes - congenital heart disease | (Orphanet:2255) |
Patent arterial duct | (Orphanet:706) |
Patent ductus arteriosus - bicuspid aortic valve - hand anomalies | (Orphanet:228190) |
Pentasomy X | (Orphanet:11) |
Progressive retinal dystrophy due to retinol transport defect | (Orphanet:352718) |
Prune belly syndrome | (Orphanet:2970) |
RENAL-HEPATIC-PANCREATIC DYSPLASIA 1 | (OMIM:208540) |
RIGHT PULMONARY ARTERY, ANOMALOUS ORIGIN OF, FAMILIAL | (OMIM:610338) |
ROBERTS SYNDROME | (OMIM:268300) |
Recombinant 8 syndrome | (Orphanet:96167) |
Renal-hepatic-pancreatic dysplasia | (Orphanet:294415) |
Roberts syndrome | (Orphanet:3103) |
Rubinstein-Taybi syndrome due to CREBBP mutations | (Orphanet:353277) |
SENER SYNDROME | (OMIM:606156) |
SOTOS SYNDROME 1 | (OMIM:117550) |
Short rib-polydactyly syndrome, Beemer-Langer type | (Orphanet:93268) |
Short stature - wormian bones - dextrocardia | (Orphanet:2863) |
Short-rib thoracic dysplasia 13 with or without polydactyly | (OMIM:616300) |
Simpson-Golabi-Behmel syndrome | (Orphanet:373) |
Smith-Lemli-Opitz syndrome | (Orphanet:818) |
Sotos syndrome | (Orphanet:821) |
Split hand - urinary anomalies - spina bifida | (Orphanet:2437) |
Tetrasomy 12p | (Orphanet:884) |
Thanatophoric dysplasia | (Orphanet:2655) |
Thanatophoric dysplasia type 1 | (Orphanet:1860) |
Thanatophoric dysplasia type 2 | (Orphanet:93274) |
Timothy syndrome | (Orphanet:65283) |
Toriello-Carey syndrome | (Orphanet:3338) |
Townes-Brocks syndrome | (Orphanet:857) |
Transaldolase deficiency | (Orphanet:101028) |
Transketolase deficiency | (ORPHA:488618) |
Treacher-Collins syndrome | (Orphanet:861) |
Trisomy 13 | (Orphanet:3378) |
Trisomy 17p | (Orphanet:261290) |
Trisomy 1q | (Orphanet:261344) |
VACTERL/VATER association | (Orphanet:887) |
VENTRICULAR SEPTAL DEFECT 3 | (OMIM:614432) |
Van Regemorter-Pierquin-Vamos syndrome | (Orphanet:3419) |
WEILL-MARCHESANI SYNDROME 1 | (OMIM:277600) |
Weill-Marchesani syndrome | (Orphanet:3449) |
Williams syndrome | (Orphanet:904) |
X-linked lissencephaly with abnormal genitalia | (Orphanet:452) |
Zellweger syndrome | (Orphanet:912) |
Zimmermann-Laband syndrome | (Orphanet:3473) |