Patent ductus arteriosus

Symptom Information:

Symptom ID: HPO:0001643
Synonyms:
Ductus arteriosus [HPO:0001643]
Persistent arterial duct [HPO:0001643]
Persistent ductus arteriosus [HPO:0001643]
Patent ductus arteriosus (disorder) [Orphanet:34520]
Patent ductus arteriosus [Orphanet:34520]
Ductus arteriosus [OMIM:Ductus arteriosus]
Patent ductus arteriosus [OMIM:Patent ductus arteriosus]
Patent ductus arteriosus [MedDRA:10034130]
Ductus arteriosus patent [MedDRA:10034130]
Patent ductus arteriosis [MedDRA:10034130]
PDA [MedDRA:10034130]
Patent ductus arteriosis [OMIM:Patent ductus arteriosis]
Patent ductus arteriosus (1 patient) [OMIM:Patent ductus arteriosus (1 patient)]
Patent ductus arteriosus (2 patients) [OMIM:Patent ductus arteriosus (2 patients)]
Patent ductus arteriosus (in 1 reported case) [OMIM:Patent ductus arteriosus (in 1 reported case)]
Patent ductus arteriosus (in some patients) [OMIM:Patent ductus arteriosus (in some patients)]
Patent ductus arteriosus (less common) [OMIM:Patent ductus arteriosus (less common)]
Patent ductus arteriosus (male) [OMIM:Patent ductus arteriosus (male)]
Patent ductus arteriosus (rare) [OMIM:Patent ductus arteriosus (rare)]
Persistent ductus arteriosus (rare) [OMIM:Persistent ductus arteriosus (rare)]
Quality:
Cross references:
HPO:0011648 "Patent ductus arteriosus after birth at term" [Orphanet:34520]
Orphanet:34520 "Patent ductus arteriosus" [Orphanet:34520]
OMIM: "Ductus arteriosus" [OMIM:Ductus arteriosus]
OMIM: "Patent ductus arteriosus" [OMIM:Patent ductus arteriosus]
OMIM: "Patent ductus arteriosis" [OMIM:Patent ductus arteriosis]
OMIM: "Patent ductus arteriosus (1 patient)" [OMIM:Patent ductus arteriosus (1 patient)]
OMIM: "Patent ductus arteriosus (2 patients)" [OMIM:Patent ductus arteriosus (2 patients)]
OMIM: "Patent ductus arteriosus (in 1 reported case)" [OMIM:Patent ductus arteriosus (in 1 reported case)]
OMIM: "Patent ductus arteriosus (in some patients)" [OMIM:Patent ductus arteriosus (in some patients)]
OMIM: "Patent ductus arteriosus (less common)" [OMIM:Patent ductus arteriosus (less common)]
OMIM: "Patent ductus arteriosus (male)" [OMIM:Patent ductus arteriosus (male)]
OMIM: "Patent ductus arteriosus (rare)" [OMIM:Patent ductus arteriosus (rare)]
OMIM: "Persistent ductus arteriosus (rare)" [OMIM:Persistent ductus arteriosus (rare)]
UMLS:C0013274 "Patent ductus arteriosus" [Orphanet:34520]
Is a (Direct Parents):
HPO         Congenital malformation of the great arteries
MedDRA Vascular malformations and acquired anomalies
Orphanet obsolete Malformation of the heart and great vessels
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)
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)