Tetralogy of Fallot

Symptom Information:

Symptom ID: HPO:0001636
Synonyms:
Tetrology of fallot [HPO:0001636]
Tetralogy of Fallot (disorder) [Orphanet:34380]
Tetralogy of Fallot [Orphanet:34380]
Tetralogy of Fallot [OMIM:Tetralogy of Fallot]
Tetralogy of Fallot/trilogy of Fallot [Orphanet:34380]
Fallot's tetralogy [Orphanet:34380]
Fallot's tetralogy [MedDRA:10016193]
Fallot tetralogy [MedDRA:10016193]
Fallot tetralogy of [MedDRA:10016193]
Tetralogy of Fallot [MedDRA:10016193]
Tetralogy of Fallot (1/4 patients) [OMIM:Tetralogy of Fallot (1/4 patients)]
Tetralogy of Fallot (in some patients) [OMIM:Tetralogy of Fallot (in some patients)]
Tetralogy of Fallot (rare) [OMIM:Tetralogy of Fallot (rare)]
Tetralogy of Fallot (reported in 1 patient) [OMIM:Tetralogy of Fallot (reported in 1 patient)]
Fallot's trilogy [MedDRA:10064011]
Trilogy of Fallot [Orphanet:34380]
Fallot's trilogy (disorder) [Orphanet:34380]
Quality:
Cross references:
Orphanet:34380 "Tetralogy of Fallot/trilogy of Fallot" [Orphanet:34380]
OMIM: "Tetralogy of Fallot" [OMIM:Tetralogy of Fallot]
OMIM: "Tetralogy of Fallot (1/4 patients)" [OMIM:Tetralogy of Fallot (1/4 patients)]
OMIM: "Tetralogy of Fallot (in some patients)" [OMIM:Tetralogy of Fallot (in some patients)]
OMIM: "Tetralogy of Fallot (rare)" [OMIM:Tetralogy of Fallot (rare)]
OMIM: "Tetralogy of Fallot (reported in 1 patient)" [OMIM:Tetralogy of Fallot (reported in 1 patient)]
UMLS:C0039685 "Tetralogy of Fallot" [Orphanet:34380]
UMLS:C0041022 "Trilogy of Fallot" [Orphanet:34380]
Is a (Direct Parents):
MedDRA Multiple cardiac abnormalities congenital
HPO         Conotruncal defect
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)
                Conotruncal defect(HPO:0001710)
                   Tetralogy of Fallot(HPO:0001636)
MedDRA:
Congenital, familial and genetic disorders(MedDRA:10010331)
    Cardiac and vascular disorders congenital(MedDRA:10007510)
       Multiple cardiac abnormalities congenital(MedDRA:10028177)
          Tetralogy of Fallot(HPO:0001636)
Database Frequency: 104 / 7739
Resource:

All diseases associated with this symptom:

10q22.3q23.3 microduplication syndrome (Orphanet:276422)
16p13.11 microduplication syndrome (Orphanet:261243)
1p36 deletion syndrome (Orphanet:1606)
1q21.1 microduplication syndrome (Orphanet:250994)
22q11.2 deletion syndrome (Orphanet:567)
22q11.2 microduplication syndrome (Orphanet:1727)
3C syndrome (Orphanet:7)
8p23.1 microdeletion syndrome (Orphanet:251071)
8p23.1 microduplication syndrome (Orphanet:251076)
ADAMS-OLIVER SYNDROME 1 (OMIM:100300)
APLASIA CUTIS CONGENITA, RETICULOLINEAR, WITH MICROCEPHALY, FACIALDYSMORPHISM, AND OTHER CONGENITAL ANOMALIES (OMIM:300887)
Acro-cardio-facial syndrome (Orphanet:2008)
Acro-renal-ocular syndrome (Orphanet:959)
Adams-Oliver syndrome (Orphanet:974)
Alagille syndrome due to 20p12 microdeletion (Orphanet:261600)
Alagille syndrome due to a JAG1 point mutation (Orphanet:261619)
Aminopterin/methotrexate embryofetopathy (Orphanet:1908)
Atrial septal defect - atrioventricular conduction defects syndrome (Orphanet:1479)
Atrioventricular defect - blepharophimosis -radial defects (Orphanet:1352)
Autosomal recessive Robinow syndrome (Orphanet:1507)
CARPENTER SYNDROME 1 (OMIM:201000)
CHARGE syndrome (Orphanet:138)
COFFIN-SIRIS SYNDROME (OMIM:135900)
CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 3 (OMIM:614954)
CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 4 (OMIM:615779)
Cantrell pentalogy (Orphanet:1335)
Cardiocranial syndrome, Pfeiffer type (Orphanet:2872)
Carpenter syndrome (Orphanet:65759)
Cataract - intellectual deficit - anal atresia - urinary defects (Orphanet:1381)
Coffin-Siris syndrome (Orphanet:1465)
Congenital alveolar capillary dysplasia (Orphanet:210122)
Congenital pericardium anomaly (Orphanet:2846)
Congenital unilateral hypoplasia of depressor anguli oris (Orphanet:1166)
Conotruncal heart malformations (Orphanet:2445)
DIAMOND-BLACKFAN ANEMIA 7 (OMIM:612562)
DIGEORGE SYNDROME (OMIM:188400)
Diabetic embryopathy (Orphanet:1926)
Distal monosomy 6p (Orphanet:96125)
Dysmorphism - multiple structural anomalies (Orphanet:1780)
ECTRODACTYLY OF LOWER LIMBS, CONGENITAL HEART DEFECT, AND MICROGNATHIA (OMIM:601348)
FACIAL DYSMORPHISM WITH MULTIPLE MALFORMATIONS (OMIM:227255)
Fallot complex - intellectual deficit - growth delay (Orphanet:3304)
Fanconi anemia (Orphanet:84)
Fetal trimethadione syndrome (Orphanet:1913)
Frontonasal dysplasia (Orphanet:250)
Fryns syndrome (Orphanet:2059)
German syndrome (Orphanet:2077)
Goldenhar syndrome (Orphanet:374)
HYPERTELORISM AND TETRALOGY OF FALLOT (OMIM:239711)
Holoprosencephaly (Orphanet:2162)
Holoprosencephaly - radial heart renal anomalies (Orphanet:3186)
Hydrocephaly - low insertion umbilicus (Orphanet:2184)
Hypertelorism, Teebi type (Orphanet:1519)
Hypoplastic left heart syndrome 2 (OMIM:614435)
Isolated Dandy-Walker malformation (Orphanet:217)
Joubert syndrome 2 (OMIM:608091)
Juvenile polyposis syndrome (Orphanet:2929)
Kapur-Toriello syndrome (Orphanet:2328)
Kleefstra syndrome (Orphanet:261494)
Kleefstra syndrome due to 9q34 microdeletion (Orphanet:96147)
LEOPARD SYNDROME 3 (OMIM:613707)
Lymphedema - distichiasis (Orphanet:33001)
MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I (OMIM:210710)
MICROPHTHALMIA, SYNDROMIC 9 (OMIM:601186)
Matthew-Wood syndrome (Orphanet:2470)
McKusick-Kaufman syndrome (Orphanet:2473)
Meacham syndrome (Orphanet:3097)
Microcephalic osteodysplastic primordial dwarfism types 1 and 3 (Orphanet:2636)
Microcephaly - facio-cardio-skeletal syndrome, Hadziselimovic type (Orphanet:217026)
Microphthalmia with linear skin defects syndrome (Orphanet:2556)
Mowat-Wilson syndrome (Orphanet:2152)
Nager syndrome (Orphanet:245)
Neurodegeneration due to 3-hydroxyisobutyryl-CoA hydrolase deficiency (Orphanet:88639)
Neuroectodermal syndrome, Johnson type (Orphanet:2316)
Noonan syndrome (Orphanet:648)
PHACE syndrome (Orphanet:42775)
PROGEROID FACIAL APPEARANCE WITH HAND ANOMALIES (OMIM:602249)
Pancreatic hypoplasia - diabetes - congenital heart disease (Orphanet:2255)
Patent arterial duct (Orphanet:706)
Polysyndactyly - cardiac malformation (Orphanet:2934)
Porencephaly - cerebellar hypoplasia - internal malformations (Orphanet:2941)
Prune belly syndrome (Orphanet:2970)
Recombinant 8 syndrome (Orphanet:96167)
Renal tubular dysgenesis (Orphanet:3033)
Renpenning syndrome (Orphanet:3242)
Short stature - heart defect - craniofacial anomalies (Orphanet:1088)
Solitary median maxillary central incisor syndrome (Orphanet:2286)
Spondylometaphyseal dysplasia, 'corner fracture' type (Orphanet:93315)
Syndromic diarrhea (Orphanet:84064)
TARP syndrome (Orphanet:2886)
TESTICULAR ANOMALIES WITH OR WITHOUT CONGENITAL HEART DISEASE (OMIM:615542)
TETRALOGY OF FALLOT AND GLAUCOMA (OMIM:187501)
TRICHOHEPATOENTERIC SYNDROME 1 (OMIM:222470)
Tetralogy of Fallot (Orphanet:3303)
Thrombocytopenia - absent radius (Orphanet:3320)
Timothy syndrome (Orphanet:65283)
Townes-Brocks syndrome (Orphanet:857)
VACTERL/VATER association (Orphanet:887)
VELOCARDIOFACIAL SYNDROME (OMIM:192430)
Warsaw breakage syndrome (Orphanet:280558)
Williams syndrome (Orphanet:904)
Wolfram syndrome 1 (OMIM:222300)
Yunis-Varon syndrome (Orphanet:3472)
Zunich-Kaye syndrome (Orphanet:3474)