Tetralogy of Fallot
Symptom Information:
Symptom ID: | HPO:0001636 | |||||||||||||||||
Synonyms: |
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Cross references: |
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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) 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) |
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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) |