Congenital septal defect
Symptom Information:
Symptom ID: | HPO:0004760 | |||||||||
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) Abnormality of the cardiac septa(HPO:0001671) Congenital septal defect(HPO:0004760) MedDRA: |
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Database Frequency: | 69 / 7739 | |||||||||
Resource: |
All diseases associated with this symptom:
1p36 deletion syndrome | (Orphanet:1606) |
1q21.1 microdeletion syndrome | (Orphanet:250989) |
1q44 microdeletion syndrome | (Orphanet:238769) |
8p23.1 microdeletion syndrome | (Orphanet:251071) |
Absent thumb - short stature - immunodeficiency | (Orphanet:2951) |
Arthrogryposis - renal dysfunction - cholestasis | (Orphanet:2697) |
Atrial septal defect - atrioventricular conduction defects syndrome | (Orphanet:1479) |
Atrioventricular defect - blepharophimosis -radial defects | (Orphanet:1352) |
Autosomal recessive amelia | (Orphanet:1027) |
Baller-Gerold syndrome | (Orphanet:1225) |
Brain-lung-thyroid syndrome | (Orphanet:209905) |
Cartilage-hair hypoplasia | (Orphanet:175) |
Choanal atresia - deafness - cardiac defects - dysmorphism | (Orphanet:1200) |
Complete atrioventricular canal | (Orphanet:1329) |
Congenital amegakaryocytic thrombocytopenia | (Orphanet:3319) |
Congenital laryngeal web | (Orphanet:2374) |
Congenital pericardium anomaly | (Orphanet:2846) |
Congenital pulmonary veins atresia or stenosis | (Orphanet:3188) |
Congenital pulmonary venous return anomaly | (Orphanet:3090) |
Diprosopia | (Orphanet:1681) |
Dislocation of the hip - dysmorphism | (Orphanet:2412) |
Distal monosomy 13q | (Orphanet:1590) |
Distal monosomy 17q | (Orphanet:1597) |
Ebstein malformation | (Orphanet:1880) |
Eng-Strom syndrome | (Orphanet:1937) |
Fanconi anemia | (Orphanet:84) |
Focal dermal hypoplasia | (Orphanet:2092) |
Fryns syndrome | (Orphanet:2059) |
Genito-palato-cardiac syndrome | (Orphanet:2075) |
German syndrome | (Orphanet:2077) |
Holoprosencephaly - postaxial polydactyly | (Orphanet:2166) |
Intellectual deficit - microcephaly - phalangeal - facial abnormalities | (Orphanet:3067) |
Intellectual deficit, Buenos-Aires type | (Orphanet:3079) |
Intellectual deficit, X-linked, Armfield type | (Orphanet:85276) |
Johanson-Blizzard syndrome | (Orphanet:2315) |
Kabuki syndrome | (Orphanet:2322) |
Kleefstra syndrome due to 9q34 microdeletion | (Orphanet:96147) |
Koolen-De Vries syndrome | (Orphanet:96169) |
Larsen-like osseous dysplasia - short stature | (Orphanet:2370) |
Laryngo-tracheo-esophageal cleft - pulmonary hypoplasia | (Orphanet:2005) |
Lowry-MacLean syndrome | (Orphanet:2409) |
Megalencephaly - polymicrogyria - postaxial polydactyly - hydrocephalus | (Orphanet:83473) |
Microcornea - corectopia - macular hypoplasia | (Orphanet:2535) |
Microphthalmia with linear skin defects syndrome | (Orphanet:2556) |
Myhre syndrome | (Orphanet:2588) |
Natal teeth - intestinal pseudoobstruction - patent ductus | (Orphanet:1654) |
Nephronophthisis 2 | (OMIM:602088) |
Nephronophthisis 3 | (OMIM:604387) |
Oculofaciocardiodental syndrome | (Orphanet:2712) |
Okamoto syndrome | (Orphanet:2729) |
Osteodysplasty, Melnick-Needles type | (Orphanet:2484) |
Otopalatodigital syndrome type 2 | (Orphanet:90652) |
PHACE syndrome | (Orphanet:42775) |
Pentasomy X | (Orphanet:11) |
Peters-plus syndrome | (Orphanet:709) |
Sotos syndrome | (Orphanet:821) |
Spondyloepimetaphyseal dysplasia with joint laxity | (Orphanet:93359) |
Syndactyly - telecanthus - anogenital and renal malformations | (Orphanet:140952) |
Thiamine-responsive megaloblastic anemia syndrome | (Orphanet:49827) |
Thrombocytopenia - Robin sequence | (Orphanet:3323) |
Thrombocytopenia - absent radius | (Orphanet:3320) |
Toriello-Carey syndrome | (Orphanet:3338) |
Townes-Brocks syndrome | (Orphanet:857) |
Tracheal agenesis | (Orphanet:3346) |
Triploidy | (Orphanet:3376) |
VACTERL/VATER association | (Orphanet:887) |
Van Regemorter-Pierquin-Vamos syndrome | (Orphanet:3419) |
Williams syndrome | (Orphanet:904) |
Wolf-Hirschhorn syndrome | (Orphanet:280) |