Congenital septal defect

Symptom Information:

Symptom ID: HPO:0004760
Congenital septal defects [HPO:0004760]
Congenital septal defects [OMIM:Congenital septal defects]
Cardiac septal defect [MedDRA:10064021]
Heart septal defect [Orphanet:34440]
Congenital septal defect of heart (disorder) [Orphanet:34440]
Congenital septal defect (morphologic abnormality) [Orphanet:34440]
Cardiac septal defects (disorder) [Orphanet:34440]
Heart Septal Defects [Orphanet:34440]
Cardiac septal defect [Orphanet:34440]
Cross references:
Orphanet:34440 "Cardiac septal defect" [Orphanet:34440]
OMIM: "Congenital septal defects" [OMIM:Congenital septal defects]
UMLS:C0018816 "Heart Septal Defects" [Orphanet:34440]
Is a (Direct Parents):
HPO         Abnormality of the cardiac septa
Orphanet obsolete Malformation of the heart and great vessels
Is a (Whole tree): HPO:
    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)
Database Frequency: 69 / 7739

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)