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Ventricular septal defect, muscular

DA: 15

Developmental anomaly information

Definition: VSDs are caused by embryologic malformations of the ventricular septum, there is a defect in the inferior muscular part of ventricular septum. The interventricular communication corresponds to the abnormal passage of blood between the two ventricles (generally from the left ventricle toward the right ventricle).

Synonyms:

VSD muscular
Interventricular communication,muscular

Developmental anomaly parent: (empty)	Topology: Human body > Thorax > Mediastinum > Heart and great vessels > Heart
System: Human body > Cardiovascular system > Heart	Developmental anomaly category: Malformation

Case records MDB101, MDB149, MDB153, MDB157, MDB251, MDB53, MDB440, MDB452, MDB515, MDB526, MDB4, MDB36, MDB257, MDB399, MDB389, MDB390, MDB391, MDB22, MDB401, MDB329, MDB412, MDB418

Links

Humpath: 5933

Observed in MDB cases

Observed in combinaisons (MDB)

Observed in malformative diseases (MDB)

() in cases MDB, MDB, MDB, MDB

Associated genes in profile

Associated genes in malformative diseases

Associated chromosomal diseases

Associated signaling pathways

Associated developmental anomalies

Here is the list of developmental anomalies associated with this developmental anomaly, based on the cases' information :

Facial dysmorphism 6.02% (13/216 anomalies), in cases MDB101, MDB53, MDB440, MDB452, MDB515, MDB36, MDB257, MDB399, MDB390, MDB391, MDB401, MDB329, MDB418
Intrauterine growth retardation, symmetric 4.63% (10/216 anomalies), in cases MDB101, MDB53, MDB452, MDB399, MDB389, MDB390, MDB391, MDB22, MDB329, MDB418
Low-set ears 3.7% (8/216 anomalies), in cases MDB101, MDB53, MDB515, MDB257, MDB399, MDB390, MDB22, MDB329
Lobulated, fused and horseshoe kidney 3.24% (7/216 anomalies), in cases MDB101, MDB157, MDB53, MDB440, MDB257, MDB399, MDB391
Placenta hypoplasia 2.78% (6/216 anomalies), in cases MDB101, MDB157, MDB452, MDB526, MDB22, MDB329
Pulmonary hypoplasia 2.78% (6/216 anomalies), in cases MDB149, MDB36, MDB389, MDB391, MDB22, MDB329
Coarctation of aorta, 2.31% (5/216 anomalies), in cases MDB101, MDB157, MDB251, MDB53, MDB391
Talipes equinovarus, bilateral 2.31% (5/216 anomalies), in cases MDB153, MDB257, MDB391, MDB401, MDB418
Triangular face 2.31% (5/216 anomalies), in cases MDB53, MDB452, MDB399, MDB390, MDB22
Overlapping fingers 1.85% (4/216 anomalies), in cases MDB101, MDB157, MDB399, MDB22
Micrognathia 1.85% (4/216 anomalies), in cases MDB101, MDB157, MDB257, MDB412
Clindodactyly of 5th finger, bilateral 1.85% (4/216 anomalies), in cases MDB149, MDB515, MDB4, MDB391
Single umblical artery (SUA)-Isolated 1.39% (3/216 anomalies), in cases MDB53, MDB391, MDB418
Transverse palmar crease, bilateral 1.39% (3/216 anomalies), in cases MDB440, MDB515, MDB4
Rocker-bottom feet 1.39% (3/216 anomalies), in cases MDB440, MDB515, MDB401
Aberrant right subclavian artery 1.39% (3/216 anomalies), in cases MDB440, MDB526, MDB22
Adrenal hypoplasia, fetal 1.39% (3/216 anomalies), in cases MDB440, MDB452, MDB526
Cystic hygroma 1.39% (3/216 anomalies), in cases MDB257, MDB391, MDB329
Tracheoesophageal fistula (TEF), and esophageal atresia, Type C 1.39% (3/216 anomalies), in cases MDB257, MDB22, MDB22
Arthrogryposis 1.39% (3/216 anomalies), in cases MDB257, MDB401, MDB329
Meckel diverticulum 0.93% (2/216 anomalies), in cases MDB101, MDB157
Mongoloid slope of the palpebral fissures 0.93% (2/216 anomalies), in cases MDB149, MDB515
Macroglossia 0.93% (2/216 anomalies), in cases MDB149, MDB4
Wide space between 1st and 2nd toes, bilateral 0.93% (2/216 anomalies), in cases MDB149, MDB401
Pulmonary artery hypoplasia 0.93% (2/216 anomalies), in cases MDB149, MDB418
Relative Microcephaly 0.93% (2/216 anomalies), in cases MDB251, MDB36
Clindodactyly of 5th finger, unilateral 0.93% (2/216 anomalies), in cases MDB53, MDB22
Flattened nose 0.93% (2/216 anomalies), in cases MDB440, MDB329
Posteriorly inclined and low-positioned ears 0.93% (2/216 anomalies), in cases MDB440, MDB418
Short neck 0.93% (2/216 anomalies), in cases MDB440, MDB329
Cleft palate, bilateral 0.93% (2/216 anomalies), in cases MDB452, MDB257
Hypertelorism 0.93% (2/216 anomalies), in cases MDB515, MDB257
Nonimmune hydrops fetalis (NIHF) 0.93% (2/216 anomalies), in cases MDB36, MDB257
Long philtrum 0.93% (2/216 anomalies), in cases MDB257, MDB329
Retrognathia 0.93% (2/216 anomalies), in cases MDB399, MDB391
Intestinal malrotation 0.93% (2/216 anomalies), in cases MDB399, MDB391
Prominent and pointed nose 0.93% (2/216 anomalies), in cases MDB390, MDB391
Dextrocardia, isolated 0.93% (2/216 anomalies), in cases MDB391, MDB418
Preauricular hamartoma 0.93% (2/216 anomalies), in cases MDB391, MDB391
Microcephaly 0.93% (2/216 anomalies), in cases MDB22, MDB329
Persistent left superior vena cava 0.93% (2/216 anomalies), in cases MDB22, MDB418
Polymicrogyria, focal 0.93% (2/216 anomalies), in cases MDB329, MDB329
Syndactyly of the feet , simple (webbed), bilateral 0.46% (1/216 anomalies), in case MDB101
Syndactyly of the feet , simple (webbed), unilateral 0.46% (1/216 anomalies), in case MDB101
Aortic valve atresia 0.46% (1/216 anomalies), in case MDB101
Turned-up nose 0.46% (1/216 anomalies), in case MDB101
Tetralogy of Fallot 0.46% (1/216 anomalies), in case MDB149
Broad nasal bridge 0.46% (1/216 anomalies), in case MDB149
Neck edema 0.46% (1/216 anomalies), in case MDB149
Dilatation of the ascending aorta, congenital 0.46% (1/216 anomalies), in case MDB149
Patent Foramen Ovale 0.46% (1/216 anomalies), in case MDB149
Persistent Ductus arteriosus 0.46% (1/216 anomalies), in case MDB149
Bicuspid pulmonary valve 0.46% (1/216 anomalies), in case MDB149
Microstomia 0.46% (1/216 anomalies), in case MDB157
Giant omphalocele 0.46% (1/216 anomalies), in case MDB53
hypoplasia of the rib 0.46% (1/216 anomalies), in case MDB53
Renal pelvis dilatation, unilateral 0.46% (1/216 anomalies), in case MDB53
Radial ray agenesis, unilateral 0.46% (1/216 anomalies), in case MDB53
Syndactyly, simple (webbed), fingers 0.46% (1/216 anomalies), in case MDB53
Large anterior fontanelle 0.46% (1/216 anomalies), in case MDB53
Short philtrum 0.46% (1/216 anomalies), in case MDB440
Gastroschisis 0.46% (1/216 anomalies), in case MDB440
Polydactyly,of the hand, postaxial 0.46% (1/216 anomalies), in case MDB440
Flexion contracture of the fingers 0.46% (1/216 anomalies), in case MDB440
dextro-Transposition of the great arteries 0.46% (1/216 anomalies), in case MDB440
Thymic hypoplasia 0.46% (1/216 anomalies), in case MDB440
Cleft lip, unilateral 0.46% (1/216 anomalies), in case MDB452
Persistent truncus arteriosus 0.46% (1/216 anomalies), in case MDB452
Low nasal bridge 0.46% (1/216 anomalies), in case MDB515
Narrow thorax 0.46% (1/216 anomalies), in case MDB526
Hypoplasia of the humerus, bilateral 0.46% (1/216 anomalies), in case MDB4
Thin upper lip 0.46% (1/216 anomalies), in case MDB36
Epicanthus 0.46% (1/216 anomalies), in case MDB36
Flat face 0.46% (1/216 anomalies), in case MDB36
Renal hypoplasia 0.46% (1/216 anomalies), in case MDB36
Dysplasia of deep nuclei (olive dysplasia) 0.46% (1/216 anomalies), in case MDB257
Hydrocephalus, Non-communicating 0.46% (1/216 anomalies), in case MDB257
Microphthalmia 0.46% (1/216 anomalies), in case MDB257
Frontal bossing 0.46% (1/216 anomalies), in case MDB257
Small mouth 0.46% (1/216 anomalies), in case MDB257
Hypogenesis of pyramidal tracts 0.46% (1/216 anomalies), in case MDB257
Stenosis of aqueduct of Sylvius 0.46% (1/216 anomalies), in case MDB257
Unilobate lung, bilateral 0.46% (1/216 anomalies), in case MDB257
Anotia 0.46% (1/216 anomalies), in case MDB391
Absence of diaphragm, left 0.46% (1/216 anomalies), in case MDB391
Pterygium colli 0.46% (1/216 anomalies), in case MDB391
Pectus excavatum 0.46% (1/216 anomalies), in case MDB391
Omphalocele 0.46% (1/216 anomalies), in case MDB22
Absence of innominate (brachiocephalic) vein 0.46% (1/216 anomalies), in case MDB22
Pena Shokeir syndrome , Type I 0.46% (1/216 anomalies), in case MDB401
Overlapping nose bones 0.46% (1/216 anomalies), in case MDB401
Camptodactyly, bilateral 0.46% (1/216 anomalies), in case MDB401
Dislocation of hip, unilateral 0.46% (1/216 anomalies), in case MDB401
Left vertebral artery aberration 0.46% (1/216 anomalies), in case MDB401
Holoprosencephaly, lobar 0.46% (1/216 anomalies), in case MDB329
Thalamic nuclei centrum medianum fusion 0.46% (1/216 anomalies), in case MDB329
Corpus callosum agenesis 0.46% (1/216 anomalies), in case MDB329
Hypogenesis of the Cerebellar Vermis 0.46% (1/216 anomalies), in case MDB329
Cerebellar hypoplasia 0.46% (1/216 anomalies), in case MDB329
Megacystis 0.46% (1/216 anomalies), in case MDB329
Hydronephrosis, congenital, bilateral 0.46% (1/216 anomalies), in case MDB329
Dilatation of ureter , bilateral, congenital 0.46% (1/216 anomalies), in case MDB329
Prominent upper lip 0.46% (1/216 anomalies), in case MDB329
Hydromyelia 0.46% (1/216 anomalies), in case MDB329
Micromelia, lower limb, unilateral 0.46% (1/216 anomalies), in case MDB329
Myelomeningocele, lumbosacral 0.46% (1/216 anomalies), in case MDB412
Bladder hypoplasia 0.46% (1/216 anomalies), in case MDB418
Multicystic renal dysplasia,bilateral 0.46% (1/216 anomalies), in case MDB418
Right aortic arch 0.46% (1/216 anomalies), in case MDB418
Ureter hypoplasia 0.46% (1/216 anomalies), in case MDB418
Unicorn Uterus 0.46% (1/216 anomalies), in case MDB418
Fallopian tube, absence of 0.46% (1/216 anomalies), in case MDB418
Cleft palate with cleft lip,bilateral, complete 0.46% (1/216 anomalies), in case MDB418

Terminology and coding

References

No reference related to Ventricular septal defect, muscular is available at the moment.

Last modified: 2008-12-16 19:20:15 by farideh

Created: 2008-02-15 00:00:00 by phsaw

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