Malformations.org - View a developmental anomaly

Talipes equinovarus, bilateral

DA: 11

Developmental anomaly information

Definition: (empty)

Developmental anomaly parent: Talipes equinovarus	Topology: Human body > Limbs > Lower limbs > Foot
System: Human body > musculoskeletal system.	Developmental anomaly category: Deformation

Case records MDB29, MDB50, MDB118, MDB75, MDB80, MDB88, MDB119, MDB93, MDB103, MDB104, MDB110, MDB112, MDB114, MDB115, MDB117, MDB141, MDB143, MDB153, MDB180, MDB181, MDB193, MDB194, MDB205, MDB209, MDB215, MDB219, MDB223, MDB241, MDB246, MDB254, MDB257, MDB266, MDB267, MDB274, MDB288, MDB310, MDB317, MDB322, MDB327, MDB331, MDB333, MDB337, MDB341, MDB344, MDB362, MDB363, MDB292, MDB370, MDB391, MDB393, MDB396, MDB401, MDB406, MDB417, MDB418, MDB428, MDB431, MDB445, MDB446, MDB464, MDB479, MDB480, MDB140, MDB150, MDB158, MDB244, MDB299, MDB306, MDB338, MDB5, MDB79, MDB238, MDB324, MDB328

Links

Humpath: 4167

Observed in MDB cases

Observed in combinaisons (MDB)

Observed in malformative diseases (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 :

Pulmonary hypoplasia 3.68% (25/680 anomalies), in cases MDB29, MDB50, MDB75, MDB103, MDB104, MDB114, MDB181, MDB209, MDB223, MDB246, MDB254, MDB266, MDB274, MDB322, MDB327, MDB333, MDB337, MDB391, MDB417, MDB150, MDB244, MDB306, MDB238, MDB324, MDB328
Facial dysmorphism 3.38% (23/680 anomalies), in cases MDB29, MDB50, MDB104, MDB112, MDB115, MDB193, MDB205, MDB215, MDB257, MDB266, MDB317, MDB327, MDB331, MDB391, MDB393, MDB401, MDB418, MDB431, MDB479, MDB480, MDB338, MDB5, MDB238
Intrauterine growth retardation, symmetric 3.38% (23/680 anomalies), in cases MDB80, MDB103, MDB115, MDB194, MDB215, MDB219, MDB223, MDB246, MDB254, MDB266, MDB274, MDB310, MDB322, MDB337, MDB391, MDB396, MDB418, MDB431, MDB480, MDB140, MDB158, MDB338, MDB79
Placenta hypoplasia 2.79% (19/680 anomalies), in cases MDB29, MDB119, MDB103, MDB110, MDB209, MDB215, MDB219, MDB223, MDB254, MDB266, MDB274, MDB310, MDB317, MDB322, MDB333, MDB396, MDB417, MDB140, MDB338
Low-set ears 2.65% (18/680 anomalies), in cases MDB29, MDB103, MDB112, MDB181, MDB205, MDB209, MDB215, MDB223, MDB257, MDB310, MDB327, MDB331, MDB362, MDB292, MDB428, MDB140, MDB150, MDB238
Hypertelorism 2.21% (15/680 anomalies), in cases MDB50, MDB104, MDB181, MDB193, MDB215, MDB257, MDB322, MDB331, MDB363, MDB393, MDB446, MDB479, MDB480, MDB338, MDB238
Potter deformity sequence 2.06% (14/680 anomalies), in cases MDB80, MDB103, MDB104, MDB110, MDB181, MDB209, MDB219, MDB223, MDB446, MDB150, MDB244, MDB299, MDB306, MDB324
Micrognathia 1.47% (10/680 anomalies), in cases MDB104, MDB209, MDB257, MDB274, MDB310, MDB317, MDB363, MDB479, MDB238, MDB324
Single umblical artery (SUA)-Isolated 1.47% (10/680 anomalies), in cases MDB115, MDB209, MDB215, MDB246, MDB322, MDB333, MDB391, MDB418, MDB428, MDB464
Short neck 1.47% (10/680 anomalies), in cases MDB215, MDB322, MDB331, MDB341, MDB363, MDB417, MDB428, MDB479, MDB140, MDB338
Microretrognathia 1.18% (8/680 anomalies), in cases MDB103, MDB181, MDB223, MDB322, MDB327, MDB331, MDB333, MDB292
Flattened nose 1.18% (8/680 anomalies), in cases MDB104, MDB193, MDB209, MDB223, MDB446, MDB140, MDB299, MDB324
Arthrogryposis 1.18% (8/680 anomalies), in cases MDB110, MDB193, MDB257, MDB337, MDB401, MDB406, MDB479, MDB238
Potter's facies 1.18% (8/680 anomalies), in cases MDB110, MDB209, MDB219, MDB223, MDB446, MDB150, MDB299, MDB324
Low nasal bridge 1.03% (7/680 anomalies), in cases MDB103, MDB181, MDB223, MDB331, MDB292, MDB338, MDB324
Clindodactyly of 5th finger, bilateral 1.03% (7/680 anomalies), in cases MDB215, MDB219, MDB331, MDB362, MDB391, MDB140, MDB324
Overlapping fingers 0.88% (6/680 anomalies), in cases MDB88, MDB143, MDB194, MDB322, MDB158, MDB238
Bladder hypoplasia 0.88% (6/680 anomalies), in cases MDB104, MDB181, MDB209, MDB310, MDB418, MDB446
Imperforate Anus 0.88% (6/680 anomalies), in cases MDB115, MDB141, MDB209, MDB246, MDB150, MDB306
Nonimmune hydrops fetalis (NIHF) 0.88% (6/680 anomalies), in cases MDB257, MDB333, MDB337, MDB446, MDB479, MDB328
Multicystic renal dysplasia,bilateral 0.74% (5/680 anomalies), in cases MDB29, MDB181, MDB215, MDB418, MDB150
Long philtrum 0.74% (5/680 anomalies), in cases MDB29, MDB257, MDB322, MDB150, MDB324
Neck edema 0.74% (5/680 anomalies), in cases MDB29, MDB310, MDB322, MDB292, MDB324
Broad nasal bridge 0.74% (5/680 anomalies), in cases MDB50, MDB104, MDB181, MDB215, MDB322
Cubital deviation of the hand, unilateral 0.74% (5/680 anomalies), in cases MDB80, MDB205, MDB479, MDB244, MDB299
Myelomeningocele, lumbosacral 0.74% (5/680 anomalies), in cases MDB88, MDB193, MDB194, MDB370, MDB396
Ventricular septal defect, muscular 0.74% (5/680 anomalies), in cases MDB153, MDB257, MDB391, MDB401, MDB418
Myelomeningocele,lumbosacral with hydrocephalus 0.74% (5/680 anomalies), in cases MDB180, MDB241, MDB288, MDB417, MDB445
Arnold-Chiari Type II malformation (CM II) 0.74% (5/680 anomalies), in cases MDB193, MDB288, MDB370, MDB417, MDB445
Toe hypoplasia, first, bilateral 0.74% (5/680 anomalies), in cases MDB246, MDB254, MDB310, MDB362, MDB150
Lobulated, fused and horseshoe kidney 0.74% (5/680 anomalies), in cases MDB257, MDB310, MDB391, MDB417, MDB306
Prominent and pointed nose 0.74% (5/680 anomalies), in cases MDB317, MDB327, MDB391, MDB428, MDB431
Retrognathia 0.59% (4/680 anomalies), in cases MDB50, MDB114, MDB391, MDB431
Sloping forehead 0.59% (4/680 anomalies), in cases MDB112, MDB322, MDB327, MDB324
Polysplenia 0.59% (4/680 anomalies), in cases MDB181, MDB322, MDB150, MDB5
Tonsillar herniation of the cerebellum 0.59% (4/680 anomalies), in cases MDB193, MDB288, MDB370, MDB445
Rocker-bottom feet 0.59% (4/680 anomalies), in cases MDB194, MDB205, MDB401, MDB479
Ventricular septal defect, membranous 0.59% (4/680 anomalies), in cases MDB205, MDB310, MDB331, MDB5
Triangular face 0.59% (4/680 anomalies), in cases MDB223, MDB317, MDB327, MDB431
Cystic hygroma 0.59% (4/680 anomalies), in cases MDB257, MDB337, MDB391, MDB5
Camptodactyly, bilateral 0.59% (4/680 anomalies), in cases MDB266, MDB322, MDB396, MDB401
Wide space between 1st and 2nd toes, bilateral 0.59% (4/680 anomalies), in cases MDB266, MDB267, MDB401, MDB150
Epicanthus 0.44% (3/680 anomalies), in cases MDB29, MDB341, MDB5
Thumb agenesis, unilateral 0.44% (3/680 anomalies), in cases MDB75, MDB115, MDB140
Right bilobate lung 0.44% (3/680 anomalies), in cases MDB93, MDB193, MDB215
Encephalocele, occipital 0.44% (3/680 anomalies), in cases MDB104, MDB181, MDB464
Microcephaly 0.44% (3/680 anomalies), in cases MDB104, MDB322, MDB150
Nephromegaly, bilateral 0.44% (3/680 anomalies), in cases MDB104, MDB181, MDB194
Ureter hypoplasia 0.44% (3/680 anomalies), in cases MDB104, MDB181, MDB418
Single transverse palmar crease, unilateral 0.44% (3/680 anomalies), in cases MDB117, MDB331, MDB341
Anencephaly 0.44% (3/680 anomalies), in cases MDB141, MDB464, MDB140
Cerebellar hypoplasia 0.44% (3/680 anomalies), in cases MDB181, MDB288, MDB310
Pulmonary artery hypoplasia 0.44% (3/680 anomalies), in cases MDB205, MDB246, MDB418
Cleft palate, median posterior 0.44% (3/680 anomalies), in cases MDB215, MDB337, MDB431
Coarctation of aorta, 0.44% (3/680 anomalies), in cases MDB219, MDB333, MDB391
Renal agenesis, unilateral 0.44% (3/680 anomalies), in cases MDB241, MDB446, MDB150
Osteogenesis imperfecta, Type II 0.44% (3/680 anomalies), in cases MDB254, MDB266, MDB292
Decreased skull bone mineralization 0.44% (3/680 anomalies), in cases MDB254, MDB266, MDB292
Bowing of long bones 0.44% (3/680 anomalies), in cases MDB266, MDB274, MDB292
Hypogenesis of the Cerebellar Vermis 0.44% (3/680 anomalies), in cases MDB288, MDB310, MDB445
Pleural effusion, fetal 0.44% (3/680 anomalies), in cases MDB333, MDB324, MDB328
Dilatation of ureter , bilateral, congenital 0.44% (3/680 anomalies), in cases MDB341, MDB5, MDB324
Transverse palmar crease, bilateral 0.44% (3/680 anomalies), in cases MDB362, MDB363, MDB5
Preauricular hamartoma 0.44% (3/680 anomalies), in cases MDB391, MDB391, MDB5
Exophthalmos, bilateral 0.44% (3/680 anomalies), in cases MDB393, MDB480, MDB140
Posteriorly inclined and low-positioned ears 0.44% (3/680 anomalies), in cases MDB418, MDB479, MDB324
Giant omphalocele 0.29% (2/680 anomalies), in cases MDB29, MDB158
vertebral bones and gracile ribs with multiple abnormalities 0.29% (2/680 anomalies), in cases MDB29, MDB150
Macrocephaly 0.29% (2/680 anomalies), in cases MDB50, MDB193
Diastrophic Dysplasia 0.29% (2/680 anomalies), in cases MDB50, MDB274
Limbs hypoplasia 0.29% (2/680 anomalies), in cases MDB50, MDB274
Polymicrogyria, focal 0.29% (2/680 anomalies), in cases MDB118, MDB181
Absence of diaphragm, left 0.29% (2/680 anomalies), in cases MDB119, MDB391
Scoliosis, congenital 0.29% (2/680 anomalies), in cases MDB119, MDB238
Ectopia cordis 0.29% (2/680 anomalies), in cases MDB119, MDB119
Fingers amputation 0.29% (2/680 anomalies), in cases MDB93, MDB112
overlapping skull bones 0.29% (2/680 anomalies), in cases MDB93, MDB406
Bone mineralization defect 0.29% (2/680 anomalies), in cases MDB93, MDB103
Placenta circumvallata 0.29% (2/680 anomalies), in cases MDB103, MDB244
Renal-hepatic-pancreatic dysplasia 0.29% (2/680 anomalies), in cases MDB104, MDB181
Hexadactyly, postaxial 0.29% (2/680 anomalies), in cases MDB104, MDB181
Renal agenesis, bilateral 0.29% (2/680 anomalies), in cases MDB110, MDB209
Flexion contracture of the fingers 0.29% (2/680 anomalies), in cases MDB114, MDB322
Gastroschisis 0.29% (2/680 anomalies), in cases MDB141, MDB480
Dysplasia of hip, unilateral, congenital 0.29% (2/680 anomalies), in cases MDB143, MDB246
Olfactory bulbs, absence of 0.29% (2/680 anomalies), in cases MDB181, MDB480
Cerebral ventriculomegaly 0.29% (2/680 anomalies), in cases MDB193, MDB445
Renal focal cystic dilatation of collecting tubules 0.29% (2/680 anomalies), in cases MDB194, MDB393
Arhinia 0.29% (2/680 anomalies), in cases MDB205, MDB480
Persistent left superior vena cava 0.29% (2/680 anomalies), in cases MDB209, MDB418
Pericardial effusion 0.29% (2/680 anomalies), in cases MDB209, MDB324
Micromelia 0.29% (2/680 anomalies), in cases MDB215, MDB266
Microphthalmia 0.29% (2/680 anomalies), in cases MDB215, MDB257
Unilobate lung, unilateral 0.29% (2/680 anomalies), in cases MDB215, MDB5
Corpus callosum agenesis 0.29% (2/680 anomalies), in cases MDB219, MDB445
Short umbilical cord 0.29% (2/680 anomalies), in cases MDB219, MDB480
Frontal bossing 0.29% (2/680 anomalies), in cases MDB223, MDB257
Narrow thorax 0.29% (2/680 anomalies), in cases MDB223, MDB464
Renal hypertropy, fetal, bilateral 0.29% (2/680 anomalies), in cases MDB254, MDB238
Small mouth 0.29% (2/680 anomalies), in cases MDB257, MDB479
Cleft palate, bilateral 0.29% (2/680 anomalies), in cases MDB257, MDB238
Tracheoesophageal fistula (TEF), and esophageal atresia, Type C 0.29% (2/680 anomalies), in cases MDB257, MDB5
Neuronal migration anomaly 0.29% (2/680 anomalies), in cases MDB267, MDB322
Cortical dysgenesis (CD), diffuse 0.29% (2/680 anomalies), in cases MDB267, MDB322
Brachydactyly 0.29% (2/680 anomalies), in cases MDB274, MDB362
Syndactyly of the feet , simple (webbed), unilateral 0.29% (2/680 anomalies), in cases MDB310, MDB322
Long umbilical cord 0.29% (2/680 anomalies), in cases MDB310, MDB150
Gothic palate 0.29% (2/680 anomalies), in cases MDB322, MDB479
Polydactyly of the hand, preaxial 0.29% (2/680 anomalies), in cases MDB322, MDB322
Wide space between 1st and 2nd toes, unilateral 0.29% (2/680 anomalies), in cases MDB322, MDB327
Overlapping toes 0.29% (2/680 anomalies), in cases MDB327, MDB5
Splenomegaly, congenital 0.29% (2/680 anomalies), in cases MDB333, MDB393
Syndactyly, simple (webbed), fingers 0.29% (2/680 anomalies), in cases MDB337, MDB238
Macroglossia 0.29% (2/680 anomalies), in cases MDB341, MDB5
Radial deviation of the hand, unilateral 0.29% (2/680 anomalies), in cases MDB344, MDB140
Limbs hypoplasia, lower extremities 0.29% (2/680 anomalies), in cases MDB370, MDB406
Dextrocardia, isolated 0.29% (2/680 anomalies), in cases MDB391, MDB418
Intestinal malrotation 0.29% (2/680 anomalies), in cases MDB391, MDB5
Pectus excavatum 0.29% (2/680 anomalies), in cases MDB391, MDB393
Hepatomegaly, fetal 0.29% (2/680 anomalies), in cases MDB393, MDB428
Pena Shokeir syndrome , Type I 0.29% (2/680 anomalies), in cases MDB401, MDB479
Dislocation of hip, unilateral 0.29% (2/680 anomalies), in cases MDB401, MDB431
Cleft palate with cleft lip,bilateral, complete 0.29% (2/680 anomalies), in cases MDB417, MDB418
Flattened occiput 0.29% (2/680 anomalies), in cases MDB417, MDB5
Large anterior fontanelle 0.29% (2/680 anomalies), in cases MDB428, MDB431
Ureter agenesis, unilateral 0.29% (2/680 anomalies), in cases MDB446, MDB150
Anencephaly facies 0.29% (2/680 anomalies), in cases MDB464, MDB140
Teratoma, cerebral 0.29% (2/680 anomalies), in cases MDB480, MDB480
Flat face 0.29% (2/680 anomalies), in cases MDB150, MDB5
Axillary pterygia, bilateral 0.29% (2/680 anomalies), in cases MDB150, MDB238
Retroplacental hemorrhage 0.29% (2/680 anomalies), in cases MDB150, MDB324
Ascites, fetal 0.29% (2/680 anomalies), in cases MDB324, MDB328
Foot edema 0.15% (1/680 anomalies), in case MDB29
Axillary pterygia,unilateral 0.15% (1/680 anomalies), in case MDB29
Tridactyly, unilateral 0.15% (1/680 anomalies), in case MDB29
Hitchhiker thumb 0.15% (1/680 anomalies), in case MDB50
Bowing of long bones of leg, congenital 0.15% (1/680 anomalies), in case MDB50
Dislocation of the radial head, congenital 0.15% (1/680 anomalies), in case MDB50
thumb abduction,bilateral, 0.15% (1/680 anomalies), in case MDB118
Hypoplasia of the humerus, unilateral 0.15% (1/680 anomalies), in case MDB75
Laparoschisis 0.15% (1/680 anomalies), in case MDB75
skin hamartoma 0.15% (1/680 anomalies), in case MDB75
Parietal pericardium, absence of 0.15% (1/680 anomalies), in case MDB119
Omphalocele 0.15% (1/680 anomalies), in case MDB119
Defects of the lower part of the sternum 0.15% (1/680 anomalies), in case MDB119
Pulmonary lobation anomalies 0.15% (1/680 anomalies), in case MDB119
Encircling of developing structures by strands of amnion without constriction 0.15% (1/680 anomalies), in case MDB93
Autosomal Recessive Polycystic Kidney Disease 0.15% (1/680 anomalies), in case MDB104
Meckel diverticulum 0.15% (1/680 anomalies), in case MDB110
Cleft palate with cleft lip (CLP), median 0.15% (1/680 anomalies), in case MDB112
Polydactyly of the foot 0.15% (1/680 anomalies), in case MDB112
Polyhydramnios 0.15% (1/680 anomalies), in case MDB114
Akinesia, fetal 0.15% (1/680 anomalies), in case MDB114
Crossed fused renal ectopia 0.15% (1/680 anomalies), in case MDB115
Constriction Ring Deformity of the upper limbs 0.15% (1/680 anomalies), in case MDB115
Encephalocele, parietal 0.15% (1/680 anomalies), in case MDB115
Absence of hand and finger(s) (unilateral) 0.15% (1/680 anomalies), in case MDB141
absence of radius, unilateral 0.15% (1/680 anomalies), in case MDB141
Dislocation of the knee, congenital, unilateral 0.15% (1/680 anomalies), in case MDB143
Periventricular heterotopia (PH) 0.15% (1/680 anomalies), in case MDB181
Deep gray nuclear malformations(the caudate nuclei, thalami,..) 0.15% (1/680 anomalies), in case MDB181
putamen nuclei absence 0.15% (1/680 anomalies), in case MDB181
Glial heterotopia, multi-focal 0.15% (1/680 anomalies), in case MDB181
Corticospinal tract absence 0.15% (1/680 anomalies), in case MDB181
Relative Macrocephaly 0.15% (1/680 anomalies), in case MDB193
Beaked midbrain 0.15% (1/680 anomalies), in case MDB193
Rachischisis 0.15% (1/680 anomalies), in case MDB193
Tetralogy of Fallot 0.15% (1/680 anomalies), in case MDB205
Pulmonary valve atresia 0.15% (1/680 anomalies), in case MDB205
Hypoplasia of ascending aorta 0.15% (1/680 anomalies), in case MDB205
Right ventricular hypertrophy 0.15% (1/680 anomalies), in case MDB205
Badly-hemmed ears 0.15% (1/680 anomalies), in case MDB205
Cleft palate with cleft lip, unilateral, complete 0.15% (1/680 anomalies), in case MDB205
wrist hyperextension, unilateral 0.15% (1/680 anomalies), in case MDB205
Ureter agenesis, bilateral 0.15% (1/680 anomalies), in case MDB209
Prostate hypoplasia 0.15% (1/680 anomalies), in case MDB209
Aberrant right subclavian artery 0.15% (1/680 anomalies), in case MDB209
Marginal subchorionic hematoma 0.15% (1/680 anomalies), in case MDB219
Bowing of femur, congenital 0.15% (1/680 anomalies), in case MDB223
Placental cysts 0.15% (1/680 anomalies), in case MDB223
Right atrium Enlargement 0.15% (1/680 anomalies), in case MDB246
Right ventricular hypoplasia 0.15% (1/680 anomalies), in case MDB246
Shortening (micromelia) of upper limb(s) 0.15% (1/680 anomalies), in case MDB246
Amelia of the upper limb, unilateral 0.15% (1/680 anomalies), in case MDB246
Renal hypoplasia 0.15% (1/680 anomalies), in case MDB246
Scrotal hypoplasia 0.15% (1/680 anomalies), in case MDB246
Cleft palate, bilateral, complete 0.15% (1/680 anomalies), in case MDB254
Dysplasia of deep nuclei (olive dysplasia) 0.15% (1/680 anomalies), in case MDB257
Hydrocephalus, Non-communicating 0.15% (1/680 anomalies), in case MDB257
Hypogenesis of pyramidal tracts 0.15% (1/680 anomalies), in case MDB257
Stenosis of aqueduct of Sylvius 0.15% (1/680 anomalies), in case MDB257
Unilobate lung, bilateral 0.15% (1/680 anomalies), in case MDB257
Communicating hydrocephalus 0.15% (1/680 anomalies), in case MDB267
Purkinje cell ectopia in the cerebellum 0.15% (1/680 anomalies), in case MDB267
Absence of the pyramid tracts, bilateral 0.15% (1/680 anomalies), in case MDB267
Subcortical band heterotopia. 0.15% (1/680 anomalies), in case MDB267
Lissencephaly, Type II 0.15% (1/680 anomalies), in case MDB267
Absence of Cajal-Retzius cell 0.15% (1/680 anomalies), in case MDB267
Cubital deviation of the hand, bilateral 0.15% (1/680 anomalies), in case MDB274
Lower limb hyperextension, Fetal 0.15% (1/680 anomalies), in case MDB322
Gracile ribs 0.15% (1/680 anomalies), in case MDB322
Scoliosis, dextroconvex, thoracic 0.15% (1/680 anomalies), in case MDB322
Hydrocephalus 0.15% (1/680 anomalies), in case MDB322
Absence of neuron differentiation in the basal nuclei. 0.15% (1/680 anomalies), in case MDB322
Small round skull 0.15% (1/680 anomalies), in case MDB322
Brachycephaly 0.15% (1/680 anomalies), in case MDB331
Pectus carinatum 0.15% (1/680 anomalies), in case MDB337
Periventricular Leukomalacia (PVL) 0.15% (1/680 anomalies), in case MDB337
Microstomia 0.15% (1/680 anomalies), in case MDB341
Subcapsular renal cyst, 0.15% (1/680 anomalies), in case MDB341
Anotia 0.15% (1/680 anomalies), in case MDB391
Pterygium colli 0.15% (1/680 anomalies), in case MDB391
Dolicocephaly 0.15% (1/680 anomalies), in case MDB393
Overlapping nose bones 0.15% (1/680 anomalies), in case MDB401
Left vertebral artery aberration 0.15% (1/680 anomalies), in case MDB401
Nasal hypoplasia 0.15% (1/680 anomalies), in case MDB417
Right aortic arch 0.15% (1/680 anomalies), in case MDB418
Unicorn Uterus 0.15% (1/680 anomalies), in case MDB418
Fallopian tube, absence of 0.15% (1/680 anomalies), in case MDB418
Brachydactyly of the toes 0.15% (1/680 anomalies), in case MDB428
Malformed ear 0.15% (1/680 anomalies), in case MDB431
Radial ray agenesis, unilateral 0.15% (1/680 anomalies), in case MDB431
Thumb hypoplasia,unilateral 0.15% (1/680 anomalies), in case MDB431
Wide space between 2nd and third fingers 0.15% (1/680 anomalies), in case MDB431
Syndactyly of the toes, complex, bilateral 0.15% (1/680 anomalies), in case MDB431
Scaphoid abdomen 0.15% (1/680 anomalies), in case MDB431
Absence of the Septum Pellucidum 0.15% (1/680 anomalies), in case MDB445
Multicystic renal dysplasia, unilateral 0.15% (1/680 anomalies), in case MDB446
Palpebral edema, bilateral 0.15% (1/680 anomalies), in case MDB446
Cystic dysplasia of the rete testis (CDT), bilateral 0.15% (1/680 anomalies), in case MDB446
ectopic adrenal, peripancreatic 0.15% (1/680 anomalies), in case MDB446
Googly eyes 0.15% (1/680 anomalies), in case MDB464
Eventration of the diaphragm 0.15% (1/680 anomalies), in case MDB464
Hypertrophy of the Thymus 0.15% (1/680 anomalies), in case MDB464
Placental hydrops 0.15% (1/680 anomalies), in case MDB479
Limb-body-wall complex syndrome 0.15% (1/680 anomalies), in case MDB480
Primordial iris 0.15% (1/680 anomalies), in case MDB480
Anophthalmos, bilateral 0.15% (1/680 anomalies), in case MDB480
Arhinencephaly 0.15% (1/680 anomalies), in case MDB480
Olfactory nerve, absence of, bilateral 0.15% (1/680 anomalies), in case MDB480
Clivus, absence of 0.15% (1/680 anomalies), in case MDB480
Posterior cranial fossa dismorphisme 0.15% (1/680 anomalies), in case MDB480
Rudimentary radius and ulna (unilateral) 0.15% (1/680 anomalies), in case MDB480
Oligodactyly 0.15% (1/680 anomalies), in case MDB480
Ambiguous genitalia 0.15% (1/680 anomalies), in case MDB150
Hand edema 0.15% (1/680 anomalies), in case MDB150
Persistent cloaca 0.15% (1/680 anomalies), in case MDB150
Malpositioned thumb, bilateral 0.15% (1/680 anomalies), in case MDB150
Bulbous nose 0.15% (1/680 anomalies), in case MDB244
Flexion contracture of knee 0.15% (1/680 anomalies), in case MDB306
Rectovesical fistula 0.15% (1/680 anomalies), in case MDB306
Cloacal dysgenesis sequence (CDS) 0.15% (1/680 anomalies), in case MDB306
Hydroureter, unilateral 0.15% (1/680 anomalies), in case MDB306
Bladder dilatation, fetal 0.15% (1/680 anomalies), in case MDB306
Megarectum 0.15% (1/680 anomalies), in case MDB306
Renal hypoplasia, unilateral 0.15% (1/680 anomalies), in case MDB306
Hydronephrosis, congenital, unilateral 0.15% (1/680 anomalies), in case MDB306
Mongoloid slope of the palpebral fissures 0.15% (1/680 anomalies), in case MDB338
Clindodactyly of 5th finger, unilateral 0.15% (1/680 anomalies), in case MDB338
Atrial Hypertrophy 0.15% (1/680 anomalies), in case MDB5
Fusion of the adrenal glands 0.15% (1/680 anomalies), in case MDB5
Microsplenia 0.15% (1/680 anomalies), in case MDB5
Lung agenesis, unilateral 0.15% (1/680 anomalies), in case MDB5
Bladder wall thickness 0.15% (1/680 anomalies), in case MDB5
Amnion nodosum 0.15% (1/680 anomalies), in case MDB5
Flexion contracture of upper limbs 0.15% (1/680 anomalies), in case MDB79
Hypoplasia and dysplasia of the kidney, bilateral 0.15% (1/680 anomalies), in case MDB324
Megacystis 0.15% (1/680 anomalies), in case MDB324
Renal pelvis dilatation, bilateral 0.15% (1/680 anomalies), in case MDB324
Radial deviation of the hand, bilateral 0.15% (1/680 anomalies), in case MDB328
Placenta villous fibrosis 0.15% (1/680 anomalies), in case MDB328

Terminology and coding

	WHO ICD-10: Q66.0

References

No reference related to Talipes equinovarus, bilateral is available at the moment.

Last modified: 2009-01-05 14:31:42 by farideh

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

<< Previous anomaly entry

Next anomaly entry >>